Tamoxifen: Difference between revisions
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In [[medicine]], '''tamoxifen''' is "one of the [[selective estrogen receptor modulator]]s with tissue-specific activities. Tamoxifen acts as an anti-[[estrogen]] (inhibiting agent) in the mammary tissue, but as an estrogen (stimulating agent) in [[cholesterol]] metabolism, [[bone mineral density|bone density]], and cell proliferation in the [[endometrium]]. | In [[medicine]], '''tamoxifen''' is "one of the [[selective estrogen receptor modulator]]s with tissue-specific activities. Tamoxifen acts as an anti-[[estrogen]] (inhibiting agent) in the mammary tissue, but as an estrogen (stimulating agent) in [[cholesterol]] metabolism, [[bone mineral density|bone density]], and cell proliferation in the [[endometrium]]. | ||
Until the introduction of the [[aromatase inhibitor]]s, tamoxifen was the gold standard for chemotherapy of [[breast cancer]], and remains important in its treatment, especially of premenopausal women. It is also used to treat other hormonally sensitive cancers, such as [[melanoma]]. | |||
==Pharmacology== | ==Pharmacology== | ||
===Administration=== | ===Administration=== | ||
Latest revision as of 18:00, 2 July 2010
In medicine, tamoxifen is "one of the selective estrogen receptor modulators with tissue-specific activities. Tamoxifen acts as an anti-estrogen (inhibiting agent) in the mammary tissue, but as an estrogen (stimulating agent) in cholesterol metabolism, bone density, and cell proliferation in the endometrium.
Until the introduction of the aromatase inhibitors, tamoxifen was the gold standard for chemotherapy of breast cancer, and remains important in its treatment, especially of premenopausal women. It is also used to treat other hormonally sensitive cancers, such as melanoma.
Pharmacology
Administration
Distribution
Metabolism
Tamoxifen is metabolized in the liver by cytochrome P-450 CYP2D6 to active metabolites.
Excretion
Toxicity
Drug interactions
Paroxetine may increase death from breast cancer among women taking tamoxifen due to inhibiting metabolism of tamoxifen to its active metabolite by cytochrome P-450 CYP2D6.[1]
References
- ↑ Kelly, Catherine M; David N Juurlink, Tara Gomes, Minh Duong-Hua, Kathleen I Pritchard, Peter C Austin, Lawrence F Paszat (2010-02-08). "Selective serotonin reuptake inhibitors and breast cancer mortality in women receiving tamoxifen: a population based cohort study". BMJ 340 (feb08_1): c693. DOI:10.1136/bmj.c693. Retrieved on 2010-02-10. Research Blogging.