Reach Us +1-947-333-4405
Role of Mc1r in UV-Induced Melanoma in Animal Models | 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
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Role of Mc1r in UV-Induced Melanoma in Animal Models

Agnieszka Wolnicka-Glubisz*

Department of Biophysics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland

*Corresponding Author:
Agnieszka Wolnicka-Glubisz
Department of Biophysics, Faculty of Biochemistry
Biophysics and Biotechnology, Jagiellonian University
ul.Gronostajowa 7, 30-387 Kraków, Poland
Tel: 48-12-6646526
Fax: 48-12-6646901
E-mail: [email protected]

Received date: October 22, 2014; Accepted date: November 27, 2014; Published date: November 30, 2014

Citation: Wolnicka-Glubisz A (2014) Role of Mc1r in UV-Induced Melanoma in Animal Models. J Carcinog Mutagen 5:200. doi: 10.4172/2157-2518.1000200

Copyright: © 2014 Wolnicka-Glubisz A, 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.

Visit for more related articles at Journal of Carcinogenesis & Mutagenesis


The role of UV and pigmentation are very difficult to control for in human studies, and mechanisms difficult to infer based on statistical association with melanoma. The animal models are not representative of the human situation. But on the other hand, animal studies can be useful for basic studies that will ultimately help in building up a picture of the overall network of in vivo cellular behavior and intra and inter cellular pathways contributing to melanoma progression and the effects (or not) of UV radiation in individuals with MC1R variants. This review describes that, although the Mc1r is a determinant of coat color phenotype as the MC1R is a determinant of hair and skin color in humans, deficiency of the Mc1r in mice is associated with a paradoxical lower incidence of melanoma.


Mc1r; melanoma; UV; HGF; c-Met; B-Raf; mouse model

MC1R and Mc1r

The melanocortin-1 receptor (MC1R) is a member of the G-protein-coupled receptor (GPCR) superfamily the ligand for which, alpha-melanocyte stimulating hormone (α-MSH), is derived from the proopiomelanocortin (POMC) precursor protein [1,2]. MC1R present in melanocyte membrane is involved in melanogenesis where it regulates the amount and type of melanin production and thus human skin phototype and its sensitivity to UV induced damage [3,4]. There are two main types of melanin: pheomelanin (red/yellow) and eumelanin (brown/black), which are derived from the same precursor dopaquinone that is formed following oxidation of tyrosine by tyrosinase [5,6]. However while synthesis of eumelanin requires MC1R activity, the synthesis of pheomelanins is a default pathway which proceeds in the absence of MC1R signaling [7]. In pigmented tissues such as skin melanin is present as mixtures or copolymers of both types [8]. MC1R engagement with its ligands, α-MSH or adenocorticotropic hormone (ACTH) activates adenyl cyclase (AC), resulting in cAMP production, which leads to phosphorylation of cAMP responsive-element-binding protein (CREB), a member of the transcription factor family [6]. CREB activates microphthalmia transcription factor (MITF) which activates the enzyme tyrosinase [6]. The MC1R coding region in humans is highly polymorphic with at least 30 allelic variants, most of which result from a single amino-acid substitution [8]. Also in other mammals similar single polymorphisms as well as mutations causing frame shifts and truncated Mc1r variants have been found [9].

In mouse hair, signaling through the Mc1r acts as a control point for determining the eumelanin/phaeomelanin ratio and its loss of function or mutations results in yellow coat color [10]. The hair of the Mc1r mouse is often used in EPR analysis as a natural standard of pheomelanin although it should be noted that it does not contained pure pheomelanin [11,12]. In the recessive yellow mouse (Mc1re/e, extension mutation), a frame shift mutation in the Mc1r gene causes deletion of a single nucleotide at position 549 of the open reading frame and results in a premature stop after 12 additional codons, the result of which is premature termination in the fourth trans-membrane domain of the receptor protein making it unable to couple to AC and activate cAMP [13,14]. The Mc1r receptor in the mouse thus differs from the human polymorphisms in MC1R which encode a complete receptor, albeit one with altered function, although there is 76% identity in amino acid sequence. In the mouse Mc1r the receptor is truncated and the ability to engage cAMP is totally absent.

