Center for Molecular Design and Department of Pharmacology, University of Virginia Health System, 1340 Jefferson Park Avenue, Charlottesville, VA 22908, USA.
Adv Drug Deliv Rev. 2010 Oct 30;62(13):1307-15. doi: 10.1016/j.addr.2010.07.002. Epub 2010 Jul 22.
Nuclear hormone receptors comprise a superfamily of ligand-activated transcription factors that control development, differentiation, and homeostasis. Over the last 15 years a growing number of nuclear receptors have been identified that coordinate genetic networks regulating lipid metabolism and energy utilization. Several of these receptors directly sample the levels of metabolic intermediates including fatty acids and cholesterol derivatives and use this information to regulate the synthesis, transport, and breakdown of the metabolite of interest. In contrast, other family members sense metabolic activity via the presence or absence of interacting proteins. The ability of these nuclear receptors to impact metabolism will be discussed and the challenges facing drug discovery efforts for this class of targets will be highlighted.
核激素受体是配体激活转录因子的超家族,可控制发育、分化和体内平衡。在过去的 15 年中,越来越多的核受体被鉴定出来,它们协调调节脂质代谢和能量利用的遗传网络。这些受体中的一些直接检测代谢中间产物的水平,包括脂肪酸和胆固醇衍生物,并利用这些信息来调节感兴趣的代谢物的合成、运输和分解。相比之下,其他家族成员通过存在或不存在相互作用的蛋白质来感知代谢活性。本文将讨论这些核受体对代谢的影响,并强调这一类靶点的药物发现所面临的挑战。