Reach Us +1-947-333-4405
Going Green: The Role of the Green Tea Component EGCG in Chemoprevention | OMICS International
ISSN: 2157-2518
Journal of Carcinogenesis & Mutagenesis

Like us on:

Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Going Green: The Role of the Green Tea Component EGCG in Chemoprevention

Laura Schramm*

Department of Biological Sciences, St. John’s University, NY 11439, USA

*Corresponding Author:
Laura Schramm
St. John’s University
Department of Biological Sciences
8000 Utopia Parkway, Queens
NY 11439, USA
Tel: 718-990-5558
E-mail:[email protected]

Received date: February 23, 2013; Accepted date: May 10, 2013; Published date: May 20, 2013

Citation: Schramm L (2013) Going Green: The Role of the Green Tea Component EGCG in Chemoprevention. J Carcinogene Mutagene 4:142. doi: 10.4172/2157-2518.1000142

Copyright: © 2013 Schramm L. 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.

Visit for more related articles at Journal of Carcinogenesis & Mutagenesis


Tea is one of the most consumed beverages worldwide, and green tea is the least processed from the buds of the Camellia sinensis plant. The most abundant component of green tea is (-)-epigallocatechin-3-gallate (EGCG), which has been the focus of many cell culture, animal and clinical trials, revealing that EGCG possesses antiproliferative, antimutagenic, antioxidant, antibacterial, antiviral and chemopreventive effects. In this review we briefly summarize the mechanism of action(s) of the green tea component EGCG, highlighting recent advances in the epigenetic regulation by EGCG. Additionally, we provide an overview of mouse chemoprevention studies and EGCG chemoprevention clinical trials.


EGCG; Green tea; Cancer; Chemoprevention


Tea is one of the most consumed beverages worldwide, second only to water, and is produced from the buds of the Camellia sinensis plant. The three major tea types, green, oolong and black teas, all have various processing methods. Green tea is the least processed of the teas and contains less caffeine than both oolong and black teas [1,2]. Approximately 78% of the worldwide tea production is black tea, whereas green tea, mainly consumed in China and Japan, constitutes about 20% [1,2]. The tea plant is considered native to south China and is now cultivated in many other countries. The major teaproducing countries are China, India, Japan, Sri Lanka, Indonesia and Central African countries. The synthesis of catechins and flavonoids by Camellia sinesis leaves occur during the day and are temperature dependent. The major catechins, a group of polyphenols, in green tea include: (-)-Epigallocatechin-3-Gallate (EGCG); (-)-Epigallocatecin (EGC); (-)-Epicatechin (EC); and (-)-Epicatechin Gallate (ECG) (Figure 1), EGCG being the most abundant and best studied (Table 1) [2].


Figure 1: Chemical Structures of Major Green Tea Metabolites.
A. Epigallocatechin-3-Gallate (EGCG),
B. Epigallocatechin (EGC),
C. Epicatechin-3-Gallate (ECG),
D. Epicatechin (EC). Functional groups are denoted in red. Structures created using ChemSpider, a free chemical structure database (

Green Tea Constituents Concentration
(mg/8 fl oz)*
Epigallocatechin-3-Gallate (EGCG) 25–106
Epigallocatechin (EGC) 49–113
Epicatechin-3-Gallate (ECG) 4–36
Epicatechin (EC) 6–19

Table 1: Major catechin classes identified in green tea.

Many studies have demonstrated that green tea, particularly EGCG, possesses antiproliferative [3-6], antimutagenic [7,8], antioxidant [9-11], antibacterial [12], antiviral [13,14] and chemopreventive effects [15-23]. Green tea polyphenols, and its major constituent EGCG, have been tested in tissue culture [24-27], animals [3,28-33] and more recently in clinical trials [14,34-38].

In this review we briefly summarize the mechanism of action(s) of the green tea component EGCG, highlighting recent advances in the epigenetic regulation by EGCG. Additionally, we provide an overview of mouse chemoprevention studies and EGCG chemoprevention clinical trials.

Mechanisms of EGCG Action

Numerous tissue culture studies have identified multiple mechanisms for green tea, most notably for EGCG, in chemoprevention. EGCG has been demonstrated to regulate signal transduction pathways including: JAK/STAT [39]; MAPK [40,41]; PI3K/AKT [42-44]; Wnt [45,46]; Notch [47-49]; NF-κB [50-53] and AP-1[41]. Additionally, green tea has been demonstrated to induce a host of tumor suppressor activities such as: p53 [54-57]; p21 [58,59]; p16 [60] and Rb [61] known to play a role in chemoprevention [62-64]. EGCG has also been shown to play a role in regulating a variety of receptors involved in a host of biological functions. For example, EGCG regulates the activity of the 67-KDa laminin receptor, originally identified as part of the Extracellular Matrix (ECM) functions as part of the translational machinery and as a cell surface receptor [65-69]. Moreover, EGCG can regulate activity of the Androgen Receptor (AR) in prostate cancer [70-72] and the Estrogen Receptor (ER) in breast cancer [73,74].

