Biological Activities of Resveratrol against Cancer
Received Date: Apr 02, 2018 / Accepted Date: Apr 09, 2018 / Published Date: Apr 28, 2018
Resveratrol (RSV) is a polyphenolic compound naturally found in grapes, peanuts, and berries. Considerable research has been performed to determine the benefits of RSV against various human diseases, especially cancer. Despite numerous studies on the effect of RSV on cancer, correct understanding of its mechanism is still far from certainty. This review summarizes the recent results on the molecular mechanisms and pathways of actions of RSV against major cancers. According to investigations accomplished worldwide, RSV targets pathways such as cell cycle progression, autophagy, apoptosis, angiogenesis and invasion/metastasis to attenuate cancer progression mediated through PI3K/Akt/mTOR, Wnt, ROS, NF-κB, BAX/Bcl-2, AMPK, ERK, MAPK signaling pathway. Considering the sideeffects and data of clinical trials, RSV can be used for its maximum benefits in human diseases. Available published data provide strong clues on the impact of RSV on cancer management.
Keywords: Resveratrol; Gastric cancer; Esophageal cancer; Breast cancer; Lung cancer; Colon cancer
Resveratrol (trans-3,4,5-trihydroxystilbene, RSV) is a polyphenol that is naturally found in berries, peanuts, and grapes and is produced in response to mechanical injury, fungal infection, and ultraviolet radiation . The concentration of RSV is 32 ng/g in blueberries, 1,920 ng/g in peanuts, and 3,540 ng/g in grapes [2,3]. Polygonum cuspidatum, a Japanese plant, was found to have the highest level of natural RSV and used for several ailments including inflammation . In 1997, Jang first demonstrated that external application of RSV prevented tumorigenesis in skin cancer model mice; thereafter, numerous investigations followed . Compared to high-fat diet, supplemental RSV showed beneficial effects and provided more energy in animal models [6-8]. Several publications have shown that RSV had multiple anticancer effects, such as protection against tumor initiation and cancer progression, apoptosis, antioxidant, anti-angiogenesis, anti-inflammatory, and antitumor migration [9-12]. In further investigations, application of RSV on the skin surface of mouse models of skin tumorigenesis revealed healing of the ailments by inducing apoptosis, controlling the cell cycle, and hindering COX activity [9-11]. One major disadvantage of RSV is its bioavailability, which has been proven to be less than 1 mg/ml . Therefore, various strategies have been used to enhance the solubility and bioavailability of RSV with the use of microparticles , cyclodextrin complexes , or nanoparticles [15,16] RSV has been found to possess potent antioxidant properties of ROS inhibition, AMPK activation, and suppression of lipid peroxidation . Oxidative stress is the result of alteration of balance between ROS production and consumption by antioxidant activity .
Moreover, RSV has been reported to protect different animal models against atherogenesis  and enhanced vasodilation by increasing the activity of endothelial nitric oxide synthase . Another study on a pig model revealed that RSV could prevent cardiovascular diseases by enhancing myocardial perfusion and decreasing oxidative stress . According to studies in the last decade, RSV exhibited neuroprotective  antidiabetic , radioprotective and cytogenetic  characteristics. Importantly, RSV has been reported to be effective in cancer . The anti-tumor effect of RSV is linked with its ability to regulate reactive oxygen species and cellular processes such as apoptosis, and both cancerous cell proliferation and differentiation. Therefore, in this review, we focus on the characteristics of RSV and molecular mechanism involved in the therapeutic role of RSV against cancers which, because of a wide spectrum of biological activities may be used in the prevention of cancer. We have summarized the regulation of cell cycle regulation, invasion/metastasis, angiogenesis and induced apoptosis and autophagy mediated through the regulated cell cycleassociated proteins; induced BCL-2/BAX and AMPK; inhibited the PI3K/Akt/Mtor, WNT, MEK, ERK pathways by resveratrol in different cancers. We have discussed the importance of these signaling pathways in cancer progression, along with their modulation by RSV.
Resveratrol and head and neck cancer
Head and neck cancer is the sixth most common cancer and is the eighth leading cause of death in the world . An in vitro study on human head and neck cancer cells revealed that RSV downregulated various STAT-3-related gene expressions and inhibited proliferation, invasion, and cell cycle arrest, including apoptosis, through induction of SOCS-1 mRNA and protein . Another investigation showed that combination of RSV and curcumin inhibited in vitro and in vivo cancer growth by increasing PARP cleavage and BAX/BCL-2 ratio and by inhibiting ERK1 and ERK2 phosphorylation . Moreover, RSV treatment was shown to inhibit cell viability, induce apoptosis of C666-1 cells by cleavage of caspase-3, and regulate Bax/BCL2 apoptotic signaling through activation of AMPK activity . In an in vitro study on human nasopharyngeal cancer, RSV treatment upregulated caspase-3 protein, but downregulated the expressions of BCL-2 and hypoxia-inducible factor-1alpha (HIF-1 alpha) protein and decreased the phosphorylation of Akt1, p70S6K, p-4EBP1, and cell cycle regulatory proteins to inhibit cancer progression . In a study on nasopharyngeal carcinoma cells HT1376 and Hep3B, RSV was reported to inhibit cell survival and have anti-apoptotic mechanisms by suppressing NP63 expression; these suggested that NP63, not P53, was a molecular target of RSV . RSV decreased cell growth and increased chemo- and radiosensitivity including cancer invasion of head and neck squamous cell carcinoma (HNSCC) cells which illustrated the anticancer property of RSV is mediated through regenerating gene (REG) III expression pathway . Feng treated Pterostilbene, a dimethylated resveratrol to human esophageal squamous cancer (EC109) cells and observed its anticancer effects such as decrease in cell viability, adhesion, migration and caspase-3 activity and increase in endoplasmic reticulum stress (ERS) related molecules (such as GRP78, ATF6, p-PERK, p-eI2F-alpha and CHOP) and concluded that the anticancer activity is due to the triggering of ERS signaling pathway . A study of oral squamous cell carcinoma showed that RSV significantly increased apoptosis and cell cycle arrest at G2/M phase of SCC-VII, SCC-25 and YD-38 cells in a dose- and time- dependent manner . In an oral cancer (SCC- 9) cells, RSV treatment prevented expression of MMP-9 protein, in addition to inhibition of the JNK1/2 and ERK1/2 signaling pathway . RSV proved to be cytotoxic by reducing cell migration ability and increasing cell cycle arrest and showed synergistic effect combined with irradiation in oral squamous cell carcinoma (PE/CA-PJ15) cells , also, an in vitro study showed that RSV inhibited adhesion, migration and invasion of OSCC cells . A study of human nasopharyngeal carcinoma cells showed that inhibiting autophagy by ATG7-siRNA and bafilomycinA1 increased the apoptotic cell death via increasing the endoplasmic stress and caspase-12 . In an research conducted in a C57BL/6 mice in which tongue tumorigenesis is induced by 4-nitroquinoline-1-oxide (4NQO) revealed that mice fed with grape seed extract or RSV had decreased tumor incidence compared to that of control through regulating AMPK activation thereby inducing apoptosis and autophagy . RSV is found to inhibit cell growth and promote cell differentiation in anaplastic thyroid carcinoma (ATC) cells by activating Notch1 signaling . Hu found that RSV suppressed invasiveness or anchorage independent growth of head and neck cancer cells regulated by several EMT markers in vitro and also reduced tumor growth in vivo in head and neck cancer mice model . RSV was found to inhibit cell growth, induce DNA damage and apoptosis in HNSCC cells independent of Smad4 expression in both in vivo and in vitro studies . Study of medullary thyroid (MTC) cancer showed that when RSV is treated to MTC cells, it suppressed cell growth via caspase-3 dependent apoptosis and decreased ASCL1 and chromogranin whereas induced Notch2 expression . A study showed that RSV induced apoptosis in human nasopharyngeal cancer cells by regulating multiple apoptotic pathways including death receptor, mitochondria and ER stress . In a study of UMSCC-22B cells, RSV was found to induce apoptosis and COX-2 accumulation in nucleus which leads to p53 activation and p53 dependent apoptosis . A study of thyroid cancer revealed that RSV treatment increase p53 expression and p53 dependent apoptosis via Ras-MAPK signaling pathway .
Resveratrol and esophageal cancer
A study in a Swedish population showed that a dietary pattern that included RSV might have a protective role in the development of esophageal cancer . Another research showed that RSV caused death of esophageal squamous cell carcinoma cells by inhibiting cell cycle progression at the sub G1 phase and by inducing apoptosis . Treatment of esophageal cancer cells- EC109 with pterostilbene, a RSV analog, reduced tumor cell adhesion, migration, and intracellular glutathione and increased the apoptotic index, caspase-3 activity, and ROS levels . In an F344 rat model of esophageal tumorigenesis induced by N-nitroso methyl benzylamine, oral and intraperitoneal RSV treatment at 2 mg/kg and 1–2 mg/kg, respectively, reduced the number of tumors by inhibiting COXs and prostaglandin E2 . Zhou showed that RSV inhibited the growth of EC-9706 in a doseand time-dependent manner through apoptosis by downregulating the expression of Bcl-2 gene and upregulating the expression of Baxgene . Another study showed that RSV suppressed esophageal adenocarcinoma cell proliferation by p27kip1 upregulation, which is controlled by downregulations of S-phase kinase-associated protein 2 and 26s proteasome . In a study, a group of 31 rats treated with RSV for 5 months reported decreased degree of esophagitis and incidence of intestinal metaplasia and carcinoma compared with the control group showing its chemo preventive property . Similarly, Szumilo also showed the chemopreventive property of RSV in rats that are exposed to chemical carcinogens .
Resveratrol and gastric cancer
Gastric cancer (GC) is the second most common cause of cancerassociated mortality  because it is difficult to be detected in the early phase. Since it is usually diagnosed in the advanced stages, prognosis is poor despite the availability of therapies such as surgery, chemotherapy, and radiotherapy . RSV can prevent Helicobacter pylori infection by inhibiting its growth. It also decreases oxidative stress by inhibiting H. pylori induced ROS production, which is a cause of cancer . In vivo studies on nude mice demonstrated that RSV administration to the site of tumor formation significantly inhibited both GC progression  and carcinoma growth via apoptotis . RSV reversed the doxorubicin resistant property of SGC7901/DOX cells back to doxorubicin sensitive cells which resulted to reduced migration/invasion, increased apoptosis in vitro and prevented tumor growth in vivo, moreover RSV inhibited AKT pathway to reverse the epithelial-mesenchymal transition (EMT) . Jing showed that RSV prevented gastric cancer cell growth by inhibiting cell cycle in MGC803 cells by suppressing PTEN/PI3K/AKT signaling pathway . The in vitro experiments performed by Gao revealed that RSV reduced invasion and metastasis in gastric cancer cells by hindering Hedgehog signaling pathway and EMT . In an in vitro study, RSV caused cell cycle arrest, induced apoptosis and reduced expression level of surviving inhibiting the proliferation of gastric cancer SGC7901 cells . When gastric cells were exposed to RSV in combination with dimethyl sphingosine (DMS) the cytotoxicity due to RSV accentuated depicting that inhibition of sphingolipid metabolism enhances RSV chemotherapy in human gastric cancer (SNU-1 and HT-29) cells . Further, Wang found that RSV caused increased production of ROS resulting in apoptosis and DNA damage in GC (SGC7901) cells while no effect was observed in sirtuin1 level . When gastric adenocarcinoma cells were treated with RSV, the number of micronuclei observed in the cells increased dose-dependently showing RSV’s genotoxic role . In a study of gastric cancer cells, RSV was found to mimic a role of dihydroceramide desaturase inhibitor which resulted in accumulation of dihydroceramide in cells that concluded that RSV ultimately induced autophagy via dihydroceramide in HGC-27 cells with no apoptosis . A study by Aquilano found that to suppress proliferation of human adenocarcinoma gastric cancer (AGS), trans-resveratrol inhibited phosphorylation of ERK1/2 via MEK1/2 ultimately repression of c-Jun activation . Moreover, RSV combined with garlic oil induced apoptosis via upregulation of Fas protein and bax gene and downregulation of bcl-2 gene . In another investigation, it was found that apoptotic signaling pathway of different cells of gastric adenocarcinoma cells responded differently to the treatment of RSV, for example, in SNU-1 cells, RSV downregulated survivin, however, activation of caspase-3 and cytochrome C oxidase activities was observed in AGS and KATO-III cells in response to RSV treatment . Similar research in gastric adenocarcinoma cells showed that RSV induced apoptosis and increased expression level of tumor suppressors p21 and p53 accompanied by cell cycle arrest at S to G(2)/M phases, the SNU-1 cells treated with RSV responded with upregulation of both Fas and Fas-L proteins, but p53 knocked out KATOIII cells showed elevated expression of Fas-L suggesting that RSV has chemopreventive properties against gastric adenocarcinoma cells via different approaches depending upon the cell type of the cancer . Additionally, inhibitory and chemopreventive effect of RSV against gastric adenocarcinoma (SNU-1) cells may be due to the ability of RSV to produce NO from NOS showing its antioxidant action . Atten investigated phosphotransferase activities of two key signaling enzymes- Protein kinase C (PKC) and mitogen-activated protein kinases (ERK1/2) in KATO-III and RF-1 cells, RSV induced cell cycle arrest, apoptosis and significantly inhibited PKC activity of KATO-III cells and of human recombinant PKC-alpha but no effect on ERK1/2 .
