雌激素受体- β选择性激动剂的意外科学:一类新的抗炎剂?

Nuclear receptor signaling Pub Date : 2006-01-01 Epub Date: 2006-07-07 DOI:10.1621/nrs.04012
Heather A Harris
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引用次数: 21

摘要

自从意外发现第二种雌激素受体(ER)以来的九年里,ERbeta已经在大约2800篇文献中被提及。如此多产的研究证明了人们对解释其在雌激素生理学中的作用以及研究其作为药物靶点的潜力的兴趣。我们目前的理解是erα,而不是erβ负责介导“经典”模型系统(如生殖道和骨骼)中雌激素的作用。ERbeta的作用仍在定义中,但在几种人类疾病动物模型中对ERbeta选择性激动剂的分析表明,这些化合物可能具有作为新型抗炎剂的效用。未来的挑战是阐明它们的作用机制,并确定令人印象深刻的临床前观察的临床相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The unexpected science of estrogen receptor-beta selective agonists: a new class of anti-inflammatory agents?

The unexpected science of estrogen receptor-beta selective agonists: a new class of anti-inflammatory agents?

In the nine years since the unexpected discovery of a second form of the estrogen receptor (ER), ERbeta has been mentioned in about 2,800 literature citations. Such prolific research is testimony to interest in explaining its role in estrogen physiology as well as investigating its potential as a drug target. Our current understanding is that ERalpha, not ERbeta is responsible for mediating the effects of estrogens in "classic" model systems such as the reproductive tract and skeleton. The role of ERbeta is still being defined, but profiling of ERbeta selective agonists in several animal models of human disease indicates these compounds may have utility as novel anti-inflammatory agents. The challenge for the future is to elucidate their mechanism of action and determine the clinical relevance of the impressive preclinical observations.

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