The genetic epidemiology of breast cancer genes

J Mammary Gland Biol Neoplasia. 2004 Jul;9(3):221-36. doi: 10.1023/B:JOMG.0000048770.90334.3b.

Abstract

Genetic susceptibility to breast cancer in women is conferred by a large number of genes, of which six have so far been identified. In the context of multiple-case families, BRCA1 and BRCA2 are the most important. Mutations in these genes confer high lifetime risks of breast cancer and ovarian cancer, and more moderate risks of prostate cancer and some other cancer types. Mutations in the CHEK2 and ATM genes, by contrast, cause much more modest (2-4 fold) risks of breast cancer. Genes so far identified explain approximately 20% of the familial aggregation of breast cancer. The remaining susceptibility genes have, so far, proved illusive, suggesting that they are numerous and confer moderate risks. A variety of techniques including genome-wide association studies, use of quantitative intermediate endpoints, and resequencing of genes may be required to identify them. The identification of such genes can provide a basis for targeted prevention of breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Ataxia Telangiectasia
  • Ataxia Telangiectasia Mutated Proteins
  • Breast Neoplasms / epidemiology*
  • Breast Neoplasms / genetics*
  • Cell Cycle Proteins / genetics
  • Checkpoint Kinase 2
  • DNA-Binding Proteins / genetics
  • Female
  • Genes, BRCA1*
  • Genes, BRCA2*
  • Genetic Predisposition to Disease*
  • Humans
  • Leucine Zippers
  • Molecular Epidemiology*
  • Mutation
  • Pedigree
  • Phosphatidylinositol 3-Kinases
  • Protein Serine-Threonine Kinases / genetics
  • Risk Factors
  • Tumor Suppressor Proteins / genetics

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Tumor Suppressor Proteins
  • Checkpoint Kinase 2
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • CHEK2 protein, human
  • Protein Serine-Threonine Kinases