Resveratrol and colorectal cancer
Although the number of cases has declined owing to better detection and screening methods, colorectal cancer remains one of the leading causes of cancer deaths in western countries . Nutrition, food habit, and lifestyle substantially influence the development of colorectal cancer . A study found that RSV inhibited proliferation of colorectal cancer cells and diminished drug resistance by downregulating the NF-κB pathway and inhibiting epithelial-mesenchymal transition (EMT)-associated molecules, such as the mesenchymal marker vimentin and the transcription factor Slug, whereas upregulating the epithelial marker E-cadherin . RSV increased the phosphorylation and caused the proteasomal degradation of T-cell factor 4, resulting in the suppression of beta-catenin- and TCF-mediated transcriptional activity; these events increased apoptosis in human colorectal cancer cells . RSV extracted from Polygonum cuspidatum was reported to prevent invasion and metastasis of colorectal cancer cells by inhibiting the Wnt/beta-catenin signaling pathway through regulation of the expression of metastasis-associated lung adenocarcinoma transcript1 . RSV was shown to initiate endoplasmic stress, which eventually resulted in apoptotic death of colorectal cancer (HT 27) cells . Wolter found that RSV exhibited chemotherapeutic effect against colon cancer cells by cell cycle arrest through downregulation of the cyclinD1/CDK4 complex . Another study concluded that Sirt1 signaling pathway was one of the main mechanisms by which RSV exerted its effects on colorectal cancer cells . Karimi discovered that qRT-PCR and western blot analysis of LNA-anti0miR-200c transfected cells showed increased expression level of vimentin and ZEB-1 along with reduced expression level of E-cadherin which caused increase in the migration of HCT-116 cells but treatment of RSV reversed EMT to MET phenotype by upregulating mir-200c in colorectal cancer cells . Sonic hedgehog (Shh) protein increased the proliferation and migration rate of HCT-116 cells and increased expression level of Ptch, Smo and Gli-1 protein, but after treatment of RSV the cell viability and migration rate decreased via suppression of Ptch, Smo and Gli-1 protein level . A research by Feng demonstrated that RSV significantly inhibited cell proliferation of colon cancer cells (HCA-17, SW480, HT29) cells by inducing apoptosis and inhibiting expression of cyclooxygenase-2 and prostaglandin receptor . Yang found that RSV suppressed colorectal cancer by upregulating miR- 34c which successively was able to inhibit its target KITLG, this effect was accentuated in presence of p53 compared to p53-knockdown cells in vitro and in vivo . RSV significantly showed anti-cancer effect by upregulating expression level of BMP9 in LoVo cells, moreover, when p38 MAPK was inhibited, it partly reduced the anticancer effect of RSV but however anticancer effect was significantly lost by using BMPR inhibitor suggesting the anticancer property of RSV in LoVo cells is BMPR dependent . An interesting study regarding RSV dose-response relationship on a mice model of colorectal cancer found that low RSV dose repressed the cancer development more efficiently than 200 times higher dose by activating AMPK and upregulating the expression of the p21 protein . The colorectal cancer stem cells (CCSC) induced from HCT116 cells when treated with RSV resulted in decreased CCSC proliferation in a dose and time dependent manner, cell cycle arrest at G0/G1 phase and apoptosis including the upregulation of MICA/B expression to enhance cell immunogenicity . Demoulin showed that RSV inhibited cell growth progression of HCT-116 by inducing apoptosis, activating p53 and DNA damage via type-II topoisomerase poisoning . Clinical studies of colorectal cancer showed that RSV reduced cancer cell growth  by controlling the expression of WNT pathway target genes  and by increasing apoptosis in cancer tissues . Another study by Ji confirmed that RSV inhibited the migration and invasion of LoVo cells in a dose dependent manner by elevating the expression of E-cadherin and suppressing the expression of Vimentin, along with the inbition of TGF-beta1/smads signaling pathway . In an in-vivo study, mice fed with 150 - 300 ppm RSV demonstrated 60% inhibition of tumor production and in the remaining 40% of mice developed tumors which had lost Kras expression whereas in a therapeutic assay where mice had developed tumor showed complete disappearance of tumors in 33% of mice and 97% decrease in tumor size in remaining mice. In addition, RSV inhibited the expression of Kras expression which prevented the formation and growth of colorectal tumors . Another study found that RSV when treated in combination with mitomycin M enhanced the anticancer effects of MMC through upregulation of P21 (WAF1/ CIP1) causing the cell cycle arrest at G0/G1 and G2/M phases . Study on HCT116 and Caco-2 cells revealed that RSV induced cell cycle arrest and apoptosis via caspase dependent cyclin-CDK pathways . A study on colon cancer HCT116 cells showed that RSV hindered cell proliferation in vitro including in a xenograft tumor via upregulating expression of PTEN whereas decreasing phosphorylation of AKT, and the expression of protein and mRNA of beta-catenin are decreased by RSV in a dose dependent manner suggesting the involvement of WNT/beta-catenin pathway . A systematic study of activity of RSV on colorectal cancer cells – HCT116 and Caco-2 cells demonstrated an excellent anti-cancer property of RSV through downregulation of glycolytic enzymes, expression of leptin and c-Myc and content of vascular endothelial growth factor whereas the apoptotic markers were upregulated in the colorectal cancer cells which were calorie deprived suggesting that calorie restriction pathway may be the basis of the cell death . Miki H found that RSV increased intracellular reactive oxygen species (ROS) causing increase in autophagy that induced caspase dependent apoptosis in HT-29 and COLO 201 cells, suggesting that autophagy also mediated the apoptosis in human colon cancer cells . Study by Radhakrishnan found that RSV increased the apoptosis of colon cancer cells induced by grape seed extract through the apoptotic pathway involving P53 and Bax: bcl-2 ratio . Vanamala showed that proliferation of insulin like growth factor-1 (IGF-1) induced apoptosis via downregulation of IGF-1R/Akt/Wnt signaling pathways and by activation of P53, showing RSV’s anticancer effect . When RSV and tanninc acid is treated to Caco-2 cells, apoptotic index, Bak protein percentage ratio, and FADD protein % ratio values increased in a dose and time dependent manner inducing apoptosis in mitochondrial and death receptor pathways . A study of effect of RSV on HT-29 cells showed that RSV induced apoptosis via mitochondria apoptosis pathway triggered by production of ROS . Another in vitro study revealed that RSV caused apoptosis in human colon cancer cells (HT-29 and WiDr) in a dose-dependent manner including downregulation of telomerase activity (TLMA) in colon cancer cells . Interestingly, a study showed that RSV activated caspase-2 upstream of mitochondria which is not dependent upon anti-oxidant property of NF-kappaB inhibition but induced conformational changes in Bax/Bak with subsequent release of cytochrome-C, apoptosis-inducing factor, and endonuclease-G . Moreover, low concentration of RSV caused co-localization of Bax protein with mitochondria, collapse of mitochondrial membrane potential, activation of caspases resulting to apoptosis . The results of a study on SW480 show that RSV inhibited the cell growth by hindering cell cycle at S phase by accumulation of cyclin A and B1 along with CDK1 and CDK2 .
Resveratrol and liver cancer
Hepatocellular cancer is the sixth most common cancer and the second leading cause of cancer death . The major cause of hepatocellular cancer is infection with hepatitis B and hepatitis C virus. Diet and lifestyle were also considered as possible risk factors of liver cancer . A study reported that RSV inhibited the growth of HepG2 cells by decreasing the levels of cyclin D1, possibly by inhibiting the levels of p38 MAP kinases and the AKT pathway . Analysis of the cell cycle in liver cancer murine models showed that treatment with RSV at 10 and 15 mg/kg body weight significantly inhibited liver cancer by 36.3% and 49.3%, respectively by decreasing expression of cyclinB1 and p34cdc2 protein . A similar study on a murine model of liver cancer showed that RSV, in addition to 5-FU treatment, induced an S-phase arrest of H22 cell growth and enhanced the antitumor effects of chemotherapy . One research on HepG2 cells exposed to high glucose conditions to mimic a diabetic condition revealed that RSV (100 uM) suppressed the proliferation of HepG2 cells by inhibiting the STAT3 and Akt signaling pathways . Zhang found that RSV significantly decreased the proliferation of HepG2 cells and exerted its antitumor effect by suppressing the expression of the vascular endothelial growth factor (VEGF) gene . In an in vitro investigation of HepG2 hepatocellular carcinoma cells, a RSV analog known as phoyumbene B was found to be more effective than RSV in inhibiting cell proliferation by inducing G2/M cell cycle arrest and apoptosis by downregulating Bcl-2 and upregulating Bax, moreover, inhibition of invasion ability of the cells was also reported . A study showed significant anticancer activity when RSV was treated in combination with curcumin by caspase activation and upregulation of ROS . In a study the hepatocellular cancer (HCC) cells were found to have higher expression of Myosin light chain kinase (MLCK) but RSV treatment downregulated MLCK expression which triggered apoptosis and suppressed tumorigenesis suggesting MLCK might be linked with occurrence of HCC . High expression of urokinase (uPA) is correlated with high malignancy, in a study, RSV is reported to inhibit uPA expression and metastasis of HCC by downregulating transcription factors of SP-1 signaling pathway . In a rat hepatoma cell line, RSV was found to inhibit phosphorylation of mTOR and hence suppressing the protein synthesis to hinder liver cancer progression . Another study concluded that the anticancer property of RSV in HCC occurred due to upregulation of p-JNK expression while downregulation of p-ERK expression in vitro and in vivo . An investigation using male wistar rats revealed that administration of RSV at early or late stage of the liver cancer significantly decreased carcinogenesis via inducing apoptotic pathway . Weng investigated the effect of RSV and its analog on HCC and discovered the anti-invasive property of RSV which decreased protein expression of MMP-9 and MMP-2 while increased the expression of TIMP-1 and TIMP-2 . Bishayee discovered that treatment of RSV can inhibit hepatocarcinogenesis induced by diethylnitrosamine (DENA) in Sprague-Dawley rats by apoptotic pathway mediated through downregulation of BCL-2 and upregulation of Bax expression  similar study showed that RSV caused chemoprevention of hepatocarginogenesis by decreasing expression levels of heat shock protein (HSP70), COX-2 and NF-kappaB . Study by Yu HB concluded that RSV hindered growth of HepG2 cells by suppressing VEGF activity via inactivation of NF-kappaB, along with inhibition of tumor growth and angiogenesis . RSV inhibited cell growth of Huh-7 cells by downregulating cyclinE, cyclinA and CDK-2 while upregulating P21/WAF1 expression in a p53 dependent manner . Moreover, similar effect was seen in HepG2 cells line RSV inhibited growth of rat and human hepatoblastoma cells by restricting the cell cycle progression . Additionally, the synergistic effect of alcohol enhanced the cytotoxicity . The synergistic anti-cancer effect of RSV and 5-FU increased than compared to the each compound treated alone in hepatoma H22 cells . Yu found that RSV suppressed TNF-alpha dependent MMP-9 expression and invasion of HCC partly via downregulation of NF-kappaB signaling pathway . In a study, dietary RSV was found to have a hypolipidemic property along with anti-cancer and anti-metastatic effects against hepatoma in Donyu Rats . Another study of hepatoma showed the anti-invasive as well as anti-oxidative activity of RSV but no sign of inhibition of cell growth of hepatoma AH109A cells in vitro and ex vivo environment . In an investigation RSV is reported to reduce ROS production and inhibit cell growth through apoptosis and cell cycle arrest however it also increases iNOS, eNOS and hence increases NOS activity . A recent study revealed that a dimethylated derivative of RSV known as pterostilbene was able to induce caspase-3 and ROS dependent mitochondrial apoptotic pathway which resulted to inhibition of tumor progression in HCC . Study on HCC has discovered that RSV decreased hepatocyte growth factor-induced invasion of HepG2 cell invasion by an unknown mechanism . RSV suppressed proliferation of HCC cells in dose-dependent manner by inhibiting c-Met signaling pathway in vitro in addition to significant inhibition of tumor growth in vivo in a xenograft model .
