Martinkovich Stephen, Shah Darshan, Planey Sonia Lobo, Arnott John A
Department of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
Clin Interv Aging. 2014 Aug 28;9:1437-52. doi: 10.2147/CIA.S66690. eCollection 2014.
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.
选择性雌激素受体调节剂(SERM)是一类多样的非甾体化合物,它们以靶基因特异性和组织特异性的方式作为雌激素受体(ER)的激动剂或拮抗剂发挥作用。SERM的特异性涉及ER亚型的组织特异性表达、各种组织中共同调节蛋白的差异表达以及配体结合诱导的不同ER构象变化。迄今为止,SERM的主要临床应用是用于预防和治疗乳腺癌、预防骨质疏松症以及维持绝经后女性有益的血脂水平。然而,人们也发现SERM会引发不良反应,包括血栓栓塞事件,在某些情况下还会致癌,这些已被证明是其临床应用中的障碍。在本综述中,我们讨论了SERM组织特异性的机制,并重点介绍了知名和新兴SERM的治疗应用。