There are differences between MC1R and Mc1r. Mc1r required a higher concentration of α-MSH [13] and is less sensitive to exogenous ligands like agouti signaling protein (ASP) which acts as an extracellular antagonist of Mc1r signaling [14,15]. The difference in potency is compensated in vivo by expression of a higher number of Mc1r receptors on mouse than on human melanocytes [16,17]. Moreover, it seems that signaling by Mc1r is largely ligand-independent in vivo, as loss of POMC, the precursor of α-MSH, in C57BL/6 mice preserved eumelanin hair pigmentation [18], while most individuas that lack POMC have red hair [19,20].

UV-Induced Melanoma

Damage to epidermal melanocytes plays a critical role in the development of malignant melanoma (CMM), which occurs in skin, but is also found in other parts of the body, including the bowel and the eye (uveal melanoma). It is one of the most lethal types of cancers. A causal role for solar UV exposure, in etiology of cutaneous melanoma is widely accepted. UV radiation, that reaches the earth surface consists mainly of UVA (95%; 320-400 nm), and about 5% of UVB (280-320 nm). UVC (200-280 nm) is completely absorbed by the earth’s atmosphere. Stratospheric ozone depletion, leads to increases doses of UVB transmitted to the Earth, which increases the risk for skin cancer including melanoma [22]. Epidemiologic studies indicate increased susceptibility of children to UV-induced melanoma [23,24]. Studies on a mouse model for UV-induced melanoma, confirmed that exposure to UV of neonatal but not adult HGF/SF(Hepatocyte growth factor/scatter factor) transgenic mice resulted in development of melanoma within a year of treatment [25-28]. HGF/SF transgenic mouse in which mouse HGF/SF cDNA sequences were overexpressed by virtue of a mouse metallothionein (MT) gene promoter and associated locus control regions [29,30], has an increased number of extra-follicular dermal melanocytes in the trunk skin, that imitate human skin (melanocytes are present in the skin, in contrast to wild type mouse which has melanocytes present only in hair follicles). In contrast to other animal model, in which only dermal-animal melanoma occurs, neonatal HGF transgenic mice are susceptible to UV-induced melanoma which, uniquely among melanoma mouse models, recapitulate the histopathology of human disease, namely superficial spreading melanoma (SSM) [25-28]. The mechanism of juvenile susceptibility to melanoma is not well known. However our studies on HGF/SF transgenic mice suggest that the immaturity of melanocytes in the skin and the profound defect in the immune response, of UV-induced DNA damage, play an important role in the susceptibility of juvenile mice to UV-induced malignant melanoma [24,28].

Mc1r and Immune System

In addition to cutaneous and hair follicle melanocytes, keratinocytes and fibroblasts, MC1R expression was also found on macrophages, lymphocytes, neutrophils and dendritic cells [3], suggesting a role not only in skin physiology and melanogenesis but also in inflammation. Melanotropins have been reported to possess anti-inflammatory effects in many experimental models of acute and chronic inflammation, including bowel diseases, allergy and others [31,32]. MC1R is subject to regulation by a variety of paracrine and/or autocrine factors that are synthesized in response to UV exposure of the skin such as α-MSH and ACTH, both derived from POMC, and which protect from UV induced DNA damage and apoptosis [3,32-34]. Most of the studies to date have focused on the anti-inflammatory properties of α-MSH from which it has been concluded that lack of MC1R may increase UV sensitivity [35]. There is ample published evidence that UV upregulates α-MSH in keratinocytes and in melanocytes [36]. UVB has also been elegantly demonstrated to upregulate expression and protein levels of POMC in cultured human skin explants [37]. There is evidence that UV upregulates α-MSH in human skin in vivo. Holzmann et al. [38] reported increased levels of circulating both α-MSH and ACTH in humans in response to UVA irradiation in fair-skinned individuals [38]. In mouse skin Cui et al. [40] found that UVB irradiation of mice increased epidermal POMC protein levels in a p53 dependent manner, consistent with their in vitro studies. The total UVB dose used was 2 kJ/m2 (40 J/m2/day 5 days a week for 10 weeks). In the same study these investigators showed increased α-MSH in cultured human foreskins irradiated with UVC (254 nm germicidal lamp) [39] although it should be noted that 254 nm UVC is not a component of sunlight and thus has limited biologic relevance. The MC1R has been suggested as the receptor responsible for the anti-inflammatory effects of α-MSH and related peptides via inhibition of NF-κB activation [40,41] and protection of IκBα degradation [42]. This results in reduction of the expression of pro-inflammatory cytokines [42] and adhesion molecules [41], therefore affecting the humoral and cellular phases of inflammation [43,44]. Further, Grabbe et al. [45] found that α-MSH decreased contact hypersensitivity and induced immune tolerance in mice, indicating an immunosuppressive role [45].