Resveratrol and prostate cancer
Prostate cancer is the most common cancer in men and a major cause of cancer deaths . A study showed that RSV inhibited Akt, an upstream regulator of the miR-21 gene in PC-3M-MM2 cells, to reduce the viability and invasiveness of a tumor in vitro as well as in vivo . Another research found that RSV treatment reduced lipopolysaccharide-induced markers of EMT and inhibited the expression of Gli1; these findings showed the inhibitory effect of RSV on PC-3 and LNCaP cell lines . Moreover, RSV was reported to inhibit nuclear translocation of beta-catenin by decreasing HIF-1alpha expression, which leads to the suppression of tumor growth of castration-resistant prostate cancer . Ganapathy concluded that RSV was a potential drug for prostate cancer because it inhibited tumor growth, metastasis, and angiogenesis by enhancing the therapeutic efficacy of TRAIL through activation of the FOXO transcription factor . In addition, Benitez DA suggested that both the anti-proliferative and apoptotic effects of RSV on human prostate cancer cells were mediated by inactivation of NF-κB activity, which was associated with PI3K inhibition . RSV in combination with docetaxel when treated resulted to apoptosis and cell cycle arrest via upregulation of P53 expression and cell cycle inhibitors such as P21, WAF1, CIP1, and P27KIP in prostate cancer cells . In a study of murine model of prostate cancer, RSV was found to decrease cell viability, modify cell morphology and disrupt mitochondrial membrane potential leading to abnormal expression of Bax and Bcl2 protein but had no effect on caspase-3 . RSV is also found to reduce DDX5 (also known as P68) protein expression and cause cell death by inhibiting the mTORC1 pathway in prostate cancer cells . The research conducted by Selvaraj discovered that RSV triggered autophagic cell death in PC3 and DU145 cells by regulation of store operated calcium entry (SOCE) machinery in addition to downregulation of stromal interaction molecule 1 (STIM1) expression and induction of ER stress by decreasing ER calcium pool . Dhar revealed that RSV downregulated metastasis associated protein 1 (MTA1), a PTEN inhibitor thereby causing inhibition of AKT pathway and hence controlling prostate cancer progression . In LNCaP-FGC cells, when RSV treatment showed the inhibition of IL-6/DHT (Interlukin-6/dihydrotestosterone) induced androgen receptor (AR) transcriptional activity and partly mediated through suppression of STAT-3 reporter gene activity to hinder prostate cancer . RSV along with other wine polyphenols showed anti-proliferative effects and induction of apoptosis in LNCaP cells via reduced expression of androgen receptor (AR) and caspase -3-7 . Fang showed that RSV increased the sensitivity of melanoma cells to radiation by suppressing proliferation and inducing apoptosis . Another study demonstrated that RSV inhibited cancer cell growth by upregulation of superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX) expression and enzymatic activity which results in mitochondrial accumulation of H2O2 to finally induce apoptosis . In an investigation, RSV was found to possess a cytotoxic role in a dose and time dependent manner in prostate carcinoma (CWR22) cells in vitro but no effect in the in vivo study . In addition, RSV when used in combination with radiation therapy resulted to enhanced anti-proliferative effect through upregulation of p15, p21 and p53 and downregulation of cyclinB, cyclinD and cdk2 . Moreover, a study by Rashid A suggested that RSV causes cell cycle arrest, induces apoptosis and enhances the sensitivity of prostate cancer cells to ionizing radiation by modulating AMPK, Akt and mTOR signaling pathway . Harada discovered that RSV inhibited DNA binding of androgen receptor (AR), by decreasing the level of acetylation of AR and hence reducing the prostate cancer development . An investigation performed on prostate cancer by Chakraborty found that pterostilbene was able to suppress the cell growth factors like Akt, Bcl-2 and induce the mitochondrial apoptotic signals like Bax and caspases, and also inhibit MMP-9 and AMACR which are two metastasis markers [154,155]. A comparative study among RSV and its various analog compounds concluded that trans-RSV trimethyl ether was the most potent compound to treat prostate cancer (LNCaP) cells via cell cycle arrest and apoptosis . Shi demonstrated that RSV suppressed AR gene expression via inhibition of AR-transcriptional activity . Additional studies conducted by Kai confirmed that RSV downregulated MTA1 expression which destabilized the MTA1/NuRD complex which caused decrease in activation of P53 ultimately resulting to decrease in cell growth and activation of pro-apoptotic genes in prostate cancer cells . RSV inhibited proliferation of AR-positive hormone nonresponsive (CWR22Rv1) cells along with reduction of expression of NF-kappaB p65 via signaling pathway involving NQO2 protein . Gill discovered that RSV could sensitize androgen independent prostate cancer cells to apoptosis through multiple mechanisms such as Akt, Bax, IAPs in PC-3 cells and DU145 cells . Study of TRAILresistant LNCaP cells showed that RSV upregulated Bax, Bak, PUMA, NOXa, Bim and downregulated Bcl-2, Bcl-xL, XIAP and surviving and sensitized the cells along with activation of caspase-3 and caspase-9 which triggered apoptosis . In a study of transgenic adenocarcinoma mouse prostate males, the dietary RSV fed to the mouse revealed significantly decrease in cell proliferation, increase in androgen receptor, estrogen receptor-beta and insulin-like growth factor-1 receptor and insulin-like growth factor (IGF)-1 suggesting the suppression of prostate cancer development . A study by Benitez DA showed that RSV have anticancer property in both androgensensitive and androgen-non-sensitive human prostate tumors by inhibiting PI3K signaling pathway . Another study suggested that RSV caused sensitization of human prostate cancer (DU145) cells to ionizing radiation and accumulation of ceramide which is a potential mediator of anti-cancer activity induced by RSV . Aziz showed in their study that RSV caused suppression of PI3/AKT which caused modulation of Bcl-2 family protein to induce apoptosis of LNCaP cells . A study on an androgen –resistant human prostate cancer (DU145) cells revealed that RSV and proposis extract when treated caused cell death via necrosis and apoptosis respectively suggesting these micronutrient as an alternative to chemotherapy . Gao in their in vivo and in vitro research showed that RSV and genestein modulated AR function for chemopreventive effect via activation of Raf-MEK-ERK kinase pathway . Another investigation on prostate cancer cells found that RSV inhibited the proliferation of DU145 cells with a normal apoptotic mechanism besides suppressing the expression of heat shock proteins (HSPs70) . In a research conducted by Kim found that RSV when treated to human prostate cancer (DU145) cells resulted to cell growth inhibition and apoptosis in a dose-dependent manner via activation of caspase-3 and caspase-9 . A genetic analysis of LNCaP cells showed that RSV induced genes related to prostate cancer such as prostate specific antigen, AR co-activator ARA24 and NF-kappaB p65 which are associated with activation of p53 responsive genes- p53, p21, p300/CBP and Apaf-1 . Ding found that RSV inhibited cell growth by inducing cell cycle arrest at sub-G0/G1 cells and apoptosis in PANC-1 and AsPC-1 cells . Similarly, Morris found that RSV inhibited cell growth by inducing apoptosis in independent of the hormone responsive or unresponsive LNCaP cells . Another study on LNCaP cells showed that RSV inhibited the proliferation of the cells by arresting cell cycle at S phase and by inhibiting DNA synthesis . Additionally, RSV was found to suppress prostate specific antigen, human glandular kallikrein-2, AR-specific coactivator ARA70 and the CDKinhibitor p21 showing RSV as a potent therapeutic agent for prostate cancer . A study by Hsieh TC reported that RSV caused apoptosis of LNCaP and lowered prostate-specific antigen (PSA) levels which demonstrated the anticancer role of RSV against prostate cancer .
Resveratrol and pancreatic cancer
Pancreatic cancer is a fatal disease with a very poor prognosis with low survival rate due to late stage diagnosis of the cancer as most of the pancreatic cancer patients are asymptomatic until advanced stage of the disease . A study showed that RSV suppressed the development of ROS-induced pancreatic cancer by inhibiting hedgehog signaling proteins, which also suppressed the levels of uPA and MMP2 proteins . RSV induced apoptosis in capan 2 and colo 317 cells by activating caspase 3 and upregulated the protein expression of P53 and P21 in pancreatic cancer cells . Li showed that RSV not only inhibited cell growth, migration, and invasion, but also helped in the expression of EMT-related genes for metastasis through inhibition of the PI3/Akt/NF-kB signaling pathway . Another research revealed that different pancreatic cancer cells, such as PANC-1, BXPC-3, and ASPC-1, had different responses to RSV-induced apoptotic cell death by regulating the expression of caspases, Bcl-2, Bcl-xL, XIAP, and Bax . RSV treatment of human pancreatic cancer stem cells in Kras (G12D) mice inhibited growth and development of pancreatic cancer, caspase-dependent apoptosis, and inhibition of migration, invasion, and EMT . RSV suppressed ROS-induced pancreatic cancer progression by inhibiting the ERK and P38 MAPK signaling pathways . Furthermore, pterostilbene, a derivative of RSV, inhibited in vitro cell proliferation by caspase activation, mitochondrial membrane depolarization, and cell cycle arrest in pancreatic cancer . Zhu found that RSV when treated in combination with Metformin caused upregulation of Bax, cleaved-caspase3 and downregulation of Bcl-2 showed anti-cancer property in pancreatic cancer (Paca) cells . A study found that RSV inhibited cell growth and activated apoptosis by activation of AMPK and increased sensitivity to gemcitabine by inhibiting YAP expression in pancreatic cancer cells . In another study, RSV in combination with apocynin inhibited cell proliferation and arrested cell cycle progression at G1 phase with cyclin D1 downregulation and inactivation of Akt-GSk3beta and ERK1/2 in a human and hamster pancreatic cancer cells . Study of MIA PaCa-2 cells showed that RSV inhibited cell proliferation and colony formation by inducing apoptosis of MIA PaCa-2 cells along with the decreased level of Ihh, Ptch and Smo suggesting the inhibition of Hedgehog signaling pathway . In pancreatic cancer capan-2 cells, Yang. discovered that RSV acted as a tumor inhibitor via upregulation of Bax, however, it also induced tumorigenesis by upregulating VEGF-B, and hence, combinatorial effect of RSV and inhibitor of VEGF-B might be a favorable strategy for treatment of pancreatic cancer . RSV inhibited the cell viability of pancreatic cancer cells by inhibiting miR-21 which subsequently inhibited Bcl-2 expression resulting to apoptosis . In an investigation, RSV inhibited cell growth via induction of apoptosis through downregulation of downstream target proteins of Hedgehog pathway such as Gli1, Ptc1, CCND1 and BCL-2 in pancreatic cancer PANC-1 cells . Roy showed that when RSV was treated to pancreatic cancer cells, upregulation of p21/CIP1, p27/ kip1 and inhibition of cyclinD1 caused cell cycle arrest while activation of caspase-3 triggered apoptosis through inhibition of FOXO transcriptional activity dependent upon ERK and AKT pathway . In a study, RSV induced apoptosis including cell cycle arrest at S and G0/G1 phase through downregulation of AKT signaling in insulinoma INS-1E cells . Golkar reported that when RSV is treated to pancreatic cells, it showed a significant decrease in cell proliferation through upregulation of Macrophage inhibitory cytokine (MIC-1) gene indicating its key role in RSV induced anti-cancer property .
Resveratrol and lung cancer
Lung cancer is the most common cancer and a leading cause of cancer-associated mortality worldwide. The risk factors for lung cancer include cigarette smoking; indoor air pollution; chemicals such as polycyclic aromatic hydrocarbons; genetic factors such as chromosome abnormalities, mutations, and structural hydrocarbons; and diseaseassociated factors such as chronic obstructive pulmonary disease and chronic bronchitis . RSV has been reported to augment etoposideinduced cytotoxicity in human non-small cell lung cancer (NSCLC) cells by downregulating ERK1/2- and AKT-mediated expression of the X-ray Repair Cross-Complement Group-1 protein . A similar study on NSCLC showed that RSV enhanced the anticancer effect of cisplatin by inducing cell apoptosis and mitochondrial dysfunction . RSV has been proven to inhibit transforming growth factor (TGF)-β1-induced EMT, which is known to promote invasion and metastasis of carcinoma . A RSV analog 3,44ʹ-trihydroxy-transstilbene (10-80 μmol/L) inhibited cell viability of NSCLC, A549 cells, by inducing apoptosis, increasing acidic compartments in cells and LC3-II accumulation and GFP-LC3 labelled autophagosomes in the cells, also, the cell death accentuated when autophagy was inhibited by an autophagy inhibitors such as 3-methyladenine and wortmannin. In addition, it also elevated reactive oxygen species . RSV treatment sensitized NSCLC cells to radiotherapy by increasing ROS production and ionizing radiation-induced premature senescence .
Resveratrol and brain tumors
Glioblastoma is the most morbid form of brain tumor in adults and has poor prognosis . Lin showed that RSV strongly inhibited cell growth and induced apoptosis in A172 and T98G glioblastoma cells by activating Notch-1 and restoring wild-type P53 expression in a timeand dose-dependent manner . Another study indicated RSV as a potential anti-tumor agent for glioblastoma multiforme CD133+ cells, in vivo and in vitro, by inhibiting the self-proliferating capacity of the brain tumor, decreasing the invasion ability, and enhancing apoptosis by radiotherapy through suppression of the STAT3 pathway . Glioblastoma-initiating cells play significant roles in the onset, growth, and recurrence of glioblastoma multiforme. Although glioblastoma is highly resistant to temozolomide, addition of RSV enhanced the sensitivity of these glioblastoma-initiating cells to temozolomide and induced apoptosis through double-stranded DNA breaks, including an increase in differentiation of glioblastoma-initiating cells, through STAT3 inactivation . Further research has demonstrated that RSV inhibited cell proliferation, arrested the S-phase cell cycle, and induced apoptosis in vitro; it suppressed intracranial C6 tumor growth in vivo by significantly downregulating oncomiRs (miR21, miR30a-5p, and miR19) that target the p53, PTEN, EGFR, STAT3, COX-2, NF- κB, and PI3/Akt/mTOR pathways . An investigation by color Doppler ultrasound showed that RSV suppression of glioma growth was significantly dependent on the inhibition of macroscopic and microscopic angiogenesis . Zhang confirmed the YKL-40 gene as the most overexpressed gene in glioblastoma; RSV treatment suppressed YKL-40 expression in vitro and reduced the phosphorylation of ERK1/2 in a time-dependent manner . A study on c-Myc expression in medulloblastoma cells found that c-Myc downregulation by RSV was an important cause of suppression of medulloblastoma activity through growth inhibition, cell cycle arrest, and apoptosis of medulloblastoma tissues and cell lines (UW 229-2 and UW 228-3) . A recent study revealed that RSV was able to suppress cell proliferation, increase cell death and decrease cell motility by regulating WNT signaling pathway and EMT activators in Glioma Stem Cells . In a study of rat glioblastoma, RSV administered through lumbar puncture was found to significantly inhibit rat glioblastoma development via inactivation of STAT3 signaling pathway and by promoting autophagy and apoptosis . Clark found that RSV inhibited cell growth, invasion of U87 glioma and glioma stem-like cell and also suppressed glioblastoma xenograft growth by reducing AKT phosphorylation and by inducing P53 expression . A study on by Ryu demonstrated that RSV induced apoptosis and inhibited cell growth by increasing the expression of tristetraprolin in human glioma (U87MG) cells . In another study of human glioma cells, Yang discovered that RSV effectively inhibited the expression of pokemon to enhance cell apoptosis, senescence and antiproliferation induced by RSV . A study on glioma stem cells (GSCs), RSV was found to reduce selfrenewal and tumor-initiating ability of GSCs by inhibiting Nanog via activating P53/P21 pathway . Study of glioma (C6) cells by Figueiro showed that nanocapsulation of RSV enhanced the therapeutic action of RSV in vitro as well as in vivo by initiating cell cycle arrest and apoptosis compared to normal solution of RS. Research by Wang C reported that RSV inhibited proliferation of GH3 cells by inducing G0/ G1 cell cycle arrest and apoptosis and decreasing prolactin production . Lin CJ found that combination of RSV and temozolomide caused decrease of growth of tumor by suppressing ROS/ERK-mediated autophagy and apoptosis in glioma cells . In an in vitro and in vivo investigation, RSV was found to induce senescence of glioma cells and caused cell growth inhibition by suppressing mono-ubiquitination of histone H2B at K120 (uH2B) . In a study of U87MG cells, RSV was able to suppress the growth of malignant glioblastoma by inhibiting expression of nestin but by increasing expression of glial acidic fibrillary and betaIII-tubulin in time dependent manner . Another study showed that RSV induced cell cycle arrest at S phase with an increase in histone H2AX phosphorylation in human glioblastoma cells by inhibiting recombinant human TOPO II alpha to decatenate kDNA which act as TOPO II poison . Li revealed that RSV induced autophagy in human U251 glioma cells and autophagy played protective role and hence concluded that autophagy inhibitor can increase the efficacy of RSV to suppress the proliferation of glioma cells . A study of CD133+ cells derived from teratoid/rhabdoid tumor revealed that RSV inhibited cell proliferation, induced apoptosis and increased radiosensitivity as a therapeutic effect to the brain tumor . Additionally, RSV initiated neuronal differentiation of medulloblastoma cells and suppressed expression and phosphorylation of STAT3 along with its downstream genes such as survivin, cyclinD1, COX-2 and c-Myc and in UW228-2 and UW228-3 cells .
