Human Molecular Genetics, 2001, Vol. 10, No. 16 1701-1708
© 2001 Oxford University Press
The melanocortin-1-receptor gene is the major freckle gene
Department of Dermatology and 1Department of Clinical Epidemiology, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, The Netherlands
Ephelides and solar lentigines are different types of pigmented skin lesions. Ephelides appear early in childhood and are associated with fair skin type and red hair. Solar lentigines appear with increasing age and are a sign of photodamage. Both lesions are strong risk indicators for melanoma and non-melanoma skin cancer. Melanocortin-1-receptor (MC1R) gene variants are also associated with fair skin, red hair and melanoma and non-melanoma skin cancer. The purpose of this study was to investigate the relationship between MC1R gene variants, ephelides and solar lentigines. In a large case-control study, patients with melanoma and non-melanoma skin cancer and subjects without a history of skin cancer were studied. In all participants, the presence of ephelides in childhood and solar lentigines by physical examination was assessed according to strict definitions. The entire coding sequence of the MC1R gene was analyzed by single-strand conformation polymorphism analysis followed by sequence analyses. Carriers of one or two MC1R gene variants had a 3- and 11-fold increased risk of developing ephelides, respectively (both P < 0.0001), whereas the risk of developing severe solar lentigines was increased 1.5- and 2-fold (P = 0.035 and P < 0.0001), respectively. These associations were independent of skin type and hair color, and were comparable in patients with and without a history of skin cancer. The population attributable risk for ephelides to MC1R gene variants was 60%, i.e. 60% of the ephelides in the population was caused by MC1R gene variants. A dosage effect was found between the degree of ephelides and the number of MC1R gene variants. As nearly all individuals with ephelides were carriers of at least one MC1R gene variant, our data suggest that MC1R gene variants are necessary to develop ephelides. The results of the study also suggest that MC1R gene variants play a role, although less important, in the development of solar lentigines.
+ To whom correspondence should be addressed. Tel: +31 71 5262421; Fax: +31 71 5248106; Email: j.n.bouwes_bavinck@lumc.nl
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Kvaskoff, S. Mesrine, F. Clavel-Chapelon, and M.-C. Boutron-Ruault Endometriosis risk in relation to naevi, freckles and skin sensitivity to sun exposure: the French E3N cohort Int. J. Epidemiol., August 1, 2009; 38(4): 1143 - 1153. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Tucker Is Sunlight Important to Melanoma Causation? Cancer Epidemiol. Biomarkers Prev., March 1, 2008; 17(3): 467 - 468. [Full Text] [PDF] |
||||
![]() |
I. J. Jackson, P. S. Budd, M. Keighren, and L. McKie Humanized MC1R transgenic mice reveal human specific receptor function Hum. Mol. Genet., October 1, 2007; 16(19): 2341 - 2348. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Beaumont, S. L. Shekar, R. A. Newton, M. R. James, J. L. Stow, D. L. Duffy, and R. A. Sturm Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles Hum. Mol. Genet., September 15, 2007; 16(18): 2249 - 2260. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. L. Norton, R. A. Kittles, E. Parra, P. McKeigue, X. Mao, K. Cheng, V. A. Canfield, D. G. Bradley, B. McEvoy, and M. D. Shriver Genetic Evidence for the Convergent Evolution of Light Skin in Europeans and East Asians Mol. Biol. Evol., March 1, 2007; 24(3): 710 - 722. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Chin, L. A. Garraway, and D. E. Fisher Malignant melanoma: genetics and therapeutics in the genomic era. Genes & Dev., August 15, 2006; 20(16): 2149 - 2182. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Chaudru, K. Laud, M.-F. Avril, A. Miniere, A. Chompret, B. Bressac-de Paillerets, F. Demenais, and The French Familial Melanoma Study Group Melanocortin-1 Receptor (MC1R) Gene Variants and Dysplastic Nevi Modify Penetrance of CDKN2A Mutations in French Melanoma-Prone Pedigrees Cancer Epidemiol. Biomarkers Prev., October 1, 2005; 14(10): 2384 - 2390. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. P. Dellavalle, K. R. Johnson, E. J. Hester, A. M. Deas, S. Mokrohisky, J. G. Morelli, and L. A. Crane Children With Red Hair Have More Freckles but Fewer Melanocytic Nevi: Results From a Cohort Study of 280 Three-Year-Olds Arch Dermatol, August 1, 2005; 141(8): 1042 - 1043. [Full Text] [PDF] |
||||
![]() |
M. T. Landi, P. A. Kanetsky, S. Tsang, B. Gold, D. Munroe, T. Rebbeck, J. Swoyer, M. Ter-Minassian, M. Hedayati, L. Grossman, et al. MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population J Natl Cancer Inst, July 6, 2005; 97(13): 998 - 1007. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Jackson, M. Harland, F. Turner, C. Taylor, P. A. Chambers, J. Randerson-Moor, A. J. Swerdlow, I. dos Santos Silva, S. Beswick, D. T. Bishop, et al. No Evidence for BRAF as a Melanoma/Nevus Susceptibility Gene Cancer Epidemiol. Biomarkers Prev., April 1, 2005; 14(4): 913 - 918. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Sanchez-Mas, L. A. Guillo, P. Zanna, C. Jimenez-Cervantes, and J. C. Garcia-Borron Role of G Protein-Coupled Receptor Kinases in the Homologous Desensitization of the Human and Mouse Melanocortin 1 Receptors Mol. Endocrinol., April 1, 2005; 19(4): 1035 - 1048. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Corre, A. Primot, E. Sviderskaya, D. C. Bennett, S. Vaulont, C. R. Goding, and M.-D. Galibert UV-induced Expression of Key Component of the Tanning Process, the POMC and MC1R Genes, Is Dependent on the p-38-activated Upstream Stimulating Factor-1 (USF-1) J. Biol. Chem., December 3, 2004; 279(49): 51226 - 51233. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. A. Kanetsky, F. Ge, D. Najarian, J. Swoyer, S. Panossian, L. Schuchter, R. Holmes, D. Guerry, and T. R. Rebbeck Assessment of Polymorphic Variants in the Melanocortin-1 Receptor Gene with Cutaneous Pigmentation Using an Evolutionary Approach Cancer Epidemiol. Biomarkers Prev., May 1, 2004; 13(5): 808 - 819. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Duffy, N. F. Box, W. Chen, J. S. Palmer, G. W. Montgomery, M. R. James, N. K. Hayward, N. G. Martin, and R. A. Sturm Interactive effects of MC1R and OCA2 on melanoma risk phenotypes Hum. Mol. Genet., February 15, 2004; 13(4): 447 - 461. [Abstract] [Full Text] [PDF] |
||||
![]() |
E Matichard, P Verpillat, R Meziani, B Gerard, V Descamps, E Legroux, M Burnouf, G Bertrand, F Bouscarat, A Archimbaud, et al. Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure J. Med. Genet., February 1, 2004; 41(2): e13 - 13. [Full Text] [PDF] |
||||
![]() |
R. Kemkemer, S. Schrank, W. Vogel, H. Gruler, and D. Kaufmann Increased noise as an effect of haploinsufficiency of the tumor-suppressor gene neurofibromatosis type 1 in vitro PNAS, October 15, 2002; 99(21): 13783 - 13788. [Abstract] [Full Text] [PDF] |
||||