Epigenetic Mechanisms of EGCG

Nutrients and bioactive food components, including green tea, have been demonstrated to induce epigenetic changes, including alterations in histone modifications and DNA methylation (Figure 2) [75,76]. Hypermethylation of promoter regions, CpG islands, is an effective means to silence genes including tumor suppressors, DNA repair enzymes and other genes encoding proteins regulating cell proliferation [28,73,77-79]. Histone acetylation leads to increased gene expression and is regulated by the opposing actions of Histone Acetyltransferases (HATs) and Deacetylases (HDACs), which have been demonstrated to be influenced by dietary compounds [80].


Figure 2: Epigenetic mechanisms regulating gene expression.
A. Acetylation of histones by histone acetyltransferases (HATs) leads to increased gene expression, whereas histone deacetylation by histone deacetyltransferases (HDACs) leads to decreases in gene expression.
B. Methylation of DNA by DNA methyl transferases (DNMTs) leads to gene silencing.

In eukaryotic cells, RNA polymerase II and III promoter activity is inhibited by promoter specific methylation [81], which occurs through the actions of DNA methyl transferases (DNMT1, DNMT3a, DNMT3b) [82]. EGCG has been demonstrated to inhibit the activity of DNMT1 [83]. The activity of RNA polymerase III has been shown to be inhibited by EGCG [84], and more recently RNA polymerase III transcription is modulated by DNMT1 and DNMT3a [85], suggesting that regulation of RNA polymerase III transcription by EGCG may occur via DNA methyltransferases. Also, the methylation of the Gluthathione-S-Transferase Pi (GSTP1) promoter is a molecular marker for prostate cancer and has been demonstrated in over 90% of invasive cancers of prostate origin and 70% of Prostatic Intraepithelial Neoplasia (PIN) lesions [86]. The loss of GSTP1 expression correlates with decreased prostate cancer survival [87]. Green tea polyphenol treatment inhibited DNMT activity, effectively reactivating GSTP1 expression which may be beneficial in patients with prostate cancer [88]. Recent studies have demonstrated that EGCG induces epigenetic changes modulating hTERT activity, the catalytic subunit of telomerase, which is overexpressed in 90% of cancers [89,90] through inhibition of DNMT and HAT activity [91]. Furthermore, EGCG has been demonstrated to inhibit promoter methylation of the tumor suppressors’ p16 and p15, thereby restoring expression in colon cancer cells [92]. EGCG also inhibits the methylation of the promoter region of the p21/waf1 and Bax genes in prostate cancer cells [93]. Taken together, these data suggest that dietary compounds, such as green tea, can modulate epigenetic regulation of gene expression and have the potential to play a pivotal role in chemoprevention [94].

EGCG as a Chemopreventive in Mouse Models

“Cancer chemoprevention” was a term first introduced in 1976 by M. Sporn, who defined cancer chemoprevention as the prevention of the occurrence of cancer by the oral administration of one or multiple compounds [95]. During the compilation of this manuscript, a query of EGCG and chemoprevention in the PubMed database indicates there are 154 published studies on EGCG as a chemopreventive agent in mouse cancer models. EGCG exhibited chemopreventive activities in lung, prostate, breast, colon, oral and skin cancers in mouse models.

One study demonstrated that the differential expression of 88 genes in lung tumors compared with normal tissues was reversed by green tea treatment in A/J mice. These authors also identified 17 genes that are altered by tea treatments in both normal lungs and lung adenomas, suggesting that these genes could be used as markers for tea exposure [96]. Also, researchers have demonstrated the prevention of mammary carcinogenesis in C3H/OuJ mice by EGCG [97]. Green tea inhibits development and progression of prostate cancer in transgenic adenocarcinoma of the mouse prostate [98-100]. Additionally, colon cancer prevention activity by tea polyphenols has been clearly demonstrated in mouse models, but results from studies in rat models have yielded inconsistent results [101]. EGCG has also been successful in inhibiting oral cavity cancer in C3H/HeJ mice [102]. Taken together, these data suggest that green tea, especially EGCG, exhibits chemopreventive properties in mouse models.

EGCG as a Chemopreventive in Clinical Trials

The 2013 cancer statistics reveal that cancer incidences have declined slightly for men, 0.6%, and remained unchanged for women during 2005-2009 [103], suggesting that more efforts are needed to develop chemoprevention therapies. In 1987, EGCG’s chemopreventive effect was first reported when the inhibitory effects of EGCG on teleocidininduced tumor promotion in mouse skin was observed [104]. There is an increasing amount of evidence that has been presented, indicating that green tea may be chemopreventive [105].