Resveratrol and breast cancer
Although breast cancer has a decreasing incidence, it remains the second leading cause of cancer deaths in women in the US . The treatment strategies available for breast cancer are chemotherapy, radiation, and surgical resection of tumors; hormonal therapy may also be given for post-menopausal women . Khan showed that RSV treatment induced breast cancer cell apoptosis by downregulating FASN and HER2 genes synergistically. Additionally, RSV attenuated PI3K/Akt/mTOR pathway signaling by downregulating Aktphosphorylation and upregulating PTEN expression . RSV treatment reduced the expression of β-catenin and cyclin-D1 in vitro and in vivo . Another study showed that RSV significantly enhanced doxorubicin-induced death of multidrug-resistant breast cancer cells in vitro and decreased 60% of the tumor volume under similar in vivo conditions . Rsv or triacetyl-Rsv induced cell cycle arrest and apoptosis and initiated P53 activation in MCF-7 and MDAMB231 breast cancer cells to control the cancer cell proliferation . In an experimental rat model of mammary tumor, Chatterjee showed that daily dietary supplement of 0.001% RSV for 24 weeks increased apoptosis and decreased DNA damage, cell growth, and levels of 5-lipoxygenase, TGF-β1, and NF-κB .
Resveratrol and skin cancer
RSV has been shown to initiate senescence in human A431 squamous cell carcinoma cells by blockade of its autolysosome form and downregulation of Rictor protein expression, resulting in alteration of cytoskeleton and suppression of skin cancer progression . A study on a mouse model of skin tumor concluded that RSV regulated apoptosis and cell survival by upregulating P53 and Bax, downregulating BCL-2 and surviving expressions, and regulating the PI3K/AKT pathway . An in vitro and an in vivo study of skin cancer revealed that the synergistic effect of RSV and 5-FU caused cell cycle arrest of TE-1 and A431 cancer cells at S-phase, as well as apoptosis with increased protein levels of p53, cleaved caspase-3, cleaved PARP, and Bax/Bcl-2 ratio . Moreover, topical application of RSV (25 μM) on the skin significantly reduced tumorigenesis in the mice . Kim demonstrated that oral administration of RSV significantly suppressed ultraviolet-induced skin tumorigenesis in p53 (+/-)/SKH- 1 mice that were highly tumor-susceptible through an Akt-mediated downregulation of TGF-β2 . RSV suppressed the development of human skin squamous cell carcinoma A431 cells in nude mice through a caspase-3-dependent apoptotic pathway and by downregulation of protein expression of surviving . After multiple exposures of SKH-1 nude mice model to ultraviolet B, RSV was topically applied on the skin; immunoblot and immunohistochemical analysis revealed that the anti-proliferative property of RSV was mediated through the modulation of important cell cycle regulatory proteins, probably through inhibition of the MAPK pathway. RSV decreased the viability of immortalized human keratinocytes by dephosphorylation of Akt and phosphorylation of ERK1/2, which is linked to the induction of p66Shc-Ser36 phosphorylation .
Resveratrol and leukemia
Chronic myelogenous leukemia (CML) is a cancer of the white blood cells that occurs due to a reciprocal translocation between chromosomes 9 and 22 . Wu discovered that treatment with RSV (20–100 μM) induced apoptosis and phosphorylation of histone H2AX in CML K562 cells through regulation of P38 and JNK, which are associated with the MAPK pathway . When acute lymphoblastic leukemia (ALL) CCRF-CEM cells were treated with RSV, there was dose-dependent cell death along with upregulation of miR16-1 and miR15a expressions, as analyzed by real-time polymerase chain reaction . A study concluded that RSV inhibited proliferation of T-cell ALL cells by inducing cell cycle arrest, apoptosis, and autophagy through suppression of the Akt/mTOR/p70s6k/4E-BP1 pathway and activation of the P38-MAPK signaling pathway . Human CML K562 cells treated with imatinib mesylate in combination with RSV were shown to have a significant decrease in cell viability and increased apoptosis, compared to the treatment with imatinib mesylate alone . In a study, hydroxylated RSV analogs were reported to induce cell death, accompanied by loss of mitochondrial potential, oxidative stress, loss of superoxide dismutase activity, and increased activity of caspase-3 and caspase-9 . Yaseen showed that RSV in combination with histone deacetylase inhibitors induced cell death through generation of ROS, activation of an extrinsic apoptotic pathway, and induction of DNA damage, including upregulation of death receptor-5 . Furthermore, RSV combined with arsenic trioxide induced apoptosis, mitochondrial damage, and oxidative stress in acute promyelocytic leukemia; RSV also prevented cardiotoxicity caused by arsenic trioxide .
Harmful effects/side-effects of Resveratrol
There are numerous studies that indicated RSV as an anticancer therapeutic agent, but some studies have mentioned the negative effects of RSV. RSV has been reported to downregulate PTEN-mRNA expression and upregulate BCL-xL mRNA expression, causing proliferation and survival of liver cancer HepG2 cells . Another study stated that after oral administration to the animal models, RSV accumulated in various internal organs, especially in the heart, liver, kidneys, and stomach . Another limitation of RSV is its poor bioavailability, which precludes its significant healing functions . A trial suggested that by regulating circulatory function in the brain, RSV could improve mood and cognition and reduce the possibility of dementia in post-menopausal women and in other populations at risk . RSV has been shown to have beneficial effects in high-fat diet and obesity; however, it increased the expression of fasting-induced adipogenic factor in the intestines of mice fed a high-fat diet and accelerated the progression of obesity . Roberts found that RSV use in pregnancy caused an unexplained variation in fetal pancreatic development; this study warned about RSV administration to pregnant women . In a study of eight healthy subjects who received 2 g RSV twice per day for eight days, six suffered mild episodic diarrhea and one developed rash and headache . In long-term studies of 24 months in rats and 18 months in mice, chronic exposure to RSV at a daily dose of less than 1g/kg had no adverse effects (7); on the other hand, oral intake of more than 3 g/kg per day resulted in neuropathy, renal toxicity, and liver toxicity in a group of rats [249,250].
Clinical trials on Resveratrol
The first clinical trial on the effect of RSV in eight patients with colon cancer demonstrated that low-dose RSV inhibited WNT signaling in normal colonic mucosa, indicating its beneficial role in colon cancer prevention . A clinical trial on middle-aged men with metabolic syndrome showed that the daily intake of high-dose RSV (1000 mg) for four months decreased the serum levels of androgen precursors, but there were no changes in prostate size, PSA level, and testosterone level; these suggested that RSV has no beneficial effects in prostate cancer . In a study involving six patients with liver cancer, three patients consumed placebo and another three consumed RSV (5000 mg/day) for 10–21 days before surgery. In RSV-administered patients, RSV was detected in hepatic tissues and the apoptotic marker cleaved-caspase-3 increased by 39%; however, no effect was observed in well-known markers of cancer, such as Akt, ERK, beta-catenin, JNK, surviving, or BCL-2 . Another study revealed that 12-week supplementation with 500 mg RSV reduced ALT and hepatic steatosis in patients with NAFLD, but there was no effect on blood pressure, insulin resistance markers, and lipid profile . In 119 participants who were randomly given oral placebo or RSV 500 mg daily for 52 weeks, RSV was observed to penetrate the blood-brain barrier and was measurable in plasma and CSF; the adverse effects were nausea, diarrhea, and weight loss . A clinical trial of two weeks of high-dose RSV reduced intestinal and hepatic lipoprotein production; however, long-term studies are required to verify the potential clinical benefits of RSV in patients with increased level of triglyceride-rich lipoproteins . A randomized, double-blind, placebo-controlled, parallel-group study on 60 adults aged 18–30 years showed that single-dose RSV intake for 28 days significantly decreased the subjective ratings of fatigue .
Various studies have shown that RSV has promising therapeutic effects on different cancers (Figures 1-3). Increasing number of studies on RSV provides insights into the molecular pathways and mechanisms of action of the RSV on cancer. In this review, we summarize the recent studies of RSV on the molecular mechanisms and pathways of actions against major cancers (Table 1) RSV inhibited cell cycle regulation, invasion/metastasis, angiogenesis and induced apoptosis and autophagy mediated through the regulated cell cycleassociated proteins; induced BCL-2/BAX and AMPK; inhibited the PI3K/Akt/Mtor, WNT, MEK, ERK pathways. However, the side-effects or harmful effects of RSV should be considered before administration. Only few human clinical trials have shown beneficial effects of RSV in diseases, but several have shown a neutral effect, probably due to its low bioavailability. Therefore, further active experimental research on RSV can give us a deeper understanding of its therapeutic effects on cancer.
Figure 3: Various therapeutic effects of resveratrol. Multiple signaling pathways associated with human cancers including head and neck, esophageal, gastric, colorectal, liver, prostate, pancreatic, lung, brain, breast, skin, and leukemia cancers are regulated by resveratrol in the process of apoptosis, DNA damage, cell death, Wnt, Erk, and Akt signaling pathway. Black arrows indicate activation cascade, while red lines indicate the inhibition cascade by resveratrol.
|Cancer||Effect of Resveratrol||References|
|Inhibition of STAT3, cell cycle||[27,29,33,35]|
|Head and neck cancer||Activation of AMPK, apoptosis||[28,30,32,38,42,44,45]|
|Regenerating gene expression|||
|JNK1/2 and ERK1/2 signaling|
|ER stress, autophagy||[37,43]|
|Inhibition of migration/ invasion||[36,40]|
|DNA damage/Smad 4 signaling|||
|Cell cycle arrest at G1-phase||[46,47]|
|Esophageal cancer||Increase apoptosis|||
|Inhibition of COXs and PG (E2)|||
|Inhibition of BCL-2 and increase in BAX|||
|Inhibition of P27kip1(CDK inhibitor)|||
|Cell cycle arrest at G1-phase||[59,61,67,71]|
|Gastric cancer||Antioxidant action, autophagy, metabolism||[62,63,65,70]|
|Induction of apoptosis||[57,66,68,69]|
|Inhibition of migration/invasion||[58,60]|
|Inhibition of NF-κB and EMT|||
|Colorectal cancer||Inhibition of invasion/metastasis||[76,80,81,91]|
|Activation of ER-stress and apoptosis||[77,89,90,98-101,103,104]|
|Cell cycle arrest and cyclid-D1/CDK4 complex||[78,83,85,86,92-94,105]|
|Sirt1 and p38 MAPK signaling pathway||[79,84]|
|Wnt/beta catenin signaling pathway||[95,96]|
|Downregulation of telomerase activity|||
|Inhibition of cyclin-D1, MAPK, and cell cycle||[108,109,110,113,124,125]|
|Liver cancer||Inhibition of STAT3and Akt|||
|Inhibition of angiogenesis/metastasis||[112,116,120,121,123,127]|
|Inhibition of invasion||[128,129,133]|
|Inhibition of Met signaling||[132,134]|
|Inhibition mTOR and ERK||[116-118]|
|Decrease COX-2 and NFkB|||
|Inhibition of AKT/EMT||[136,137,164]|
|Inhibition of AKT/EMT||[136,137,164]|
|Prostate cancer||Inhibition of beta-catenin/HIF1-alpa|||
|Inhibition of metastasis/angiogenesis||[139,144,145,154]|
|Inhibition of NF-κB and PI3K/ apoptosis||[140,142,149,155,157,159]|
|Cell cycle arrest||[141,150,151,152,170,172]|
|Reduce androgen receptor||[147,148,153,156,158,161]|
|Modulate androgen receptor function||[162,165,166,169,174]|
|Accumulation of ceramide|||
|Inhibition of uPA and MMP2, invasion|||
|Pancreatic cancer||Increase P53 and P21, cell cycle arrest||[182,185,190,191]|
|Inhibition of PI3K/Akt/NF-kB|||
|Inhibition of BCL-2 and increase in BAX||[179,183]|
|Inhibition of P38 and MAPK|||
|Inhibition of Hedgehog signaling pathway||[186,189]|
|Inhibition of ERK1/2|||
|Lung cancer||Increase apoptosis and mitochondrial dysfunction|||
|Inhibition of invasion/metastasis|||
|Increase ROS and autophagy||[197,198]|
|Induction of apoptosis||[16,200,210,211,214,219]|
|Inhibition of STAT3 and invasion||[201,202]|
|Cell cycle arrest at S-phase||[203,206,211,213,217]|
|Brain cancer||Inhibition of angiogenesis and invasion/metastasis||[204,209]|
|Inhibition of YKL-40 and ERK1/2|||
|Inhibition of WNT signaling and EMT|||
|Inactivation of STAT3 signaling pathway/ autophagy||[208,218,220]|
|Inhibition of Nanog via activation of p53/p21|||
|Suppressed histone H2B at K120 and nestin||[215,216]|
|Breast cancer||Downregulation of PI3K/Akt/Mtor|||
|Reduced beta catenin and cyclin D1|||
|Cell cycle arrest|||
|Decreased DNA damage|||
|Inhibition of Rictor|||
|Upregulation of P53 and Bax/ apoptosis||[229,230,233]|
|Skin cancer||Inactivation of AKT and Erk1/2||[232,234]|
|Cell cycle arrest by inhibition of MAPK pathway|||
|Induction of apoptosis||[236,239,240]|
|Upregulation ofmiR16-1 and miR15a|||
|Leukemia||Activation of P38/MAPK|||
|DNA damage, ROS activation||[241,242]|
Table 1: Summary of the therapeutic effects of resveratrol in various cancers.
