MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population

被引:135
作者
Landi, MT
Kanetsky, PA
Tsang, S
Gold, B
Munroe, D
Rebbeck, T
Swoyer, J
Ter-Minassian, M
Hedayati, M
Grossman, L
Goldstein, AM
Calista, D
Pfeiffer, RM
机构
[1] NCI, Genet Epidemiol Branch, Div Canc Epidemiol & Genet, DHHS,NIH, Bethesda, MD 20892 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] NCI, Lab Mol Technol, SAIC, DHHS,NIH, Frederick, MD USA
[4] NCI, Lab Genom Divers, SAIC, DHHS,NIH, Frederick, MD USA
[5] Johns Hopkins Univ, Dept Biochem, Baltimore, MD USA
[6] Maurizio Bufalini Hosp, Dermatol Unit, Cesena, Italy
关键词
D O I
10.1093/jnci/dji176
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Melanoma risk factors include fair pigmentation, multiple nevi, low DNA repair capacity, and CDKN2A or CDK4 mutations. Variants of the melanocortin-1 receptor (MCIR) gene have been associated with fair pigmentation and melanoma risk, and a polymorphism of the Agouti Signaling Protein (ASIP) gene has been associated with dark pigmentation. We examined MCIR and ASIP genotypes in relation to phenotypic characteristics, sporadic and familial melanoma risk, and melanoma thickness as an indicator of disease progression in a Mediterranean population. Methods: We studied 267 melanoma patients and 382 control subjects from a case-control study and a family study in northeastern Italy. Host factors were assessed by physical examination, questionnaire, spectrophotometer, and minimal erythema dose measurement. MC1R was sequenced, ASIP was genotyped, and DNA repair capacity was measured by the host-cell reactivation assay. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated by logistic regression models. Effect modification of the association between MCIR and melanoma risk by phenotypic characteristics and DNA repair capacity was also assessed. All statistical tests were two-sided. Results: Carrying MCIR variant alleles was associated with a two- to fourfold increase in risk of both sporadic and familial melanoma compared with carrying wild-type MCIR, particularly in individuals carrying multiple variant alleles (OR 3.9; 95% CI = 3.3 to 4.6). This association was stronger in individuals with fewer additional risk factors (those with dark skin or few nevi). MC1R variant allele carriers were also three to four times more likely than were non-carriers to have thick melanomas. The ASIP polymorphism was not associated with pigmentation, nevi, or melanoma risk. Conclusions: MCIR was associated with melanoma risk and progression in a Mediterranean population, particularly in the absence of other strong risk factors, such as freckling or many nevi.
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页码:998 / 1007
页数:10
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