However, there are inconsistent studies using Mc1re/e yellow mice with a deficiency in Mc1r to investigate the effects of the Mc1r on inflammation and immunity. Using an model of inflammatory peritonitis, Getting et al. [46] found that Mc3r not Mc1r was responsible for the anti-inflammatory effect [46]. In contrast, Maaser et al. [47] found a crucial role for Mc1r in experimental colitis [47]. We have recently demonstrated, however, that lack of Mc1r in mice did not alter an inflammatory response to UV in their skin. For all tested groups of mice: C57BL/6-c (albino),C57BL/6-Mc1re/e (yellow), and C57BL/6 (black) formation of DNA damage as CPD, edema, determined as increase in skin thickness, and infiltrating neutrophils as a percentage of total skin cells after UV irradiation at selected time points remained similar, suggesting that Mc1r does not influence the inflammatory response in mice. We also found that lack of Mc1r did not alter either neonatal immune tolerance or UV immunosuppresion [48]. Our findings were confirmed by other researchers [see commentaries in Experimental Dermatology [49,50].

MC1R and Susceptibility to Melanoma

In human melanoma MC1R polymorphisms are well described as significantly increasing melanoma risk. However only some of these polymorphisms, such as R151C, R160W and D249H that encode hypomorphic mutants that are unable to either bind ligand or activate AC are associated with red hair in a Caucasian population [9,51] and these show the highest risk for melanoma. The “red-head” phenotype (phototype I) is defined not only by hair color but also by light skin, poor tanning ability and sensitivity for sunburn [52] and increased skin cancer including melanoma susceptibility [35,53-55]. Studies on human melanocytes derived from individuals with one of these three mutations showed that loss of function in the MC1R gene sensitizes their melanocytes to UV induced DNA damage and thereby increased its susceptibility to UV induced skin cancer [35,53,55]. However no clear correlation with polymorphisms in MC1R and erythema induced by UVB have been proved [56-58]. The function of human MC1R variants are also extremely diverse, and it seems that different human MC1R variants may affect different melanocyte pathways.

However studies on mouse models described below show diverse effects of Mc1r on melanoma. While lack of the Mc1r in Mc1re/e mice with the B-Raf V600E mutation increased development of melanoma [59], in a mouse model with HGF/SF overexpression mice homozygous for the Mc1r (e/e) mutation with deficient Mc1r signaling, do not develop melanoma [28]. The human MC1R polymorphisms that confer increased melanoma risk yield a receptor with the potential to retain some function which is lacking in recessive yellow mice, where the Mc1r receptor loses all signaling [28]. Moreover the effects on melanoma may not be specific to the particular (e) mutation. For instance Gray Lipizzaner horses carrying a loss-of-function mutation in ASIP (agouti signaling protein) that results in higher levels of Mc1r had a higher incidence of melanoma, implying that increased Mc1r signaling promotes melanoma in these animals [60]. Along these lines, in the Sinclair Swine pig model of melanoma, while black pigs are melanoma-prone, yellow pigs, that are thought to carry either MC1R or ASIP mutations, are resistant [61].

Mc1r and HGF

HGF is the only known ligand of the c-Met receptor (receptor tyrosine kinase). Upon HGF binding, the c-Met receptor can activate various signaling pathways including AKT/PI3K/mTOR, RAS/MAPK and STAT pathways [62] which are highly relevant to melanoma. Aberrant c-Met activation correlates with hyperproliferation, metastasis, tumour angiogenesis and poor prognosis in various human cancers.