Conflict of Interest
No potential conflicts of interest relevant to this article are reported.
This research was supported from the Medical Research Center Program (NRF-2017R1A5A2015061) through the by the National Research Foundation of Korea (NRF), which is funded by the Korean government (MISP) and by the Basic Science Research Program (2015R1C1A2A01054054).
- Langcake P, Pryce RJ (1976) The production of resveratrol by Vitis vinifera and other members of the Vitaceae as a response to infection or injury. Physiological Plant Pathology 9: 77-86.
- Sanders TH, McMichael RW (2000) Occurrence of resveratrol in edible peanuts. J Agric Food Chem 48: 1243-1246
- Lyons MM, Yu C, Toma RB (2003) Resveratrol in raw and baked blueberries and bilberries. J Agric Food Chem 51: 5867-5870.
- Vastano BC, Chen Y, Zhu N (2000) Isolation and identification of stilbenes in two varieties of Polygonum cuspidatum. J Agric Food Chem 48: 253-256
- Jang M, Cai L, Udeani GO (1997) Cancer chemopreventive activity of resveratrol, a natural product derived from grapes. Science 275: 218-220
- Hung LM, Chen JK, Huang SS (2000) Cardioprotective effect of resveratrol, a natural antioxidant derived from grapes. Cardiovasc Res 47: 549-555.
- Baur JA, Pearson KJ, Price NL (2006) Resveratrol improves health and survival of mice on a high-calorie diet. Nature 444: 337-342
- Kang L, Heng W, Yuan A (2010) Resveratrol modulates adipokine expression and improves insulin sensitivity in adipocytes: Relative to inhibition of inflammatory responses. Biochimie 92: 789-796.
- Afaq F, Adhami VM, Ahmad N (2003) Prevention of short-term ultraviolet B radiation-mediated damages by resveratrol in SKH-1 hairless mice. Toxicol Appl Pharmacol 186: 28-37.
- Reagan S, Afaq F, Aziz MH, Ahmad N (2004) Modulations of critical cell cycle regulatory events during chemoprevention of ultraviolet B-mediated responses by resveratrol in SKH-1 hairless mouse skin. Oncogene 23: 5151-5160
- Murakami A, Matsumoto K, Koshimizu K, Ohigashi H (2003) Effects of selected food factors with chemopreventive properties on combined lipopolysaccharide- and interferon-gamma-induced IkappaB degradation in RAW264.7 macrophages. Cancer Lett 195: 17-25
- Lopez JM, Garcia CF (2008) Aggregation state and pKa values of (E) -resveratrol as determined by fluorescence spectroscopy and UV-visible absorption. J Agric Food Chem 56: 7600-7605.
- Mendes JB, Riekes MK, de Oliveira VM (2012) PHBV/PCL microparticles for controlled release of resveratrol: physicochemical characterization, antioxidant potential, and effect on hemolysis of human erythrocytes. Scientific World Journal 2012: 1-13.
- Laza AL, Gref R, Couvreur P (2010) Cyclodextrins for drug delivery. J Drug Target 18: 645-656
- Kobierski S, Ofori K, Muller RH, Keck CM (2009) Resveratrol nanosuspensions for dermal application-production, characterization, and physical stability. Pharmazie 64: 741-747.
- Figueiro F, Bernardi A, Frozza RL (2013) Resveratrol-loaded lipid-core nanocapsules treatment reduces in vitro and in vivo glioma growth. J Biomed Nanotechnol 9: 516-526.
- Szabo G (2009) A glass of red wine to improve mitochondrial biogenesis? Novel mechanisms of resveratrol. Am J Physiol Heart Circ Physiol 297: 8-9
- Agarwal A, Prabakaran SA (2005) Mechanism, measurement, and prevention of oxidative stress in male reproductive physiology. Indian J Exp Biol 43: 963-974.
- Fukao H, Ijiri Y, Miura M (2004) Effect of trans-resveratrol on the thrombogenicity and atherogenicity in apolipoprotein E-deficient and low-density lipoprotein receptor-deficient mice. Blood Coagul Fibrinolysis 15: 441-446
- Wallerath T, Deckert G, Ternes T (2002) Resveratrol, a polyphenolic phytoalexin present in red wine, enhances expression and activity of endothelial nitric oxide synthase. Circulation 106: 1652-1658.
- Elmadhun NY, Sabe AA, Robich MP (2013) The pig as a valuable model for testing the effect of resveratrol to prevent cardiovascular disease. Ann N Y Acad Sci 1290: 130-135.
- Sahu SS, Madhyastha S, Rao GM (2013) Neuroprotective effect of resveratrol against prenatal stress induced cognitive impairment and possible involvement of Na (+) , K (+) -ATPase activity. Pharmacol Biochem Behav 103: 520-525
- Palsamy P, Subramanian S (2008) Resveratrol, a natural phytoalexin, normalizes hyperglycemia in streptozotocin-nicotinamide induced experimental diabetic rats. Biomed Pharmacother 62: 598-605.
- Sebastia N, Almonacid M, Villaescusa JI (2013) Radioprotective activity and cytogenetic effect of resveratrol in human lymphocytes: an in vitro evaluation. Food Chem Toxicol 51: 391-395.
- Baek SH, Ko JH, Lee H (2016) Resveratrol inhibits STAT3 signaling pathway through the induction of SOCS-1: Role in apoptosis induction and radiosensitization in head and neck tumor cells. Phytomedicine 23: 566-577
- Parfenov M, Pedamallu CS, Gehlenborg N (2014) Characterization of HPV and host genome interactions in primary head and neck cancers. Proc Natl Acad Sci U S A 111: 15544-15549.
- Masuelli L, Di Stefano E, Fantini M (2014) Resveratrol potentiates the in vitro and in vivo anti-tumoral effects of curcumin in head and neck carcinomas. Oncotarget 5: 10745-10762.
- Cai Y, Zhao L, Qin Y (2015) Resveratrol inhibits proliferation and induces apoptosis of nasopharyngeal carcinoma cell line C666-1 through AMPK activation. Pharmazie 70: 399-403.
- Zhang M, Zhou X, Zhou K (2013) Resveratrol inhibits human nasopharyngeal carcinoma cell growth via blocking pAkt/p70S6K signaling pathways. Int J Mol Med 31: 621-627.
- Chow SE, Wang JS, Chuang SF (2010) Resveratrol-induced p53-independent apoptosis of human nasopharyngeal carcinoma cells is correlated with the downregulation of DeltaNp63. Cancer Gene Ther 17: 872-882.
- Mikami S, Ota I, Masui T (2016) Effect of resveratrol on cancer progression through the REG expression pathway in head and neck cancer cells. Int J Oncol 49: 1553-1560
- Feng Y, Yang Y, Fan C (2016) Pterostilbene Inhibits the Growth of Human Esophageal Cancer Cells by Regulating Endoplasmic Reticulum Stress. Cell Physiol Biochem 38: 1226-1244.
- Yu XD, Yang JL, Zhang WL (2016) Resveratrol inhibits oral squamous cell carcinoma through induction of apoptosis and G2/M phase cell cycle arrest. Tumour Biol 37: 2871-2877
- Lin FY, Hsieh YH, Yang SF (2015) Resveratrol suppresses TPA-induced matrix metalloproteinase-9 expression through the inhibition of MAPK pathways in oral cancer cells. J Oral Pathol Med 44: 699-706.
- Atienzar AN, Camacho F, Lopez P (2014) Effects of resveratrol and irradiation upon oral squamous cell carcinoma cells. Acta Odontol Scand 72: 481-488.
- Shan Z, Yang G, Xiang W (2014) Effects of resveratrol on oral squamous cell carcinoma (OSCC) cells in vitro. J Cancer Res Clin Oncol 140: 371-374
- Chow SE, Kao CH, Liu YT (2014) Resveratrol induced ER expansion and ER caspase-mediated apoptosis in human nasopharyngeal carcinoma cells. Apoptosis 19: 527-541
- Shrotriya S, Tyagi A, Deep G (2015) Grape seed extract and resveratrol prevent 4-nitroquinoline 1-oxide induced oral tumorigenesis in mice by modulating AMPK activation and associated biological responses. Mol Carcinog 54: 291-300.
- Yu XM, Jaskula R, Ahmed K (2013) Resveratrol induces differentiation markers expression in anaplastic thyroid carcinoma via activation of Notch1 signaling and suppresses cell growth. Mol Cancer Ther 12: 1276-1287.
- Hu FW, Tsai LL (2012) Impairment of tumor-initiating stem-like property and reversal of epithelial-mesenchymal transdifferentiation in head and neck cancer by resveratrol treatment. Mol Nutr Food Res 56: 1247-1258.
- Tyagi A, Gu M, Takahata T (2011) Resveratrol selectively induces DNA Damage, independent of Smad4 expression, in its efficacy against human head and neck squamous cell carcinoma. Clin Cancer Res 17: 5402-5411.
- Truong M, Cook MR, Pinchot SN (2011) Resveratrol induces Notch2-mediated apoptosis and suppression of neuroendocrine markers in medullary thyroid cancer. Ann Surg Oncol 18: 1506-1511.
- Huang TT, Lin HC, Chen CC (2011) Resveratrol induces apoptosis of human nasopharyngeal carcinoma cells via activation of multiple apoptotic pathways. J Cell Physiol 226: 720-728.
- Lin HY, Sun M, Tang HY (2008) Resveratrol causes COX-2- and p53-dependent apoptosis in head and neck squamous cell cancer cells. J Cell Biochem 104: 2131-2142.
- Shih A, Davis FB, Lin HY, Davis PJ (2002) Resveratrol induces apoptosis in thyroid cancer cell lines via a MAPK- and p53-dependent mechanism. J Clin Endocrinol Metab 87: 1223-1232
- Lin Y, Yngve A, Lagergren J , Lu Y (2014) A dietary pattern rich in lignans, quercetin and resveratrol decreases the risk of oesophageal cancer. Br J Nutr 112: 2002-2009.
- Tang Q, Li G, Wei X (2013) Resveratrol-induced apoptosis is enhanced by inhibition of autophagy in esophageal squamous cell carcinoma. Cancer Lett 336: 325-337
- Li ZG, Hong T, Shimada Y (2002) Suppression of N-nitroso methyl benzylamine (NMBA) -induced esophageal tumorigenesis in F344 rats by resveratrol. Carcinogenesis 23: 1531-1536.
- Zhou HB, Yan Y, Sun YN, Zhu J (2003) Resveratrol induces apoptosis in human esophageal carcinoma cells. World J Gastroenterol 9: 408-411
- Fan GH, Wang ZM, Yang X (2014) Resveratrol inhibits oesophageal adenocarcinoma cell proliferation via AMP-activated protein kinase signaling. Asian Pac J Cancer Prev 15: 677-682.
- Woodall CE, Li Y, Liu QH, Wo J (2009) Chemoprevention of metaplasia initiation and carcinogenic progression to esophageal adenocarcinoma by resveratrol supplementation. Anticancer Drugs 20: 437-443.
- Szumilo J (2009) Natural compounds in chemoprevention of esophageal squamous cell tumors experimental studies. Pol Merkur Lekarski 26: 156-161.
- Jemal A, Bray F, Center MM (2011) Global cancer statistics. CA Cancer J Clin 61: 69-90.
- Bertuccio P, Chatenoud L, Levi F (2009) Recent patterns in gastric cancer: a global overview. Int J Cancer 125: 666-673.
- Zaidi SF, Ahmed K, Yamamoto T (2009) Effect of resveratrol on Helicobacter pylori-induced interleukin-8 secretion, reactive oxygen species generation and morphological changes in human gastric epithelial cells. Biol Pharm Bull 32: 1931-1935
- Yang Q, Wang B, Zang W (2013) Resveratrol inhibits the growth of gastric cancer by inducing G1 phase arrest and senescence in a Sirt1-dependent manner. PLoS One 8: 1-9.
- Zhou HB, Chen JJ, Wang WX (2005) Anticancer activity of resveratrol on implanted human primary gastric carcinoma cells in nude mice. World J Gastroenterol 11: 280-284.
- Xu J, Liu D, Niu H (2017) Resveratrol reverses Doxorubicin resistance by inhibiting epithelial-mesenchymal transition (EMT) through modulating PTEN/Akt signaling pathway in gastric cancer. J Exp Clin Cancer Res 36: 19.
- Jing X, Cheng W, Wang S, Li P (2016) Resveratrol induces cell cycle arrest in human gastric cancer MGC803 cells via the PTEN-regulated PI3K/Akt signaling pathway. Oncol Rep 35: 472-478
- Gao Q, Yuan Y, Gan HZ, Peng Q (2015) Resveratrol inhibits the hedgehog signaling pathway and epithelial-mesenchymal transition and suppresses gastric cancer invasion and metastasis. Oncol Lett 9: 2381-2387.
- Liu ML, Zhang SJ (2014) Effects of resveratrol on the protein expression of survivin and cell apoptosis in human gastric cancer cells. J BUON 19: 713-717
- Shin KO, Park NY, Seo CH (2012) Inhibition of sphingolipid metabolism enhances resveratrol chemotherapy in human gastric cancer cells. Biomol Ther (Seoul) 20: 470-476.
