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Volume 34, Issue 2, Pages 136-141 (April 2010)


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Melanocortin 1 receptor (MC1R), pigmentary characteristics and sun exposure: Findings from a case–control study of diffuse large B-cell and follicular lymphoma

Eleanor V. Kanea, Dan Paintera, Eve Romana, James Allanb, Graham Lawc, Tracy LightfootaCorresponding Author Informationemail address

Accepted 8 January 2010. published online 25 January 2010.

Abstract 

The relationship between skin cancer and non-Hodgkin lymphoma (NHL) suggests common genetic, host or environmental causes. Ultraviolet radiation (UVR), pigmentary characteristics have been linked with both malignancies, and for skin cancer, the melanocortin 1 receptor (MC1R) which influences pigmentation has also been implicated. This paper reports on the relationship between MC1R, skin, hair and eye colour, time spent outdoors, and diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL). Persons carrying MC1R homozygote variant alleles at R151C, R160W, D294H and D84E were more likely to have fair skin, red hair and to spend less time outdoors than those who did not. The variant allele at V92M was associated with FL (odds ratio (OR)=1.61, 95% confidence interval (CI) 1.08–2.39) and the r:wild type genotype with DLBCL (OR=0.58, 95% CI 0.38–0.89). Interactions between MC1R genotypes and skin colour influenced DLBCL risk; the RR genotype increased risk in individuals with medium or dark skin, based on 5 cases and no controls, but decreased risk among those of fair skin. On the whole, DLBCL and FL risk were not related to genetic variation in MC1R, pigmentation or time spent outdoors.

a Epidemiology & Genetics Unit, Department of Health Sciences, Seebohm Rowntree Building, University of York, YO10 5DD, UK

b Department of Biology, University of York, York YO10 5YW, UK

c Division of Biostatistics, Centre of Epidemiology and Biostatistics, Leeds Institute of Genetics, Health and Therapeutics, Worsley Building, University of Leeds, Leeds LS2 9JT, UK

Corresponding Author InformationCorresponding author. Tel.: +44 0 190 432 1881; fax: +44 0 190 432 1899.

PII: S1877-7821(10)00008-1

doi:10.1016/j.canep.2010.01.005


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