Carcinogenesis Advance Access originally published online on February 25, 2006
Carcinogenesis 2006 27(8):1676-1681; doi:10.1093/carcin/bgi381
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Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin
1 Division of Molecular Genetic Epidemiology, German Cancer Research Center Im Neuenheimer Feld 580, 69120 Heidelberg, Germany
2 National Institute of Environmental Health Budapest, Hungary
3 Environmental Health Center Cluj, Romania
4 State Health Institute Banska Bystrica, Slovakia
5 Institute for Chemistry, Karl-Franzens University Graz, Austria
6 Institute of Environmental Medicine, Karolinska Institute Stockholm, Sweden
7 London School of Hygiene and Tropical Medicine London, UK
8 Department of Biosciences at Novum, Karolinska Institute Huddinge, Sweden
*To whom correspondence should be addressed Email: r.kumar{at}dkfz.de
In addition to environmental exposures like UV radiation and, in some cases, arsenic contamination of drinking water, genetic factors may also influence the individual susceptibility to basal cell carcinoma of skin (BCC). In the present study, 529 cases diagnosed with BCC and 533 controls from Hungary, Romania and Slovakia were genotyped for one polymorphism in each of seven DNA repair genes. The variant allele for T241M (C>T) polymorphism in the XRCC3 gene was associated with a decreased cancer risk [odds ratio (OR), 0.73; 95% confidence interval (CI), 0.61–0.88; P = 0.0007, multiple testing corrected P = 0.004]. The risk of multiple BCC was significantly lower among variant allele carriers than in non-carriers (P = 0.04). Men homozygous for the C-allele for E185Q (G>C) polymorphism in the NBS1 gene showed an increased BCC risk (OR, 2.19; 95% CI, 1.23–3.91), but not women (OR, 0.84; 95% CI, 0.49–1.47). In men, the age and nationality adjusted OR for the genotype CC (XRCC3)/CC (NBS1) was 8.79 (95% CI, 2.10–36.8), compared with the genotype TT (XRCC3)/GG (NBS1). The data from this study show overall risk modulation of BCC by variant allele for T241M polymorphism in XRCC3 and gender-specific effect by E185Q polymorphism in NBS1.
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