Literature DB >> 18400579

The role of selective estrogen receptor modulators on breast cancer: from tamoxifen to raloxifene.

Wen-Ling Lee1, Ming-Huei Cheng, Hsiang-Tai Chao, Peng-Hui Wang.   

Abstract

The link between hormones and breast cancer growth and development has been recognized for more than a century. Estrogen stimulates the proliferation of breast epithelial cells, and both endogenous and exogenous estrogens have been implicated in the pathogenesis of breast cancer. Classically, estrogen action at target sites around the body is mediated through related but distinct estrogen receptors (ERs), designated ERalpha and ERbeta, to alter gene expression. This accumulating understanding of the mechanism of action of estrogen led ultimately to the design of antiestrogenic agents that work by virtue of their interaction with the ER; these drugs have come to be known as selective estrogen receptor modulators (SERMs). Tamoxifen, a SERM, emerged as the first antiestrogenic agent that is clinically applicable to breast cancer. Tamoxifen became the "gold standard" and established the principles of tumor targeting and identified the appropriate treatment strategy to aid survivorship in breast cancer patients, with enhancement of disease-free survival and a 50% decrease in recurrences observed in ER-positive patients 15 years after diagnosis. However, because of the many adverse events in the use of tamoxifen, some of which have contributed to significant morbidity and mortality, drug modification which has resulted in fewer incidences of adverse events without compromising the therapeutic effect for breast cancer prevention may face an easier road to acceptance. Raloxifene may be a better alternative, since evidence from large clinical trials showed that raloxifene not only decreases the incidence of osteoporosis and related fractures, but also offers benefits for breast cancer prevention. The results from the Study of Tamoxifen and Raloxifene (STAR) trial showed the superiority of raloxifene over tamoxifen, not only for the equal efficacy in the prevention of invasive breast cancer but also for the fewer serious adverse events. Taken together, without other competition so far, raloxifene is recommended for postmenopausal women with osteoporosis who also need breast cancer prevention.

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Year:  2008        PMID: 18400579     DOI: 10.1016/S1028-4559(08)60051-0

Source DB:  PubMed          Journal:  Taiwan J Obstet Gynecol        ISSN: 1028-4559            Impact factor:   1.705


  11 in total

Review 1.  Minireview: Lymphangioleiomyomatosis (LAM): The "Other" Steroid-Sensitive Cancer.

Authors:  Hen Prizant; Stephen R Hammes
Journal:  Endocrinology       Date:  2016-07-13       Impact factor: 4.736

2.  Indole-3-carbinol triggers aryl hydrocarbon receptor-dependent estrogen receptor (ER)alpha protein degradation in breast cancer cells disrupting an ERalpha-GATA3 transcriptional cross-regulatory loop.

Authors:  Crystal N Marconett; Shyam N Sundar; Kevin M Poindexter; Theresa R Stueve; Leonard F Bjeldanes; Gary L Firestone
Journal:  Mol Biol Cell       Date:  2010-02-03       Impact factor: 4.138

3.  Raloxifene inhibits tumor growth and lymph node metastasis in a xenograft model of metastatic mammary cancer.

Authors:  Masa-Aki Shibata; Junji Morimoto; Eiko Shibata; Hitomi Kurose; Kanako Akamatsu; Zhong-Lian Li; Moriaki Kusakabe; Masahide Ohmichi; Yoshinori Otsuki
Journal:  BMC Cancer       Date:  2010-10-19       Impact factor: 4.430

4.  Estrogen inhibits glucocorticoid action via protein phosphatase 5 (PP5)-mediated glucocorticoid receptor dephosphorylation.

Authors:  Yong Zhang; Donald Y M Leung; Steven K Nordeen; Elena Goleva
Journal:  J Biol Chem       Date:  2009-07-08       Impact factor: 5.157

5.  Novel estrogen target gene ZAS3 is overexpressed in systemic lupus erythematosus.

Authors:  Nicholas A Young; Alexandra K Friedman; Benjamin Kaffenberger; Murugesan V S Rajaram; Daniel J Birmingham; Brad H Rovin; Lee A Hebert; Larry S Schlesinger; Lai-Chu Wu; Wael N Jarjour
Journal:  Mol Immunol       Date:  2012-11-22       Impact factor: 4.407

6.  Coptis extracts enhance the anticancer effect of estrogen receptor antagonists on human breast cancer cells.

Authors:  Jing Liu; Chengwei He; Keyuan Zhou; Jingdong Wang; Jing X Kang
Journal:  Biochem Biophys Res Commun       Date:  2008-11-08       Impact factor: 3.575

Review 7.  Therapeutic options for management of endometrial hyperplasia.

Authors:  Vishal Chandra; Jong Joo Kim; Doris Mangiaracina Benbrook; Anila Dwivedi; Rajani Rai
Journal:  J Gynecol Oncol       Date:  2015-12-01       Impact factor: 4.401

8.  Secretory Endometrial Adenocarcinoma: A Rare Sequelae in a Postmenopausal Woman Following Tamoxifen Therapy for Breast Cancer.

Authors:  Sonam Sharma
Journal:  J Midlife Health       Date:  2020-09-29

9.  Nanoemulsion liquid preconcentrates for raloxifene hydrochloride: optimization and in vivo appraisal.

Authors:  Manal A Elsheikh; Yosra S R Elnaggar; Eman Y Gohar; Ossama Y Abdallah
Journal:  Int J Nanomedicine       Date:  2012-07-18

10.  Tamoxifen therapy in a murine model of myotubular myopathy.

Authors:  Nika Maani; Nesrin Sabha; Kamran Rezai; Arun Ramani; Linda Groom; Nadine Eltayeb; Faranak Mavandadnejad; Andrea Pang; Giulia Russo; Michael Brudno; Volker Haucke; Robert T Dirksen; James J Dowling
Journal:  Nat Commun       Date:  2018-11-19       Impact factor: 14.919

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