- Wang Z, Li W, Meng X, Jia B (2012) Resveratrol induces gastric cancer cell apoptosis via reactive oxygen species, but independent of sirtuin1. Clin Exp Pharmacol Physiol 39: 227-232.
- Mitrut P, Burada F, Enescu A (2009) The genotoxicity study of resveratrol in primary gastric adenocarcinoma cell cultures. Rom J Morphol Embryol 50: 429-433.
- Signorelli P, Munoz JM (2009) Dihydroceramide intracellular increase in response to resveratrol treatment mediates autophagy in gastric cancer cells. Cancer Lett 282: 238-243.
- Aquilano K, Baldelli S, Rotilio G, Ciriolo MR (2009) trans-Resveratrol inhibits H2O2-induced adenocarcinoma gastric cells proliferation via inactivation of MEK1/2-ERK1/2-c-Jun signalling axis. Biochem Pharmacol 77: 337-347
- Zheng GH, Li HQ (2008) Effects of garlic oil combined with resveratrol on inducting of apoptosis and expression of Fas, bcl-2 and bax in human gastric cancer cell line Chi Jour of Preven Med 42: 39-42.
- Riles WL, Erickson J, Nayyar S (2006) Resveratrol engages selective apoptotic signals in gastric adenocarcinoma cells. World J Gastroenterol 12: 5628-5634.
- Atten MJ, Godoy RE, Attar BM (2005) Resveratrol regulates cellular PKC alpha and delta to inhibit growth and induce apoptosis in gastric cancer cells. Invest New Drugs 23: 111-119.
- Holian O, Wahid S, Atten MJ (2002) Inhibition of gastric cancer cell proliferation by resveratrol: role of nitric oxide. Am J Physiol Gastrointest Liver Physiol 282: 809-816.
- Atten MJ, Attar BM, Milson T, Holian O (2001) Resveratrol-induced inactivation of human gastric adenocarcinoma cells through a protein kinase C-mediated mechanism. Biochem Pharmacol 62: 1423-1432.
- Siegel R, Naishadham D, Jemal A (2012) Cancer statistics. Cancer J Clin 62: 10-29
- Willett WC (1995) Diet, nutrition, and avoidable cancer. Environ Health Perspect 103 Suppl 8: 165-170.
- Buhrmann C, Shayan P, Kraehe P (2015) Resveratrol induces chemosensitization to 5-fluorouracil through up-regulation of intercellular junctions, Epithelial-to-mesenchymal transition and apoptosis in colorectal cancer. Biochem Pharmacol 98: 51-68.
- Jeong JB, Lee J, Lee SH (2015) TCF4 Is a Molecular Target of Resveratrol in the Prevention of Colorectal Cancer. Int J Mol Sci 16: 10411-10425.
- Ji Q, Liu X, Fu X (2013) Resveratrol inhibits invasion and metastasis of colorectal cancer cells via MALAT1 mediated Wnt/beta-catenin signal pathway. PLoS One 8: 78700.
- Park JW, Woo KJ, Lee JT (2007) Resveratrol induces pro-apoptotic endoplasmic reticulum stress in human colon cancer cells. Oncol Rep 18: 1269-1273
- Wolter F, Akoglu B, Clausnitzer A, Stein J (2001) Downregulation of the cyclin D1/Cdk4 complex occurs during resveratrol-induced cell cycle arrest in colon cancer cell lines. J Nutr 131: 2197-2203.
- Buhrmann C, Shayan P, Popper B, Goel A (2016) Sirt1 Is Required for Resveratrol-Mediated Chemopreventive Effects in Colorectal Cancer Cells. Nutrients 8: 145.
- Karimi DF, Saidijam M (2016) Resveratrol Inhibits Proliferation, Invasion, and Epithelial-Mesenchymal Transition by Increasing miR-200c Expression in HCT-116 Colorectal Cancer Cells. J Cell Biochem 118: 1547-1555.
- Du Z, Zhou F, Jia Z (2016) The hedgehog/Gli-1 signaling pathways is involved in the inhibitory effect of resveratrol on human colorectal cancer HCT116 cells. Iran J Basic Med Sci 19: 1171-1176.
- Feng M, Zhong LX (2016) Resveratrol Treatment Inhibits Proliferation of and Induces Apoptosis in Human Colon Cancer Cells. Med Sci Monit 22: 1101-1108.
- Yang S, Li W, Sun H (2015) Resveratrol elicits anti-colorectal cancer effect by activating miR-34c-KITLG in vitro and in vivo. BMC Cancer 15: 1-11
- Yuan SX, Wang DX, Wu QX (2016) BMP9/p38 MAPK is essential for the antiproliferative effect of resveratrol on human colon cancer. Oncol Rep 35: 939-947.
- Cai H, Scott E, Kholghi A (2015) Cancer chemoprevention: Evidence of a nonlinear dose response for the protective effects of resveratrol in humans and mice. Sci Transl Med 7: 298ra117.
- Yang J, Liu J, Lyu X, Fei S (2015) Resveratrol inhibits cell proliferation and up-regulates MICA/B expression in human colon cancer stem cells. 31: 889-893.
- Demoulin B, Hermant M, Castrogiovanni C (2015) Resveratrol induces DNA damage in colon cancer cells by poisoning topoisomerase II and activates the ATM kinase to trigger p53-dependent apoptosis. Toxicol In Vitro 29: 1156-1165
- Patel KR, Brown VA, Jones DJ (2010) Clinical pharmacology of resveratrol and its metabolites in colorectal cancer patients. Cancer Res 70: 7392-7399.
- Nguyen AV, Martinez M, Stamos MJ (2009) Results of a phase I pilot clinical trial examining the effect of plant-derived resveratrol and grape powder on Wnt pathway target gene expression in colonic mucosa and colon cancer. Cancer Manag Res 1: 25-37.
- Howells LM, Berry DP, Elliott PJ (2011) Phase I randomized, double-blind pilot study of micronized resveratrol (SRT501) in patients with hepatic metastases--safety, pharmacokinetics, and pharmacodynamics. Cancer Prev Res (Phila) 4: 1419-1425
- Ji Q, Liu X, Han Z (2015) Resveratrol suppresses epithelial-to-mesenchymal transition in colorectal cancer through TGF-beta1/Smads signaling pathway mediated Snail/E-cadherin expression. BMC Cancer 15: 1-12
- Saud SM, Li W, Morris NL (2014) Resveratrol prevents tumorigenesis in mouse model of Kras activated sporadic colorectal cancer by suppressing oncogenic Kras expression. Carcinogenesis 35: 2778-2786.
- Ali I, Braun DP (2014) Resveratrol enhances mitomycin C-mediated suppression of human colorectal cancer cell proliferation by up-regulation of p21WAF1/CIP1. Anticancer Res 34: 5439-5446.
- Liu B, Zhou Z, Zhou W (2014) Resveratrol inhibits proliferation in human colorectal carcinoma cells by inducing G1/Sphase cell cycle arrest and apoptosis through caspase/cyclinCDK pathways. Mol Med Rep 10: 1697-1702.
- Liu YZ, Wu K, Huang J (2014) The PTEN/PI3K/Akt and Wnt/beta-catenin signaling pathways are involved in the inhibitory effect of resveratrol on human colon cancer cell proliferation. Int J Oncol 45: 104-112.
- Fouad MA, Agha AM, Merzabani MM, Shouman SA (2013) Resveratrol inhibits proliferation, angiogenesis and induces apoptosis in colon cancer cells: calorie restriction is the force to the cytotoxicity. Hum Exp Toxicol 32: 1067-1080
- Miki H, Uehara N, Kimura A (2012) Resveratrol induces apoptosis via ROS-triggered autophagy in human colon cancer cells. Int J Oncol 40: 1020-1028.
- Radhakrishnan S, Reddivari L, Sclafani R, Das UN (2011) Resveratrol potentiates grape seed extract induced human colon cancer cell apoptosis. Front Biosci (Elite Ed) 3: 1509-1523.
- Vanamala J, Reddivari L, Radhakrishnan S, Tarver C (2010) Resveratrol suppresses IGF-1 induced human colon cancer cell proliferation and elevates apoptosis via suppression of IGF-1R/Wnt and activation of p53 signaling pathways. BMC Cancer 10: 238.
- Cosan D, Soyocak A, Basaran A (2009) The effects of resveratrol and tannic acid on apoptosis in colon adenocarcinoma cell line. Saudi Med J 30: 191-195.
- Juan ME, Wenzel U, Daniel H, Planas JM (2008) Resveratrol induces apoptosis through ROS- dependent mitochondria pathway in HT-29 human colorectal carcinoma cells. J Agric Food Chem 56: 4813-4818.
- Fuggetta MP, Lanzilli G, Tricarico M (2006) Effect of resveratrol on proliferation and telomerase activity of human colon cancer cells in vitro. J Exp Clin Cancer Res 25: 189-193.
- Mohan J, Gandhi AA, Bhavya BC (2006) Caspase-2 triggers Bax-Bak-dependent and -independent cell death in colon cancer cells treated with resveratrol. J Biol Chem 281: 17599-17611.
- Mahyar RM, Kohler H and Roemer K (2002) Role of Bax in resveratrol-induced apoptosis of colorectal carcinoma cells. BMC Cancer 2: 27
- Delmas D, Passilly DP (2002) Resveratrol, a chemopreventive agent, disrupts the cell cycle control of human SW480 colorectal tumor cells. Int J Mol Med 10: 193-199.
- Ferlay J, Soerjomataram I, Dikshit R (2015) Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer 136: 359-386.
- Yu MC, Yuan JM (2004) Environmental factors and risk for hepatocellular carcinoma. Gastroenterology 127: 72-78.
- Parekh P, Motiwale L, Naik N, Rao KV (2001) Downregulation of cyclin D1 is associated with decreased levels of p38 MAP kinases, Akt/PKB and Pak1 during chemopreventive effects of resveratrol in liver cancer cells. Exp Toxicol Pathol 63: 167-173.
- Yu L, Sun ZJ, Wu SL, Pan CE (2003) Effect of resveratrol on cell cycle proteins in murine transplantable liver cancer. World J Gastroenterol 9: 2341-2343.
- Wu SL, Sun ZJ, Yu L, Meng KW, Qin XL (2004) Effect of resveratrol and in combination with 5-FU on murine liver cancer. World J Gastroenterol 10: 3048-3052.
- Li Y, Zhu W, Li J, Liu M, Wei M, et al. (2013) Resveratrol suppresses the STAT3 signaling pathway and inhibits proliferation of high glucose-exposed HepG2 cells partly through SIRT1. Oncol Rep 30: 2820-2828.
- Zhang H, Yang R (2014) Resveratrol inhibits VEGF gene expression and proliferation of hepato carcinoma cells. Hepato gastro enterology 61: 410-412.
- Wang G, Guo X, Chen H (2012) A resveratrol analog, phoyunbene B, induces G2/M cell cycle arrest and apoptosis in HepG2 liver cancer cells. Bioorg Med Chem Lett 22: 2114-2118.
- Du Q, Hu B, An HM (2013) Synergistic anticancer effects of curcumin and resveratrol in Hepa1-6 hepatocellular carcinoma cells. Oncol Rep 29: 1851-1858.
- Zhang XL, Yu H, Xiong YY (2013) Resveratrol down-regulates Myosin light chain kinase, induces apoptosis and inhibits diethylnitrosamine-induced liver tumorigenesis in rats. Int J Mol Sci 14: 1940-1951.
- Yeh CB, Hsieh MJ, Lin CW (2013) The antimetastatic effects of resveratrol on hepatocellular carcinoma through the downregulation of a metastasis-associated protease by SP-1 modulation. PLoS One 8: e56661.
- Villa E, Boylan JM, Tatar M, Gruppuso PA (2011) Resveratrol inhibits protein translation in hepatic cells. PLoS One 6: e29513
- Xie Q, Yang Y, Wang Z, Chen F (2014) Resveratrol-4-O-D- (2'-galloyl) -glucopyranoside isolated from Polygonum cuspidatum exhibits anti-hepatocellular carcinoma viability by inducing apoptosis via the JNK and ERK pathway. Molecules 19: 1592-1602.
- Rajasekaran D, Elavarasan J, Sivalingam M (2011) Resveratrol interferes with N-nitrosodiethylamine-induced hepatocellular carcinoma at early and advanced stages in male Wistar rats. Mol Med Rep 4: 1211-1217.
- Weng CJ, Wu CF, Huang HW (2010) Evaluation of anti-invasion effect of resveratrol and related methoxy analogues on human hepatocarcinoma cells. J Agric Food Chem 58: 2886-2894.
- Bishayee A, Dhir N (2009) Resveratrol-mediated chemoprevention of diethylnitrosamine-initiated hepatocarcinogenesis: inhibition of cell proliferation and induction of apoptosis. Chem Biol Interact 179: 131-144
- Bishayee A, Waghray A, Barnes KF (2010) Suppression of the inflammatory cascade is implicated in resveratrol chemoprevention of experimental hepatocarcinogenesis. Pharm Res 27: 1080-1091.
- Yu HB, Zhang HF, Zhang X (2010) Resveratrol inhibits VEGF expression of human hepatocellular carcinoma cells through a NF-kappa B-mediated mechanism. Hepatogastroenterology 57: 1241-1246.
- Liao PC, Ng LT, Lin LT (2010) Resveratrol arrests cell cycle and induces apoptosis in human hepatocellular carcinoma Huh-7 cells. J Med Food 13: 1415-1423.
- Kuo PL, Chiang LC, Lin CC (2002) Resveratrol- induced apoptosis is mediated by p53-dependent pathway in Hep G2 cells. Life Sci 72: 23-34.
- Delmas D, Jannin B (2000) Inhibitory effect of resveratrol on the proliferation of human and rat hepatic derived cell lines. Oncol Rep 7: 847-852.
