Journal Article

Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin

Ranjit Kumar Thirumaran, Justo Lorenzo Bermejo, Peter Rudnai, Eugene Gurzau, Kvetoslava Koppova, Walter Goessler, Marie Vahter, Giovanni S. Leonardi, Felicity Clemens, Tony Fletcher, Kari Hemminki and Rajiv Kumar

in Carcinogenesis

Volume 27, issue 8, pages 1676-1681
ISSN: 0143-3334
Published online February 2006 | e-ISSN: 1460-2180 | DOI: http://dx.doi.org/10.1093/carcin/bgi381
Single nucleotide polymorphisms in DNA repair genes and basal cell carcinoma of skin

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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.

Journal Article.  4484 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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