Melanocortin receptor 1 variants and melanoma risk: a study of 2 European populations

International Journal of Cancer. Journal International Du Cancer
Dominique SchererR Kumar

Abstract

Variation within the melanocortin receptor 1 (MC1R) gene, that influences phenotypic traits and susceptibility to melanoma, is abundant across the populations. We assessed and compared the risk of melanoma in 2 European populations, German and Spanish, by genotyping MC1R variants through direct DNA sequencing from 1,185 melanoma cases and 1,582 controls. The presence of any variant in both populations was associated with a significantly increased risk of melanoma (odds ratio OR = 1.67, 95% confidence interval CI 1.40-1.99). The population attributable fractions (PAF) associated with the MC1R variants in both populations was over 25%. However, the results showed a statistically significant (p < 0.0001) higher frequency of MC1R variants in the German (70%) than in the Spanish population (60%). The red-hair colour (RHC) variants, though associated with increased risk in both populations, were more common in the German than in the Spanish population (p < 0.0001). Interestingly, non-RHC variants increased the disease risk in the Spanish (OR = 1.60, 95% CI 1.20-2.14) but not in the German population (OR = 1.07, 95% CI 0.80-1.44). Although RHC variants explained a major proportion of the observed PAF in the German population, in the S...Continue Reading

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Related Concepts

Malignant Neoplasm of Skin
MC1R Protein
Dysequilibrium Syndrome
Genetics, Population
Melanoma vaccine
Sequence Determinations, DNA
Hair Diseases
Nested Case-Control Studies
Linkage Disequilibrium
MC1R gene

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