Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8455836 | Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis | 2014 | 8 Pages |
Abstract
We conducted a case-control study to investigate the possible association between the head and neck cancer (HNC) and genetic variability of Rad51C tumor suppressor gene. Eight polymorphic sites spanning over non-coding regions of Rad51C promoter, exon 1 and intron 1 were genotyped in 81 HNC cases and 156 healthy controls using the real-time PCR technique. One investigated site turned out to be not polymorphic, while among the remaining seven sites a significant HNC risk-increasing effect was found for rs16943176 (c.-118G > A), rs12946397 (c.-26C > T) and rs17222691 (c.145 + 947C > T) on both allelic (OR = 1.8; p < 0.05) and genotypic (OR = 2.0; p < 0.05) level. Furthermore, our data seem to provide marginal evidence, that this effect might possibly be confined to women only (OR = 2.8; p = 0.05 for allelic and OR = 3.7; p = 0.05 for genotypic comparisons). These SNPs were found to co-segregate together forming two distinct, HNC risk-modulating haplotypes. The genetic variability of Rad51C might thus be of relevance with respect to HNC risk.
Keywords
NHEJHWEHBOCIQRDSBsICLSHNSCCRAD51C5′ Untranslated region5′UTR95%CIInterstrand cross-linksAdenocarcinomaHardy–Weinberg equilibriumhereditary breast/ovarian cancerdouble strand breaksnon-homologous end joining95% confidence intervalinterquartile rangeodds ratioHomologous recombinationHead and neck squamous cell carcinoma
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Cancer Research
Authors
Peter Gresner, Jolanta Gromadzinska, Ewa Twardowska, Konrad Rydzynski, Wojciech Wasowicz,