Clinical pharmacology of selective estrogen receptor modulators
- PMID: 10408733
- DOI: 10.2165/00002512-199914050-00001
Clinical pharmacology of selective estrogen receptor modulators
Abstract
Observations of the pharmacology of tamoxifen and related compounds have lead to the concept of selective estrogen receptor modulators (SERMs). This new class of drug displays estrogen agonist or antagonist effects in a tissue-dependent manner and appears to offer an alternative to hormone replacement therapy for the prevention and treatment of osteoporosis and cardiovascular disease in postmenopausal women. Moreover, the estrogen antagonist actions of SERMs on breast tissue may also provide a protective effect against breast cancer. Although tamoxifen therapy reduces plasma cholesterol levels and maintains bone density, it is also associated with an increased risk of endometrial cancer, pulmonary embolism and deep vein thrombosis. This has lead to the development of newer SERMs which will hopefully lack these adverse effects of tamoxifen. These compounds promise a new era of disease prevention in the aging woman and their therapeutic potential is currently being evaluated in large-scale clinical trials.
Similar articles
-
[Estrogen receptor and selective estrogen receptor modulators (SERMs)].Nihon Rinsho. 1999 May;57(5):1199-207. Nihon Rinsho. 1999. PMID: 10361456 Review. Japanese.
-
Selective estrogen receptor modulators: a look ahead.Drugs. 1999 May;57(5):653-63. doi: 10.2165/00003495-199957050-00001. Drugs. 1999. PMID: 10353293 Review.
-
[Selective estrogen receptor modulators (SERMs) in the practice].Magy Onkol. 2002;46(2):165-75. Epub 2002 Aug 29. Magy Onkol. 2002. PMID: 12202896 Review. Hungarian.
-
Endometrial safety: a key hurdle for selective estrogen receptor modulators in development.Menopause. 2010 May-Jun;17(3):642-53. doi: 10.1097/gme.0b013e3181c4f1d6. Menopause. 2010. PMID: 20107426 Review.
-
Selective oestrogen receptor modulators/new antioestrogens: a clinical perspective.Cancer Treat Rev. 2004 Dec;30(8):695-706. doi: 10.1016/j.ctrv.2004.04.003. Cancer Treat Rev. 2004. PMID: 15541579 Review.
Cited by
-
Tamoxifen induction of Cre recombinase does not cause long-lasting or sexually divergent responses in the CNS epigenome or transcriptome: implications for the design of aging studies.Geroscience. 2019 Oct;41(5):691-708. doi: 10.1007/s11357-019-00090-2. Epub 2019 Sep 7. Geroscience. 2019. PMID: 31493147 Free PMC article.
-
Anti-osteoporosis effects of triterpenoids from the fruit of sea buckthorn (Hippophae rhamnoides) through the promotion of osteoblast differentiation in mesenchymal stem cells, C3H10T1/2.Arch Pharm Res. 2023 Oct;46(9-10):771-781. doi: 10.1007/s12272-023-01468-9. Epub 2023 Sep 26. Arch Pharm Res. 2023. PMID: 37751030
-
The Prescription Pattern of Chinese Herbal Products Containing Ginseng among Tamoxifen-Treated Female Breast Cancer Survivors in Taiwan: A Population-Based Study.Evid Based Complement Alternat Med. 2015;2015:385204. doi: 10.1155/2015/385204. Epub 2015 Mar 1. Evid Based Complement Alternat Med. 2015. PMID: 25815031 Free PMC article.
-
Estrogen-cholinergic interactions: Implications for cognitive aging.Horm Behav. 2015 Aug;74:173-85. doi: 10.1016/j.yhbeh.2015.06.022. Epub 2015 Jul 14. Horm Behav. 2015. PMID: 26187712 Free PMC article. Review.
-
Comparative tolerability of first-generation selective estrogen receptor modulators in breast cancer treatment and prevention.Drug Saf. 2001;24(14):1039-53. doi: 10.2165/00002018-200124140-00003. Drug Saf. 2001. PMID: 11735660 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources