Estrogen receptors alpha (ERα) and beta (ERβ): subtype-selective ligands and clinical potential.

Estrogen receptors alpha (ERα) and beta (ERβ): subtype-selective ligands and clinical potential.
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DOI:
10.1016/j.steroids.2014.06.012
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发表时间:
2014-11
期刊:
影响因子:
2.7
通讯作者:
Minutolo F
Minutolo F
中科院分区:
医学3区
文献类型:
--
作者:
Paterni I;Granchi C;Katzenellenbogen JA;Minutolo F

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雌激素受体α(ERα)和β(ERβ)是核转录因子,参与调节人类许多复杂的生理过程。目前正在考虑通过预期的治疗剂调节这些受体以预防和治疗多种病理状况,例如癌症、代谢和心血管疾病、神经变性、炎症和骨质疏松症。这篇综述提供了一个概述和更新的化合物,最近已被报道为ER的调制器,特别关注其潜在的临床应用。
Estrogen receptors alpha (ERα) and beta (ERβ) are nuclear transcription factors that are involved in the regulation of many complex physiological processes in humans. Modulation of these receptors by prospective therapeutic agents is currently being considered for prevention and treatment of a wide variety of pathological conditions, such as, cancer, metabolic and cardiovascular diseases, neurodegeneration, inflammation, and osteoporosis. This review provides an overview and update of compounds that have been recently reported as modulators of ERs, with a particular focus on their potential clinical applications.
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