Pigmented, black transgenic HGF/SF neonatal mice are more susceptible than albino HGF/SF animals to melanoma, notably to UVA-induced melanoma, suggested to be as a result of oxidative interactions between UVA and eumelanin [12,27]. HGF does not affect melanin synthesis but increases the number of extra-follicular melanocytes resulting in a hyperpigmented phenotype [12,27]. Interestingly while overexpression of HGF increases the number of extra-follicular melanocytes in the trunk skin of FVB and C57-BL/6 mice, which further increase with mouse age, this does not occur in HGF transgenic e/e mice. C57BL/6-Mc1re/e-HGF mice had few extra-follicular melanocytes, even though transgenic HGF and c-Met were expressed. Both C57BL/6-Mc1re/e and C57BL/6-Mc1re/e-HGF have yellow hair and black eyes, and similar amounts of pheomelanin [28]. Lack of melanomas in C57BL/6-Mc1re/e-HGF mice, either in response to UV radiation or spontaneously is consistent with this deficiency of extra-follicular melanocytes [28]. The importance of Mc1r in the extrafollicular survival of melanocytes complements the findings of Chou et al. 2013 who showed that in wild-type mice, Mc1r played an important role in migration of melanocytes from the hair follicle to the epidermis after wounding or UV radiation, a process that does not require transgenic HGF [63]. In our studies, heterozygous C57BL/6-Mc1re/+-HGF mice, which were indistinguishable from Mc1r competent C57BL/6-Mc1r+/+-HGF with similar numbers of dermal melanocytes and eumelanin levels in the skin, nevertheless produced significantly fewer melanomas. Impaired melanoma formation in these heterozygous animals indicates that a previously unrecognized pigment independent interaction between c-Met and Mc1r interaction is necessary for melanoma in this model [28]. It can be speculated that a molecule that regulates signaling pathways of Mc1r and c-Met, is PTEN (phosphatase and tensin homolog) may be responsible. Studies on melanoma and other cancers such as hepatocellular carcinoma and epithelioid sarcoma, show that PTEN can inhibit both PI3K/AKT/mTOR and HGF/c-MET pathways [64,65]. PTEN loss plays an important role in melanoma [65]. Cao et al. show a UVB-dependent interaction between human MC1R and PTEN, a negative regulator of AKT, that protects PTEN from degradation thus limiting AKT activation [67]. Polymorphisms in MC1R show to impair UV-induced binding to PTEN, resulting in senescence in cultured melanocytes [67]. Therefore it is possible that in heterozygous C57BL/6-Mc1r-e/+ -HGF transgenic mice, due to lower expression of Mc1r, PTEN can play important role in inhibition of UV-induced melanoma but this remains to be established.

Mc1r and BRAF

B-RAF, a member of the Raf kinase family of growh signal transduction protein kinases, is a key component of MAPK pathway (mitogen- activated protein kinases, also known as the Ras-Raf-MEK-ERK pathway), which regulates cell proliferation and differentiation. Despite the fact that B-RAF mutation occurs both in melanoma (60-80%), and in pigmented lesions [68, 69], the role of UV damage in BRAF mutation remains unknown. Studies of Cao et al. showed a synergism between MC1R variants and B-RAFV600E in cellular transformation of genetically engineered human immortalized melanocytes [67], but an association between MC1R polymorphisms and B-RAF mutations in human melanoma is not well established, and it has been reported by some groups but not by others [70-72]. Mitra et al. [59] found that ,in a mouse model carrying the B-Raf V600E mutation, spontaneous melanomas occurred in Mc1r deficient (C57BL/6-B-Raf CA- Mc1re/e) yellow mice due to the presence of phaeomelanin [59]. However there was no information on UV melanomas in this model. In contrast, no mutations in B-Raf were found in HGF-transgenic mouse tumors (unpublished observations, 73). Moreover, HGF/SF does not affect the quality of melanin, nor the efficiency of melanogenesis, but only the number and localization of melanocytes. In contrast to C57BL/6-HGF/SF transgenic mice, C57BL/6-B-Raf CA mice do not have extra-follicular melanocytes and arising melanomas are exclusively dermal without epidermal component. Recent studies have shown that the role of HGF in melanoma is not dependent on activated B-RAF signaling in human melanomas, and that HGF can mediate escape from B-RAF inhibition through activation of the MAPK and PI3K-AKT pathways [74,75]. Therefore the effect of the Mc1re/e mutation on melanoma in mouse models not dependent on B-RafV600E or HGF should be established.


Since melanoma is one of the most malignant tumors and is resistant to many traditional therapies, the hope lay in recently introduced molecularly targeted therapies in which mutated genes and impaired pathways are blocked by specific inhibitors. Notably B- RAF inhibitors have been used with partial success and use of c-Met inhibitors has been proposed. However for understanding and better efficiency of therapeutic procedures more extended mechanistic studies on animal models are necessary.


I would like to thank Professor Frances Noonan and Professor Edward De Fabo for careful proofreading of the manuscript and critical discussion.


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

Share This Article

Article Usage

  • Total views: 12281
  • [From(publication date):
    December-2014 - May 25, 2019]
  • Breakdown by view type
  • HTML page views : 8467
  • PDF downloads : 3814