Literature DB >> 11899358

Selective estrogen receptor modulators as a new therapeutic drug group: concept to reality in a decade.

Csaba Gajdos1, V Craig Jordan.   

Abstract

This article provides an overview of the historical development, current research, clinical benefits, and potential future applications of the selective estrogen receptor modulators (SERMs), tamoxifen and raloxifene. The understanding of the mechanism of action of SERMs led not only to the development of tamoxifen, the first widely used antiestrogen for breast cancer treatment, but also to its application as a chemopreventive agent. The SERM principle of antiestrogenic actions in the breast but estrogenlike actions in bone is reviewed in clinical practice through analysis of the current applications and the potential for expanding the role of SERMs. The current view of the molecular mechanism of SERM action is summarized to identify potential target sites for future research. The clinical success of tamoxifen and raloxifene for the prevention and treatment of breast cancer and osteoporosis, respectively, has encouraged the development of a range of new agents that target breast cancer, osteoporosis, coronary heart disease, and endometrial safety.

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Year:  2002        PMID: 11899358     DOI: 10.3816/cbc.2002.n.002

Source DB:  PubMed          Journal:  Clin Breast Cancer        ISSN: 1526-8209            Impact factor:   3.225


  5 in total

1.  DT56a stimulates creatine kinase specific activity in vascular tissues of rats.

Authors:  D Somjen; I Yoles
Journal:  J Endocrinol Invest       Date:  2003-10       Impact factor: 4.256

Review 2.  Chemoprevention for pancreatic cancer.

Authors:  Robert A Wolff
Journal:  Int J Gastrointest Cancer       Date:  2003

3.  Addition of a histone deacetylase inhibitor redirects tamoxifen-treated breast cancer cells into apoptosis, which is opposed by the induction of autophagy.

Authors:  Scott Thomas; Kenneth T Thurn; Elona Biçaku; Douglas C Marchion; Pamela N Münster
Journal:  Breast Cancer Res Treat       Date:  2011-02-05       Impact factor: 4.872

4.  Efficacy and safety of DT56a compared to hormone therapy in Greek post-menopausal women.

Authors:  G Labos; E Trakakis; P Pliatsika; A Augoulea; V Vaggopoulos; G Basios; G Simeonidis; M Creatsa; A Alexandrou; Z Iliodromiti; D Kassanos; I Lambrinoudaki
Journal:  J Endocrinol Invest       Date:  2013-04-08       Impact factor: 4.256

5.  Tamoxifen-elicited uterotrophy: cross-species and cross-ligand analysis of the gene expression program.

Authors:  Joshua C Kwekel; Agnes L Forgacs; Lyle D Burgoon; Kurt J Williams; Timothy R Zacharewski
Journal:  BMC Med Genomics       Date:  2009-04-28       Impact factor: 3.063

  5 in total

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