- Sun ZJ, Pan CE, Liu HS (2002) Anti-hepatoma activity of resveratrol in vitro. World J Gastroenterol 8: 79-81
- Yu H, Pan C, Zhao S (2008) Resveratrol inhibits tumor necrosis factor-alpha-mediated matrix metalloproteinase-9 expression and invasion of human hepatocellular carcinoma cells. Biomed Pharmacother 62: 366-372
- Miura D, Miura Y, Yagasaki K (2003) Hypolipidemic action of dietary resveratrol, a phytoalexin in grapes and red wine, in hepatoma-bearing rats. Life Sci 73: 1393-1400.
- Kozuki Y, Miura Y, Yagasaki K (2001) Resveratrol suppresses hepatoma cell invasion independently of its anti-proliferative action. Cancer Lett 167: 151-156.
- Notas G, Nifli AP, Kampa M (2006) Resveratrol exerts its antiproliferative effect on HepG2 hepatocellular carcinoma cells, by inducing cell cycle arrest, and NOS activation. Biochim Biophys Acta 1760: 1657-1666.
- Guo L, Tan K, Wang H, Zhang X (2016) Pterostilbene inhibits hepatocellular carcinoma through p53/SOD2/ROS-mediated mitochondrial apoptosis. Oncol Rep 36: 3233-3240.
- De LV, Monvoisin A, Neaud V (2001) Trans-resveratrol, a grapevine-derived polyphenol, blocks hepatocyte growth factor-induced invasion of hepatocellular carcinoma cells. Int J Oncol 19: 83-88.
- Gao F, Deng G, Liu W, Zhou K, Li M, et al. (2017) Resveratrol suppresses human hepatocellular carcinoma via targeting HGF-c-Met signaling pathway. Oncol Rep 37: 1203-1211.
- Schaid DJ (2004) The complex genetic epidemiology of prostate cancer. Hum Mol Genet 13 Spec No 1: R103-121.
- Sheth S, Jajoo S, Kaur T (2012) Resveratrol reduces prostate cancer growth and metastasis by inhibiting the Akt/MicroRNA-21 pathway. PLoS One 7: e51655.
- Li J, Chong T, Wang Z (2014) A novel anticancer effect of resveratrol: reversal of epithelialmesenchymal transition in prostate cancer cells. Mol Med Rep 10: 1717-1724.
- Mitani T, Harada N, Tanimori S (2014) Resveratrol inhibits hypoxia-inducible factor-1alpha-mediated androgen receptor signaling and represses tumor progression in castration-resistant prostate cancer. J Nutr Sci Vitaminol (Tokyo) 60: 276-282.
- Ganapathy S, Chen Q, Singh KP, Shankar S (2010) Resveratrol enhances antitumor activity of TRAIL in prostate cancer xenografts through activation of FOXO transcription factor. PLoS One 5: e15627.
- Benitez DA, Hermoso MA (2009) Regulation of cell survival by resveratrol involves inhibition of NF kappa B-regulated gene expression in prostate cancer cells. Prostate 69: 1045-1054
- Singh SK, Banerjee S, Acosta EP (2017) Resveratrol induces cell cycle arrest and apoptosis with docetaxel in prostate cancer cells via a p53/ p21WAF1/CIP1 and p27KIP1 pathway. Oncotarget 8: 17216-17228.
- Kumar S, Eroglu E, Stokes JA (2017) Resveratrol induces mitochondria-mediated, caspase-independent apoptosis in murine prostate cancer cells. Oncotarget 8: 20895-20908.
- Taniguchi T, Iizumi Y, Watanabe M (2016) Resveratrol directly targets DDX5 resulting in suppression of the mTORC1 pathway in prostate cancer. Cell Death Dis 7: e2211.
- Selvaraj S, Sun Y, Sukumaran P, Singh BB (2016) Resveratrol activates autophagic cell death in prostate cancer cells via downregulation of STIM1 and the mTOR pathway. Mol Carcinog 55: 818-831.
- Dhar S, Kumar A, Li K, Tzivion G, Levenson AS, et al. (2015) Resveratrol regulates PTEN/Akt pathway through inhibition of MTA1/HDAC unit of the NuRD complex in prostate cancer. Biochim Biophys Acta 1853: 265-275.
- Lee MH, Kundu JK, Keum YS (2014) Resveratrol Inhibits IL-6-Induced Transcriptional Activity of AR and STAT3 in Human Prostate Cancer LNCaP-FGC Cells. Biomol Ther (Seoul) 22: 426-430.
- Ferruelo A, Romero I, Cabrera PM (2014) Effects of resveratrol and other wine polyphenols on the proliferation, apoptosis and androgen receptor expression in LNCaP cells. Actas Urol Esp 38: 397-404.
- Fang Y, Bradley MJ, Cook KM (2013) A potential role for resveratrol as a radiation sensitizer for melanoma treatment. J Surg Res 183: 645-653.
- Khan MA, Chen HC, Wan XX (2013) Regulatory effects of resveratrol on antioxidant enzymes: a mechanism of growth inhibition and apoptosis induction in cancer cells. Mol Cells 35: 219-225.
- Osmond GW, Masko EM, Tyler D (2013) In vitro and in vivo evaluation of resveratrol and 3,5-dihydroxy-4'-acetoxy-trans-stilbene in the treatment of human prostate carcinoma and melanoma. J Surg Res 179: 141-148
- Fang Y, DeMarco VG, Nicholl MB (2012) Resveratrol enhances radiation sensitivity in prostate cancer by inhibiting cell proliferation and promoting cell senescence and apoptosis. Cancer Sci 103: 1090-1098.
- Rashid A, Liu C, Sanli T (2011) Resveratrol enhances prostate cancer cell response to ionizing radiation. Modulation of the AMPK, Akt and mTOR pathways. Radiat Oncol 6: 144
- Harada N, Atarashi K, Murata Y (2011) Inhibitory mechanisms of the transcriptional activity of androgen receptor by resveratrol: Implication of DNA binding and acetylation of the receptor. J Steroid Biochem Mol Biol 123: 65-70.
- Chakraborty A, Gupta N, Ghosh K, Roy P (2010) In vitro evaluation of the cytotoxic, anti-proliferative and anti-oxidant properties of pterostilbene isolated from Pterocarpus marsupium. Toxicol In Vitro 24: 1215-1228.
- Wang TT, Schoene NW (2010) Differential effects of resveratrol and its naturally occurring methylether analogs on cell cycle and apoptosis in human androgen-responsive LNCaP cancer cells. Mol Nutr Food Res 54: 335-344.
- Shi WF, Leong M, Cho E (2009) Repressive effects of resveratrol on androgen receptor transcriptional activity. PLoS One 4: e7398
- Kai L, Samuel SK, Levenson AS (2010) Resveratrol enhances p53 acetylation and apoptosis in prostate cancer by inhibiting MTA1/NuRD complex. Int J Cancer 126: 1538-1548
- Hsieh TC (2009) Antiproliferative effects of resveratrol and the mediating role of resveratrol targeting protein NQO2 in androgen receptor-positive, hormone-non-responsive CWR22Rv1 cells. Anticancer Res 29: 3011-3017.
- Gill C, Walsh SE, Morrissey C (2007) Resveratrol sensitizes androgen independent prostate cancer cells to death-receptor mediated apoptosis through multiple mechanisms. Prostate 67: 1641-1653.
- Shankar S, Chen Q, Siddiqui I (2007) Sensitization of TRAIL-resistant LNCaP cells by resveratrol (3, 4', 5 tri-hydroxystilbene) : molecular mechanisms and therapeutic potential. J Mol Signal 2: 7
- Harper CE, Patel BB, Wang J (2007) Resveratrol suppresses prostate cancer progression in transgenic mice. Carcinogenesis 28: 1946-1953
- Benitez DA, Pozo GE, Clementi M (2007) Non-genomic action of resveratrol on androgen and oestrogen receptors in prostate cancer: modulation of the phosphoinositide 3-kinase pathway. Br J Cancer 96: 1595-1604.
- Scarlatti F, Sala G, Ricci C (2007) Resveratrol sensitization of DU145 prostate cancer cells to ionizing radiation is associated to ceramide increase. Cancer Lett 253: 124-130.
- Aziz MH, Nihal M, Fu VX (2006) Resveratrol-caused apoptosis of human prostate carcinoma LNCaP cells is mediated via modulation of phosphatidylinositol 3'-kinase/Akt pathway and Bcl-2 family proteins. Mol Cancer Ther 5: 1335-1341.
- Scifo C, Cardile V, Russo A (2004) Resveratrol and propolis as necrosis or apoptosis inducers in human prostate carcinoma cells. Oncol Res 14: 415-426.
- Gao S, Liu GZ, Wang Z (2004) Modulation of androgen receptor-dependent transcription by resveratrol and genistein in prostate cancer cells. Prostate 59: 214-225.
- Cardile V, Scifo C, Russo A (2003) Involvement of HSP70 in resveratrol-induced apoptosis of human prostate cancer. Anticancer Res 23: 4921-4926.
- Kim YA, Rhee SH, Park KY (2003) Antiproliferative effect of resveratrol in human prostate carcinoma cells. J Med Food 6: 273-280.
- Narayanan BA, Narayanan NK (2003) Differential expression of genes induced by resveratrol in LNCaP cells: P53-mediated molecular targets. Int J Cancer 104: 204-212.
- Ding XZ, Adrian TE (2002) Resveratrol inhibits proliferation and induces apoptosis in human pancreatic cancer cells. Pancreas 25: 71-76
- Morris GZ, Williams RL, Elliott MS, Beebe SJ (2002) Resveratrol induces apoptosis in LNCaP cells and requires hydroxyl groups to decrease viability in LNCaP and DU 145 cells. Prostate 52: 319-329
- Kuwajerwala N, Cifuentes E (2002) Resveratrol induces prostate cancer cell entry into s phase and inhibits DNA synthesis. Cancer Res 62: 2488-2492.
- Mitchell SH, Zhu W, Young CY (1999) Resveratrol inhibits the expression and function of the androgen receptor in LNCaP prostate cancer cells. Cancer Res 59: 5892-5895.
- Hsieh TC, Wu JM (1999) Differential effects on growth, cell cycle arrest, and induction of apoptosis by resveratrol in human prostate cancer cell lines. Exp Cell Res 249: 109-115.
- Kamisawa T, Wood LD, Itoi T,Takaori K (2016) Pancreatic cancer. Lancet 388: 73-85.
- Li W, Cao L, Chen X, Lei J (2016) Resveratrol inhibits hypoxia-driven ROS-induced invasive and migratory ability of pancreatic cancer cells via suppression of the Hedgehog signaling pathway. Oncol Rep 35: 1718-1726
- Zhou JH, Cheng HY (2011) Resveratrol induces apoptosis in pancreatic cancer cells. Chin Med J (Engl) 124: 1695-1699.
- Li W, Ma J, Ma Q (2013) Resveratrol inhibits the epithelial-mesenchymal transition of pancreatic cancer cells via suppression of the PI-3K/Akt/NF-kappaB pathway. Curr Med Chem 20: 4185-4194.
- Cui J, Sun R, Yu Y (2010) Antiproliferative effect of resveratrol in pancreatic cancer cells. Phytother Res 24: 1637-1644
- Shankar S, Nall D, Tang SN (2011) Resveratrol inhibits pancreatic cancer stem cell characteristics in human and KrasG12D transgenic mice by inhibiting pluripotency maintaining factors and epithelial-mesenchymal transition. PLoS One 6: e16530
- Cao L, Chen X, Xiao X (2016) Resveratrol inhibits hyperglycemia-driven ROS-induced invasion and migration of pancreatic cancer cells via suppression of the ERK and p38 MAPK signaling pathways. Int J Oncol 49: 735-743.
- Mannal PW, Alosi JA, Schneider JG (2010) Pterostilbene inhibits pancreatic cancer in vitro. J Gastrointest Surg 14: 873-879.
- Zhu M, Zhang Q, Wang X (2016) Metformin potentiates anti-tumor effect of resveratrol on pancreatic cancer by down-regulation of VEGF-B signaling pathway. Oncotarget 7: 84190-84200
- Jiang Z, Chen X, Chen K (2016) YAP Inhibition by Resveratrol via Activation of AMPK Enhances the Sensitivity of Pancreatic Cancer Cells to Gemcitabine. Nutrients 8: 1-14.
- Kato A, Naiki A, Nakazawa T (2015) Chemopreventive effect of resveratrol and apocynin on pancreatic carcinogenesis via modulation of nuclear phosphorylated GSK3beta and ERK1/2. Oncotarget 6: 42963-42975
- Qin Y, Ma Z, Dang X, Li W, Ma Q (2014) Effect of resveratrol on proliferation and apoptosis of human pancreatic cancer MIA PaCa-2 cells may involve inhibition of the Hedgehog signaling pathway. Mol Med Rep 10: 2563-2567.
- Yang L, Yang L, Tian W (2014) Resveratrol plays dual roles in pancreatic cancer cells. J Cancer Res Clin Oncol 140: 749-755
- Liu P, Liang H, Xia Q (2013) Resveratrol induces apoptosis of pancreatic cancers cells by inhibiting miR-21 regulation of BCL-2 expression. Clin Transl Oncol 15: 741-746.
- Mo W, Xu X, Xu L (2011) Resveratrol inhibits proliferation and induces apoptosis through the hedgehog signaling pathway in pancreatic cancer cell. Pancreatology 11: 601-609.
- Roy SK, Chen Q, Fu J, Shankar S, Srivastava RK (2011) Resveratrol inhibits growth of orthotopic pancreatic tumors through activation of FOXO transcription factors. PLoS One 6: e25166.
- Bortolotti C, Kunit T, Moder A (2009) The phytostilbene resveratrol induces apoptosis in INS-1E rat insulinoma cells. Cell Physiol Biochem 23: 245-254.
