Pharmacogenomics of endocrine therapy in breast cancer

J Hum Genet. 2013 Jun;58(6):306-12. doi: 10.1038/jhg.2013.35. Epub 2013 May 2.

Abstract

The most important modality of treatment in the two-thirds of patients with an estrogen receptor (ER)-positive early breast cancer is endocrine therapy. In postmenopausal women, options include the selective ER modulators (SERMs), tamoxifen and raloxifene, and the 'third-generation' aromatase inhibitors (AIs), anastrozole, exemestane and letrozole. Under the auspices of the National Institutes of Health Global Alliance for Pharmacogenomics, Japan, the Mayo Clinic Pharmacogenomics Research Network Center and the RIKEN Center for Genomic Medicine have worked collaboratively to perform genome-wide association studies (GWAS) in women treated with both SERMs and AIs. On the basis of the results of the GWAS, scientists at the Mayo Clinic have proceeded with functional genomic laboratory studies. As will be seen in this review, this has led to new knowledge relating to endocrine biology that has provided a clear focus for further research to move toward truly personalized medicine for women with breast cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anastrozole
  • Androstadienes / therapeutic use
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Aromatase Inhibitors / therapeutic use
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Chemotherapy, Adjuvant
  • Female
  • Genome-Wide Association Study
  • Humans
  • Japan
  • Letrozole
  • Musculoskeletal Physiological Phenomena / drug effects
  • Nitriles / therapeutic use
  • Pharmacogenetics / methods*
  • Phenotype
  • Postmenopause
  • Raloxifene Hydrochloride / therapeutic use
  • Randomized Controlled Trials as Topic
  • Selective Estrogen Receptor Modulators / therapeutic use*
  • Tamoxifen / therapeutic use
  • Triazoles / therapeutic use

Substances

  • Androstadienes
  • Antineoplastic Agents, Hormonal
  • Aromatase Inhibitors
  • Nitriles
  • Selective Estrogen Receptor Modulators
  • Triazoles
  • Tamoxifen
  • Anastrozole
  • Raloxifene Hydrochloride
  • Letrozole
  • exemestane