For example, clinical trials in prostate cancer patients suggest that green tea may play a role as a chemopreventive agent in progression [36]. In Japan, a study including 49,920 males aged 40-69, found that drinking greater than 5 cups of green tea per day showed a reduced risk of developing advanced prostate cancers [106]. Additionally, a double blind randomized trial of 60 patients recently diagnosed with High Grade Prostatic Intraepithelial Neoplasia (HG-PIN), who have a 30% likelihood of developing one year post HG-PIN diagnosis, was treated with green tea catechins or placebo [107]. The study showed that 30% of participants receiving the placebo developed HG-PIN after one year compared to the 3% receiving green tea catechins [107]. Two year follow up studies were performed and indicated that green tea catechin prevention was long lasting [108].

Prostate cancer is not the only cancer for which green tea catechins have been demonstrated as a chemopreventive. Recently, studies provide evidence that EGCG has potential to halt carcinogenesis in patients with Head Neck And Squamous Cell Carcinoma (HNSCC) [109]. In a phase II trial, patients with oral premalignant lesions were administered Green Tea Extract (GTE) capsules containing 13.2% of EGCG three times a day for 12 weeks had statistically significant clinical response rates in comparison to low doses of GTE [109]. Additionally, a colon cancer chemoprevention pilot study demonstrated that administration of 500 mg of GTE tablet containing 52.5 mg of EGCG three times daily for 12 months significantly (P < 0.05) inhibited the incidence of secondary metachronous colon adenomas [110].

There have been clinical and epidemiological studies yielding conflicting results for a variety of cancers involving green tea, including: breast [111-113]; colorectal [114,115]; esophageal [116] and lung [117] cancers. In the case of breast cancer, a very large cohort study involving the pooled analysis of two studies with 35,004 Japanese women showed no association between green tea intake and breast cancer risk [112]. These results contradict a previous study examining the association between regular green tea consumption prior to breast cancer incidence and reoccurrence and concluded green tea consumption may be preventive against recurrence of early breast cancer [111]. Colorectal cancer clinical studies have also reported conflicting results. In one study evaluating the association between green tea consumption and colorectal cancer 69,710 Chinese women aged 40 to 70 years were interviewed to ascertain green tea consumption habits and during the six year follow up a dose response protective effect of green tea was noted for women and colorectal cancer [114]. The same protective effect was not as clear cut for male green tea drinkers and colorectal cancer [115]. Mixed results have been reported for esophageal cancers. It appears that the chemopreventive effects of green tea can be counteracted by high temperatures [116]. Also, fewer well controlled clinical studies have looked at chemoprevention of lung cancer by green tea have been undertaken. However, a few well controlled studies indicate that green tea and black tea increased the risk of lung cancer [117].

It is important to note that epidemiological studies data have been used to determine the association between green tea consumption and cancer risk and selected confounding results may be accounted for by differences in lifestyle, diet and genetic variability. Many of the green tea epidemiology studies are done with Asian populations where tea drinking is associated with cigarette smoking and alcohol consumption [118]. Therefore, larger clinical studies controlling for confounders may be warranted to determine if green tea can be used as a general chemopreventive.

Importantly, there were no serious adverse effects documented in any of these green tea clinical trials. The sample sizes for controlled clinical trials are small but nonetheless significant. Even with conflicting epidemiological studies, these small and significant clinical trials further demonstrate the need for larger-scale EGCG chemoprevention studies for a subset of cancers to determine if green tea should be included in the American Recommended Daily Amounts (RDA) as part of a healthy lifestyle.

Green tea has been demonstrated to have a plethora of health benefits including; lowering blood pressure [119], increasing insulin sensitivity [119] and cardiovascular benefits [120]. In addition, EGCG, the major component of green tea, has been implicated in a host of biochemical pathways controlling cell growth and proliferation [121,122]. Animal cancer models have demonstrated that EGCG can inhibit tumorigenesis. Although there have been conflicting results for a variety of cancers such as breast [111-113]; colorectal [114,115]; esophageal [116] and lung [117] cancers there is strong evidence from clinical trials for prostate [31,107,108], oral [109] and colon cancer [110] showing promise for the use of green tea for cancer chemoprevention.

Recent 2013 cancer statistics [103] reveal that the incidence of cancer has remained relatively constant, suggesting that larger scale carefully controlled Chemopreventivetive clinical studies using natural products, such as green tea catechins, are warranted.


This work is supported in part by the National Institute of Health AREA grant 1R15CA133842-01A1 (LS). We thank Dr. Stephanie Cabarcas, Gannon University, for critically reading this manuscript.


Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Article Usage

  • Total views: 12171
  • [From(publication date):
    June-2013 - Dec 17, 2018]
  • Breakdown by view type
  • HTML page views : 8367
  • PDF downloads : 3804

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2018-19
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri and Aquaculture Journals

Dr. Krish

[email protected]

+1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals


[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry


[email protected]

1-702-714-7001Extn: 9042

© 2008- 2018 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version