- Golkar L, Ding XZ, Ujiki MB (2007) Resveratrol inhibits pancreatic cancer cell proliferation through transcriptional induction of macrophage inhibitory cytokine-1. J Surg Res 138: 163-169.
- Hong QY, Wu GM, Qian GS (2015) Prevention and management of lung cancer in China. Cancer 121 Suppl 17: 3080-3088
- Ko JC, Syu JJ, Chen JC (2015) Resveratrol Enhances Etoposide-Induced Cytotoxicity through Down-Regulating ERK1/2 and AKT-Mediated X-ray Repair Cross-Complement Group 1 (XRCC1) Protein Expression in Human Non-Small-Cell Lung Cancer Cells. Basic Clin Pharmacol Toxicol 117: 383-391.
- Ma L, Li W, Wang R (2015) Resveratrol enhanced anticancer effects of cisplatin on non-small cell lung cancer cell lines by inducing mitochondrial dysfunction and cell apoptosis. Int J Oncol 47: 1460-1468
- Wang H, Zhang H, Tang L (2013) Resveratrol inhibits TGF-beta1-induced epithelial-to-mesenchymal transition and suppresses lung cancer invasion and metastasis. Toxicology 303: 139-146
- Zhang L, Dai F, Sheng PL (2015) Resveratrol analogue 3,4,4'-trihydroxy-trans-stilbene induces apoptosis and autophagy in human non-small-cell lung cancer cells in vitro. Acta Pharmacol Sin 36: 1256-1265.
- Luo H, Wang L, Schulte BA (2013) Resveratrol enhances ionizing radiation-induced premature senescence in lung cancer cells. Int J Oncol 43: 1999-2006
- Khasraw M, Lassman AB (2010) Advances in the treatment of malignant gliomas. Curr Oncol Rep 12: 26-33
- Lin H, Xiong W, Zhang X (2011) Notch-1 activation-dependent p53 restoration contributes to resveratrol-induced apoptosis in glioblastoma cells. Oncol Rep 26: 925-930.
- Yang YP, Chang YL, Huang PI (2012) Resveratrol suppresses tumorigenicity and enhances radiosensitivity in primary glioblastoma tumor initiating cells by inhibiting the STAT3 axis. J Cell Physiol 227: 976-993
- Li H, Liu Y, Jiao Y (2016) Resveratrol sensitizes glioblastoma-initiating cells to temozolomide by inducing cell apoptosis and promoting differentiation. Oncol Rep 35: 343-351.
- Wang G, Dai F, Yu K (2015) Resveratrol inhibits glioma cell growth via targeting oncogenic microRNAs and multiple signaling pathways. Int J Oncol 46: 1739-1747.
- Chen JC, Chen Y (2006) Resveratrol suppresses angiogenesis in gliomas: evaluation by color Doppler ultrasound. Anticancer Res 26: 1237-1245.
- Zhang W, Murao K, Zhang X (2010) Resveratrol represses YKL-40 expression in human glioma U87 cells. BMC Cancer 10: 1-9.
- Zhang P, Li H, Wu ML (2006) c-Myc downregulation: a critical molecular event in resveratrol-induced cell cycle arrest and apoptosis of human medulloblastoma cells. J Neurooncol 80: 123-131.
- Cilibrasi C, Riva G, Romano G (2017) Resveratrol Impairs Glioma Stem Cells Proliferation and Motility by Modulating the Wnt Signaling Pathway. PLoS One 12: e0169854.
- Xue S, Xiao-Hong S, Lin S (2016) Lumbar puncture-administered resveratrol inhibits STAT3 activation, enhancing autophagy and apoptosis in orthotopic rat glioblastomas. Oncotarget 7: 75790-75799.
- Clark PA, Bhattacharya S, Elmayan A (2017) Resveratrol targeting of AKT and p53 in glioblastoma and glioblastoma stem-like cells to suppress growth and infiltration. J Neurosurg 126: 1448-1460
- Ryu J, Yoon NA, Seong H (2015) Resveratrol Induces Glioma Cell Apoptosis through Activation of Tristetraprolin. Mol Cells 38: 991-997.
- Yang Y, Cui J, Xue F (2016) Resveratrol Represses Pokemon Expression in Human Glioma Cells. Mol Neurobiol 53: 1266-1278.
- Sato A, Okada M, Shibuya K (2013) Resveratrol promotes proteasome-dependent degradation of Nanog via p53 activation and induces differentiation of glioma stem cells. Stem Cell Res 11: 601-610
- Wang C, Hu ZQ, Chu M (2012) Resveratrol inhibited GH3 cell growth and decreased prolactin level via estrogen receptors. Clin Neurol Neurosurg 114: 241-248.
- Lin CJ, Lee CC, Shih Yl (2012) Resveratrol enhances the therapeutic effect of temozolomide against malignant glioma in vitro and in vivo by inhibiting autophagy. Free Radic Biol Med 52: 377-391.
- Gao Z, Xu MS, Barnett TL, Xu CW (2011) Resveratrol induces cellular senescence with attenuated mono-ubiquitination of histone H2B in glioma cells. Biochem Biophys Res Commun 407: 271-276.
- Castino R, Pucer A, Veneroni R (2011) Resveratrol reduces the invasive growth and promotes the acquisition of a long-lasting differentiated phenotype in human glioblastoma cells. J Agric Food Chem 59: 4264-4272.
- Leone S, Cornetta T, Basso E, Cozzi R (2010) Resveratrol induces DNA double-strand breaks through human topoisomerase II interaction. Cancer Lett 295: 167-172.
- Li J, Qin Z, Liang Z (2009) The prosurvival role of autophagy in Resveratrol-induced cytotoxicity in human U251 glioma cells. BMC Cancer 9: 1-9.
- Kao CL, Huang PI, Tsai PH (2009) Resveratrol-induced apoptosis and increased radiosensitivity in CD133-positive cells derived from atypical teratoid/rhabdoid tumor. Int J Radiat Oncol Biol Phys 74: 219-228
- Yu LJ, Wu ML, Li H (2008) Inhibition of STAT3 expression and signaling in resveratrol-differentiated medulloblastoma cells. Neoplasia 10: 736-744.
- American Cancer Society (2012) Cancer Facts & Figures.
- DeSantis C, Siegel R, Bandi P, Jemal A (2011) Breast cancer statistics. CA Cancer J Clin 61: 409-418.
- Khan A, Aljarbou AN, Aldebasi YH, Faisal SM, Khan MA et al. (2014) Resveratrol suppresses the proliferation of breast cancer cells by inhibiting fatty acid synthase signaling pathway. Cancer Epidemiol 38: 765-772.
- Fu Y, Chang H, Peng X (2014) Resveratrol inhibits breast cancer stem-like cells and induces autophagy via suppressing Wnt/beta-catenin signaling pathway. PLoS One 9: e102535
- Kim TH, Shin YJ, Won AJ (2014) Resveratrol enhances chemosensitivity of doxorubicin in multidrug-resistant human breast cancer cells via increased cellular influx of doxorubicin. Biochim Biophys Acta 1840: 615-625.
- Hsieh TC, Wong C, John BD, Wu JM (2011) Regulation of p53 and cell proliferation by resveratrol and its derivatives in breast cancer cells: an in silico and biochemical approach targeting integrin alphavbeta3. Int J Cancer 129: 2732-2743.
- Chatterjee M, Das S, Janarthan M, Ramachandran HK (2011) Role of 5-lipoxygenase in resveratrol mediated suppression of 7,12-dimethylbenz (alpha) anthracene-induced mammary carcinogenesis in rats. Eur J Pharmacol 668: 99-106
- Back JH, Zhu Y, Calabro A (2012) Resveratrol-mediated downregulation of Rictor attenuates autophagic process and suppresses UV-induced skin carcinogenesis. Photochem Photobiol 88: 1165-1172.
- Roy P, Kalra N, Prasad S, George J, Shukla Y, et al. (2009) Chemopreventive potential of resveratrol in mouse skin tumors through regulation of mitochondrial and PI3K/AKT signaling pathways. Pharm Res 26: 211-217.
- Dun J, Chen X, Gao H (2015) Resveratrol synergistically augments anti-tumor effect of 5-FU in vitro and in vivo by increasing S-phase arrest and tumor apoptosis. Exp Biol Med (Maywood) 240: 1672-1681
- Boily G, He XH, Pearce B (2009) SirT1-null mice develop tumors at normal rates but are poorly protected by resveratrol. Oncogene 28: 2882-2893.
- Kim KH, Back JH, Zhu Y (2011) Resveratrol targets transforming growth factor-beta2 signaling to block UV-induced tumor progression. J Invest Dermatol 131: 195-202
- Hao YQ, Huang WX, Feng HX (2013) Study of apoptosis related factors regulatory mechanism of resveratrol to human skin squamous cell carcinoma A431 xenograft in nude mice. 93: 464-468.
- Fabbrocini G, Kisslinger A, Iannelli P (2010) Resveratrol regulates p66Shc activation in HaCaT cells. Exp Dermatol 19: 895-903
- Goldman JM, Melo JV (2003) Chronic myeloid leukemia--advances in biology and new approaches to treatment. N Engl J Med 349: 1451-1464.
- Wu XP, Xiong M, Xu CS (2015) Resveratrol induces apoptosis of human chronic myelogenous leukemia cells in vitro through p38 and JNK-regulated H2AX phosphorylation. Acta Pharmacol Sin 36: 353-361.
- Azimi A, Hagh MF, Talebi M (2015) Time--and Concentration Dependent Effects of Resveratrol on miR 15a and miR16-1 Expression and Apoptosis in the CCRF-CEM Acute Lymphoblastic Leukemia Cell Line. Asian Pac J Cancer Prev 16: 6463-6468.
- Ge J, Liu Y, Li Q (2013) Resveratrol induces apoptosis and autophagy in T-cell acute lymphoblastic leukemia cells by inhibiting Akt/mTOR and activating p38-MAPK. Biomed Environ Sci 26: 902-911.
- Wang XJ, Li YH (2015) Inhibition of human chronic myelogenous leukemia K562 cell growth following combination treatment with resveratrol and imatinib mesylate. Genet Mol Res 14: 6413-6418.
- Kucinska M, Piotrowska H, Luczak MW (2014) Effects of hydroxylated resveratrol analogs on oxidative stress and cancer cells death in human acute T cell leukemia cell line: prooxidative potential of hydroxylated resveratrol analogs. Chem Biol Interact 209: 96-110
- Yaseen A, Chen S, Hock S (2012) Resveratrol sensitizes acute myelogenous leukemia cells to histone deacetylase inhibitors through reactive oxygen species-mediated activation of the extrinsic apoptotic pathway. Mol Pharmacol 82: 1030-1041
- Fan Y, Chen M, Meng J (2014) Arsenic trioxide and resveratrol show synergistic anti-leukemia activity and neutralized cardiotoxicity. PLoS One 9: e105890.
- Zheng M, Chen R, Zhong H (2012) Side-effects of resveratrol in HepG2 cells: reduced pten and increased bcl-xl mRNA expression. Mol Med Rep 6: 1367-1370.
- Athar M, Back JH, Tang X (2007) Resveratrol: a review of preclinical studies for human cancer prevention. Toxicol Appl Pharmacol 224: 274-283.
- Evans HM, Howe PR, Wong RH (2016) Clinical Evaluation of Effects of Chronic Resveratrol Supplementation on Cerebrovascular Function, Cognition, Mood, Physical Function and General Well-Being in Postmenopausal Women-Rationale and Study Design. Nutrients 8: 1-14
- Qiao Y, Sun J, Xia S, Tang X, Shi Y (2014) Effects of resveratrol on gut microbiota and fat storage in a mouse model with high-fat-induced obesity. Food Funct 5: 1241-1249.
- Roberts VH, Pound LD, Thorn SR (2014) Beneficial and cautionary outcomes of resveratrol supplementation in pregnant nonhuman primates. Faseb j 28: 2466-2477.
- la Porte C, Voduc N, Zhang G (2010) Steady-State pharmacokinetics and tolerability of trans-resveratrol 2000 mg twice daily with food, quercetin and alcohol (ethanol) in healthy human subjects. Clin Pharmacokinet 49: 449-454
- Crowell JA, Korytko PJ, Morrissey RL (2004) Resveratrol-associated renal toxicity. Toxicol Sci 82: 614-619.
- Hebbar V, Shen G, Hu R (2005) Toxicogenomics of resveratrol in rat liver. Life Sci 76: 2299-2314
- Kjaer TN, Ornstrup MJ, Poulsen MM (2015) Resveratrol reduces the levels of circulating androgen precursors but has no effect on, testosterone, dihydrotestosterone, PSA levels or prostate volume. A 4-month randomised trial in middle-aged men. Prostate 75: 1255-1263.
- Faghihzadeh F, Adibi P, Hekmatdoost A (2015) The effects of resveratrol supplementation on cardiovascular risk factors in patients with non-alcoholic fatty liver disease: a randomised, double-blind, placebo-controlled study. Br J Nutr 114: 796-803.
- Turner RS, Thomas RG, Craft S (2015) A randomized, double-blind, placebo-controlled trial of resveratrol for Alzheimer disease. Neurology 85: 1383-1391.
- Dash S, Xiao C, Morgantini C, Szeto L (2013) High-dose resveratrol treatment for 2 weeks inhibits intestinal and hepatic lipoprotein production in overweight/obese men. Arterioscler Thromb Vasc Biol 33: 2895-2901
- Wightman EL, Haskell CF, Reay JL (2015) The effects of chronic trans-resveratrol supplementation on aspects of cognitive function, mood, sleep, health and cerebral blood flow in healthy, young humans. Br J Nutr 114: 1427-1437.
Citation: Soo Mi Kim and Sung Zoo Kim (2017) Biological Activities of Resveratrol against Cancer. J Phys Chem Biophys 7: 267. DOI: 10.4172/2161-0398.1000267
Copyright: © 2018 Soo Mi Kim, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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