Simulation with cells in vitro of tamoxifen treatment in premenopausal breast cancer patients with different CYP2D6 genotypes
Abstract
Tamoxifen is a prodrug that is metabolically activated by 4‐hydroxylation to the potent primary metabolite 4‐hydroxytamoxifen (4OHT) or via another primary metabolite N‐desmethyltamoxifen (NDMTAM) to a biologically active secondary metabolite endoxifen through a cytochrome P450 2D6 variant system (CYP2D6). To elucidate the mechanism of action of tamoxifen and the importance of endoxifen for its effect, we determined the anti‐oestrogenic efficacy of tamoxifen and its metabolites, including endoxifen, at concentrations corresponding to serum levels measured in breast cancer patients with various CYP2D6 genotypes (simulating tamoxifen treatment).
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Dec 01, 2014
- Source ID
- 10.1111/bph.12864
Entities
People
- Daphne J Fernandes
- David A. Flockhart
- Philipp Y. Maximov
- Puspanjali Bhatta
- Russell E Mcdaniel
- Thomas E Mürdter
- V. Craig Jordan
- Valeriy R Korostyshevskiy
Organizations
- Georgetown University
- Indiana University
- National Institutes of Health
- Susan G. Komen for the Cure
- United States Department of Defense