Melanocortin 1 receptor variants and skin cancer risk

被引:104
作者
Han, Jiali
Kraft, Peter
Colditz, Graham A.
Wong, Jason
Hunter, David J.
机构
[1] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Program Mol & Genet Epidemiol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
MC1R; skin cancer; melanoma; skin color; hair color;
D O I
10.1002/ijc.22074
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanocortin 1 receptor (MC1R) gene variants are associated with red hair and fair skin color. We assessed the associations of common MC1R genotypes with the risks of 3 types of skin cancer simultaneously in a nested case-control study within the Nurses' Health Study (219 melanoma, 286 squamous cell carcinoma (SCC), and 300 basal cell carcinoma (BCC) cases, and 873 controls). We found that the 151Cys, 160Trp and 294His variants were significantly associated with red hair, fair skin color and childhood tanning tendency. The MC1R variants, especially the 151Cys variant, were associated with increased risks of the 3 types of skin cancer, after controlling for hair color, skin color and other skin cancer risk factors. Carriers of the 151Cys variant had an OR of 1.65 (95% CI, 1.04-2.59) for melanoma, 1.67 (1.12-2.49) for SCC and 1.56 (1.03-2.34) for BCC. Women with medium or olive skin color carrying 1 nonred hair color allele and I red hair color allele had the highest risk of melanoma. A similar interaction pattern was observed for red hair and carrying at least I red hair color allele on melanoma risk. We also observed that the 151Cys variant contributed additional melanoma risk among red-haired women. The information on MC1R status modestly improved the risk prediction; the increase was significant for melanoma and BCC (p, 0.004 and 0.05, respectively). These findings indicated that the effects of the MC1R variants on skin cancer risk were independent from self-reported phenotypic pigmentation. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:1976 / 1984
页数:9
相关论文
共 47 条
[1]  
[Anonymous], 2004, Cancer Facts and Figures
[2]  
Armstrong B K, 1997, Australas J Dermatol, V38 Suppl 1, pS1
[3]   Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair [J].
Bastiaens, MT ;
ter Huurne, JAC ;
Kielich, C ;
Gruis, NA ;
Westendorp, RGJ ;
Vermeer, BJ ;
Bavinck, NJB .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (04) :884-894
[4]   Altered cell surface expression of human MC1R variant receptor alleles associated with red hair and skin cancer risk [J].
Beaumont, KA ;
Newton, RA ;
Smit, DJ ;
Leonard, JH ;
Stow, JL ;
Sturm, RA .
HUMAN MOLECULAR GENETICS, 2005, 14 (15) :2145-2154
[5]   Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma [J].
Box, NF ;
Duffy, DL ;
Irving, RE ;
Russell, A ;
Chen, W ;
Griffiths, LR ;
Parsons, PG ;
Green, AC ;
Sturm, RA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 116 (02) :224-229
[6]   Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair [J].
Box, NF ;
Wyeth, JR ;
OGorman, LE ;
Martin, NG ;
Sturm, RA .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1891-1897
[7]   Sunlight and the onset of skin cancer [J].
Brash, DE .
TRENDS IN GENETICS, 1997, 13 (10) :410-414
[8]   ULTRAVIOLET-B AND MELANOCYTE-STIMULATING HORMONE (MSH) STIMULATE MESSENGER-RNA PRODUCTION FOR ALPHA-MSH RECEPTORS AND PROOPIOMELANOCORTIN-DERIVED PEPTIDES IN MOUSE MELANOMA-CELLS AND TRANSFORMED KERATINOCYTES [J].
CHAKRABORTY, A ;
SLOMINSKI, A ;
ERMAK, G ;
HWANG, J ;
PAWELEK, J .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (05) :655-659
[9]   Production and release of proopiomelanocortin (POMC) derived peptides by human melanocytes and keratinocytes in culture: Regulation by ultraviolet B [J].
Chakraborty, AK ;
Funasaka, Y ;
Slominski, A ;
Ermak, G ;
Hwang, J ;
Pawelek, JM ;
Ichihashi, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1996, 1313 (02) :130-138
[10]   Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype? [J].
Dwyer, T ;
Stankovich, JM ;
Blizzard, L ;
FitzGerald, LM ;
Dickinson, JL ;
Reilly, A ;
Williamson, J ;
Ashbolt, R ;
Berwick, M ;
Sale, MM .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2004, 159 (09) :826-833