Selective estrogen receptor modulators: tissue specificity and clinical utility

被引:191
作者
Martinkovich, Stephen [1 ]
Shah, Darshan [1 ]
Planey, Sonia Lobo [1 ]
Arnott, John A. [1 ]
机构
[1] Commonwealth Med Coll, Dept Basic Sci, Scranton, PA 18509 USA
关键词
selective estrogen receptor modulators; SERMs; estrogen receptors; TAMOXIFEN-DNA ADDUCTS; PREVENTS BONE LOSS; STEROID-HORMONE RECEPTORS; SURGICAL ADJUVANT BREAST; VERTEBRAL FRACTURE RISK; POSTMENOPAUSAL WOMEN; PHASE-II; BAZEDOXIFENE ACETATE; ENDOMETRIAL CANCER; DOUBLE-BLIND;
D O I
10.2147/CIA.S66690
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Selective estrogen receptor modulators (SERMs) are a diverse group of nonsteroidal compounds that function as agonists or antagonists for estrogen receptors (ERs) in a target gene-specific and tissue-specific fashion. SERM specificity involves tissue-specific expression of ER subtypes, differential expression of co-regulatory proteins in various tissues, and varying ER conformational changes induced by ligand binding. To date, the major clinical applications of SERMs are their use in the prevention and treatment of breast cancer, the prevention of osteoporosis, and the maintenance of beneficial serum lipid profiles in postmenopausal women. However, SERMs have also been found to promote adverse effects, including thromboembolic events and, in some cases, carcinogenesis, that have proven to be obstacles in their clinical utility. In this review, we discuss the mechanisms of SERM tissue specificity and highlight the therapeutic application of well-known and emergent SERMs.
引用
收藏
页码:1437 / 1452
页数:16
相关论文
共 200 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]   Urogenital effects of selective estrogen receptor modulators: a systematic review [J].
Albertazzi, P ;
Sharma, S .
CLIMACTERIC, 2005, 8 (03) :214-220
[3]  
[Anonymous], 1988, NEW ENGL J MED, V319, P1681
[4]   The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site [J].
Anstead, GM ;
Carlson, KE ;
Katzenellenbogen, JA .
STEROIDS, 1997, 62 (03) :268-303
[5]   Bazedoxifene, a selective estrogen receptor modulator: effects on the endometrium, ovaries, and breast from a randomized controlled trial in osteoporotic postmenopausal women [J].
Archer, David F. ;
Pinkerton, JoAnn V. ;
Utian, Wulf H. ;
Menegoci, Jose C. ;
de Villiers, Tobie J. ;
Yuen, Chui Kin ;
Levine, Amy B. ;
Chines, Arkadi A. ;
Constantine, Ginger D. .
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2009, 16 (06) :1109-1115
[6]   Lessons from the dissection of the activation functions (AF-1 and AF-2) of the estrogen receptor alpha in vivo [J].
Arnal, Jean-Francois ;
Fontaine, Coralie ;
Abot, Anne ;
Valera, Marie-Cecile ;
Laurell, Henrik ;
Gourdy, Pierre ;
Lenfant, Francoise .
STEROIDS, 2013, 78 (06) :576-582
[7]   Idoxifene versus tamoxifen: a randomized comparison in postmenopausal. patients with metastatic breast cancer [J].
Arpino, G ;
Krishnan, MN ;
Dinesh, CD ;
Bardou, VJ ;
Clark, GM ;
Elledge, RM .
ANNALS OF ONCOLOGY, 2003, 14 (02) :233-241
[8]  
Ascenzi Paolo, 2006, Molecular Aspects of Medicine, V27, P299, DOI 10.1016/j.mam.2006.07.001
[9]   Randomized, double-blind, multicenter trial comparing two doses of arzoxifene (LY353381) in hormone-sensitive advanced or metastatic breast cancer patients [J].
Baselga, J ;
Llombart-Cussac, A ;
Bellet, M ;
Guillem-Porta, V ;
Enas, N ;
Krejcy, K ;
Carrasco, E ;
Kayitalire, L ;
Kuta, M ;
Lluch, A ;
Vodvarka, P ;
Kerbrat, P ;
Namer, M ;
Petruzelka, L .
ANNALS OF ONCOLOGY, 2003, 14 (09) :1383-1390
[10]   STEROID-HORMONE RECEPTORS - MANY ACTORS IN SEARCH OF A PLOT [J].
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G .
CELL, 1995, 83 (06) :851-857