Two decades after BRCA: Setting paradigms in personalized cancer care and prevention

Fergus J. Couch, Katherine L. Nathanson, Kenneth Offit

Research output: Contribution to journalReview article

185 Scopus citations

Abstract

The cloning of the breast cancer susceptibility genes BRCA1 and BRCA2 nearly two decades ago helped set in motion an avalanche of research exploring how genomic information can be optimally applied to identify and clinically care for individuals with a high risk of developing cancer. Genetic testing for mutations in BRCA1, BRCA2, and other breast cancer susceptibility genes has since proved to be a valuable tool for determining eligibility for enhanced screening and prevention strategies, as well as for identifying patients most likely to benefit from a targeted therapy. Here, we discuss the landscape of inherited mutations and sequence variants in BRCA1 and BRCA2, the complexities of determining disease risk when the pathogenicity of sequence variants is uncertain, and current strategies for clinical management of women who carry BRCA1/2 mutations.

Original languageEnglish (US)
Pages (from-to)1466-1470
Number of pages5
JournalScience
Volume343
Issue number6178
DOIs
StatePublished - Jan 1 2014

ASJC Scopus subject areas

  • General

Fingerprint Dive into the research topics of 'Two decades after BRCA: Setting paradigms in personalized cancer care and prevention'. Together they form a unique fingerprint.

  • Cite this