RAD51B in Familial Breast Cancer
- Publisher: Public Library of Science
Common variation on 14q24.1, close to RAD51B, has been associated with breast cancer: rs999737\ud and rs2588809 with the risk of female breast cancer and rs1314913 with the risk of male breast\ud cancer. The aim of this study was to investigate the role of RAD51B variants in breast cancer\ud predisposition, particularly in the context of familial breast cancer in Finland. We sequenced the\ud coding region of RAD51B in 168 Finnish breast cancer patients from the Helsinki region for\ud identification of possible recurrent founder mutations. In addition, we studied the known rs999737,\ud rs2588809, and rs1314913 SNPs and RAD51B haplotypes in 44,791 breast cancer cases and 43,583\ud controls from 40 studies participating in the Breast Cancer Association Consortium (BCAC) that\ud were genotyped on a custom chip (iCOGS). We identified one putatively pathogenic missense\ud mutation c.541C>T among the Finnish cancer patients and subsequently genotyped the mutation in\ud additional breast cancer cases (n = 5259) and population controls (n = 3586) from Finland and\ud Belarus. No significant association with breast cancer risk was seen in the meta-analysis of the\ud Finnish datasets or in the large BCAC dataset. The association with previously identified risk\ud variants rs999737, rs2588809, and rs1314913 was replicated among all breast cancer cases and also\ud among familial cases in the BCAC dataset. The most significant association was observed for the\ud haplotype carrying the risk-alleles of all the three SNPs both among all cases (odds ratio (OR): 1.15,\ud 95% confidence interval (CI): 1.11-1.19, P = 8.88 x 10-16) and among familial cases (OR: 1.24,\ud 95% CI: 1.16-1.32, P = 6.19 x 10-11), compared to the haplotype with the respective protective\ud alleles. Our results suggest that loss-of-function mutations in RAD51B are rare, but common\ud variation at the RAD51B region is significantly associated with familial breast cancer risk.
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