Pharmacogenetics of aromatase inhibitors

Kristen D. Hadfield, William G. Newman

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Aromatase inhibitors (AIs) are an important class of endocrine drugs used in the treatment of early and advanced breast cancer in postmenopausal women. A number of studies have taken candidate approaches to assess the role of variants in genes encoding enzymes important in AI metabolism, notably CYP19A1 (aromatase), in AI response. These studies have shown conflicting, but interesting, results suggesting that CYP19A1 variants may be important in both the efficacy and toxicity of AIs. A recent genome-wide association study has identified a variant, creating an estrogen response element in TCL1A, which is associated with an increased risk of the musculoskeletal side effects associated with AI use. As breast cancer incidence increases, predictive biomarkers of response to AIs will become more important to ensure the most effective use of endocrine treatments. © 2012 Future Medicine Ltd.
    Original languageEnglish
    Pages (from-to)699-707
    Number of pages8
    JournalPharmacogenomics
    Volume13
    Issue number6
    DOIs
    Publication statusPublished - Apr 2012

    Keywords

    • aromatase inhibitors
    • breast cancer
    • pharmacogenetics
    • TCL1A

    Fingerprint

    Dive into the research topics of 'Pharmacogenetics of aromatase inhibitors'. Together they form a unique fingerprint.

    Cite this