Kulak Júnior Jaime, Kulak Carolina Aguiar Moreira, Taylor Hugh S
Hospital de Clínicas, Universidade Federal do Paraná, Curitiba, PR, Brasil.
Arq Bras Endocrinol Metabol. 2010 Mar;54(2):200-5. doi: 10.1590/s0004-27302010000200016.
Selective estrogen receptor modulators (SERMs) have the ability to bind the estrogen receptor (ER) and are known to confer ER agonist or antagonist effects depending on the target tissue. A number of newer SERMs, including bazedoxifene, lasofoxifene and ospemifene, are currently under clinical development for the prevention and treatment of postmenopausal osteoporosis and for other indications. Although the possibility of developing a single agent that has all of the desired characteristics of an ideal SERM seems to be unlikely, progress in the clinical development of SERMs targeted to the ER suggests that these newer compounds may have attributes that represent an improvement relative to existing SERMs. A new approach to menopausal therapy is the tissue selective estrogen complex or the pairing of a selective estrogen receptor modulator with estrogens. Further investigation will help to clarify relative benefits/risks of novel SERMs in development within specific indications.
选择性雌激素受体调节剂(SERMs)能够与雌激素受体(ER)结合,并且已知根据靶组织的不同会产生ER激动剂或拮抗剂效应。包括巴多昔芬、拉索昔芬和奥昔芬在内的一些新型SERMs目前正处于临床开发阶段,用于预防和治疗绝经后骨质疏松症以及其他适应症。尽管开发一种具有理想SERMs所有期望特性的单一药物似乎不太可能,但针对ER的SERMs临床开发进展表明,这些新型化合物可能具有相对于现有SERMs有所改进的特性。绝经治疗的一种新方法是组织选择性雌激素复合物或选择性雌激素受体调节剂与雌激素的联合使用。进一步的研究将有助于阐明正在开发的新型SERMs在特定适应症中的相对获益/风险。