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孤儿核受体:将内分泌学逆向转变

Orphan nuclear receptors: shifting endocrinology into reverse.

作者信息

Kliewer S A, Lehmann J M, Willson T M

机构信息

Department of Molecular Endocrinology, Glaxo Wellcome Research and Development, Five Moore Drive, Research Triangle Park, NC 27709, USA.

出版信息

Science. 1999 Apr 30;284(5415):757-60. doi: 10.1126/science.284.5415.757.

Abstract

Steroid and thyroid hormones and vitamin A metabolites (retinoids) regulate the expression of complex gene programs by binding to members of the nuclear receptor family of ligand-activated transcription factors. The nuclear receptor family also includes many "orphan" members that currently lack known ligands but that represent candidate receptors for new hormones. Recently, natural and synthetic ligands have been identified for several orphan receptors and used to dissect their biological roles. This "reverse endocrinology" strategy has resulted in the discovery of unanticipated nuclear signaling pathways for retinoids, fatty acids, eicosanoids, and steroids with important physiological and pharmacological ramifications.

摘要

类固醇、甲状腺激素和维生素A代谢产物(类视黄醇)通过与配体激活转录因子的核受体家族成员结合来调节复杂基因程序的表达。核受体家族还包括许多“孤儿”成员,它们目前缺乏已知的配体,但代表了新激素的候选受体。最近,已为几种孤儿受体鉴定出天然和合成配体,并用于剖析它们的生物学作用。这种“逆向内分泌学”策略导致发现了类视黄醇、脂肪酸、类二十烷酸和类固醇的意外核信号通路,具有重要的生理和药理学意义。

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