核受体
超家族
转录因子
计算生物学
生物
功能(生物学)
受体
药物发现
信号转导
生物信息学
神经科学
基因
药理学
细胞生物学
遗传学
作者
Thomas P. Burris,Ian Mitchelle S. de Vera,Isabelle Côté,Colin A. Flaveny,Udayanga Wanninayake,Arindam Chatterjee,John K. Walker,Nickolas Steinauer,Jinsong Zhang,Laurel A. Coons,Kenneth S. Korach,Derek W. Cain,Anthony N. Hollenberg,Paul Webb,Douglas Forrest,Anton M. Jetten,Dean P. Edwards,Sandra L. Grimm,Sean M. Hartig,Carol A. Lange
出处
期刊:Pharmacological Reviews
[American Society for Pharmacology and Experimental Therapeutics]
日期:2023-08-16
卷期号:75 (6): 1233-1318
被引量:36
标识
DOI:10.1124/pharmrev.121.000436
摘要
The nuclear receptor (NR) superfamily comprises 48 transcription factors in humans that control a plethora of gene network programs involved in a wide range of physiological processes. In this review, we will summarize and discuss recent progress in NR biology and drug development derived from the integration of various approaches, including biophysical techniques, structural studies, and translational investigations. We also highlight how defective NR signaling results in various diseases and disorders and how NRs can be targeted for therapeutic intervention via modulation via binding to synthetic lipophilic ligands. Furthermore, we also review recent studies that improved our understanding of NR structure and signaling. Significance Statement Nuclear receptors are ligand regulated transcription factors that function as key regulators of a wide range of physiological functions. NRs also serve as receptors for myriad drugs and in this review we provide an update of recent research into the function of this family of drug targets.
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