A specific RAD51 haplotype increases breast cancer risk in Jewish non-Ashkenazi high-risk women

Eur J Cancer. 2006 May;42(8):1129-34. doi: 10.1016/j.ejca.2005.09.035. Epub 2006 Apr 18.

Abstract

While the precise genes involved in determining familial breast cancer risk in addition to BRCA1/2 are mostly unknown, one strong candidate is RAD51. Jewish non-Ashkenazi women at high-risk for breast/ovarian cancer and ethnically matched controls were genotyped using four single nucleotide polymorphisms spanning the RAD51 genomic region, and the resulting haplotypes were constructed using the GERBIL algorithm. A total of 314 individuals were genotyped: 184 non-Ashkenazi high-risk women (119 with breast cancer), and 130 unaffected, average-risk ethnically matched controls. Using GEBRIL, three frequent haplotypes were constructed. One of the haplotypes (TGTA - coined haplotype 3) was present in 7.3% (19/260 haplotypes) of controls (n=130) and in 16.8% (40/238 haplotypes) of high-risk breast cancer patients (n=119, P=0.001). A specific RAD51 haplotype is more prevalent among non-Ashkenazi Jewish high-risk women than in average-risk population.

MeSH terms

  • Breast Neoplasms / genetics*
  • Case-Control Studies
  • Female
  • Genes, BRCA1
  • Genes, BRCA2
  • Genotype
  • Haplotypes
  • Heterozygote
  • Humans
  • Jews / genetics*
  • Middle Aged
  • Mutation / genetics
  • Odds Ratio
  • Rad51 Recombinase / genetics*
  • Risk Factors

Substances

  • Rad51 Recombinase