Literature DB >> 8796891

Targeted anti-estrogens to treat and prevent diseases in women.

D A Tonetti1, V C Jordan.   

Abstract

The estrogen receptor has been successfully targeted with the anti-estrogen tamoxifen to treat all stages of breast cancer. Because tamoxifen is a partial agonist, it exhibits target-site specificity: it acts as an anti-estrogen in the breast to inhibit tumor growth, while exhibiting estrogenic effects on bones and lipid metabolism. Therefore, tamoxifen has the added benefit of maintaining bone density and reducing the risk of myocardial infarction in postmenopausal women. However, undesirable side effects of tamoxifen preclude its use as a hormone replacement therapy for otherwise healthy women. New anti-estrogens are currently being developed that may prevent osteoporosis, breast and endometrial cancer, and reduce the risk of myocardial infarction.

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Year:  1996        PMID: 8796891     DOI: 10.1016/1357-4310(96)88775-2

Source DB:  PubMed          Journal:  Mol Med Today        ISSN: 1357-4310


  4 in total

1.  Different positioning of the ligand-binding domain helix 12 and the F domain of the estrogen receptor accounts for functional differences between agonists and antagonists.

Authors:  M Nichols; J M Rientjes; A F Stewart
Journal:  EMBO J       Date:  1998-02-02       Impact factor: 11.598

2.  Tamoxifen inhibits acidification in cells independent of the estrogen receptor.

Authors:  N Altan; Y Chen; M Schindler; S M Simon
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-13       Impact factor: 11.205

3.  Role of SUMOylation in full antiestrogenicity.

Authors:  Khalid Hilmi; Nader Hussein; Rodrigo Mendoza-Sanchez; Mohamed El-Ezzy; Houssam Ismail; Chantal Durette; Martine Bail; Maria Johanna Rozendaal; Michel Bouvier; Pierre Thibault; James L Gleason; Sylvie Mader
Journal:  Mol Cell Biol       Date:  2012-07-23       Impact factor: 4.272

4.  Differential effects of selective oestrogen receptor modulators (SERMs) tamoxifen, ospemifene and raloxifene on human osteoclasts in vitro.

Authors:  H Michael; P L Härkönen; L Kangas; H K Väänänen; T A Hentunen
Journal:  Br J Pharmacol       Date:  2007-04-10       Impact factor: 8.739

  4 in total

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