A functional link between FOXA1 and breast cancer SNPs

Breast Cancer Res. 2013 Feb 18;15(1):303. doi: 10.1186/bcr3360.

Abstract

Genome-wide association studies have revealed a multitude of breast cancer-associated SNPs. The majority of these SNPs are located in noncoding regions of the genome. Yet how they contribute to breast cancer development is unknown. Recently, a groundbreaking study by the Lupien group has shown that risk-associated SNPs of breast cancer are enriched for FOXA1 binding sites, which influences the function of this transcription factor.

MeSH terms

  • Binding Sites
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study*
  • Hepatocyte Nuclear Factor 3-alpha / biosynthesis
  • Hepatocyte Nuclear Factor 3-alpha / genetics*
  • Humans
  • Polymorphism, Single Nucleotide

Substances

  • FOXA1 protein, human
  • Hepatocyte Nuclear Factor 3-alpha