Abstract
Tamoxifen (TAM) is a selective estrogen receptor modulator that is widely used in the prevention and treatment of estrogen receptor-positive (ER +) breast cancer. Its use has significantly contributed to a decline in breast cancer mortality, since breast cancer patients treated with TAM for 5 years exhibit a 30-50% reduction in both the rate of disease recurrence after 10 years of patient follow-up and occurrence of contralateral breast cancer. However, in patients treated with TAM there is substantial interindividual variability in the development of resistance to TAM therapy, and in the incidence of TAM-induced adverse events, including deep vein thrombosis, hot flashes, and the development of endometrial cancer. This article will focus on the UDP glucuronosyltransferases, a family of metabolizing enzymes that are responsible for the deactivation and clearance of TAM and TAM metabolites, and how interindividual differences in these enzymes may play a role in patient response to TAM.
| Original language | English (US) |
|---|---|
| Title of host publication | Steroid Enzymes and Cancer |
| Publisher | Blackwell Publishing Inc. |
| Pages | 99-111 |
| Number of pages | 13 |
| ISBN (Print) | 9781573317450 |
| DOIs | |
| State | Published - Feb 2009 |
Publication series
| Name | Annals of the New York Academy of Sciences |
|---|---|
| Volume | 1155 |
| ISSN (Print) | 0077-8923 |
| ISSN (Electronic) | 1749-6632 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- General Neuroscience
- General Biochemistry, Genetics and Molecular Biology
- History and Philosophy of Science
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