视黄醇X受体
维甲酸
核受体
受体
生物
转录因子
癌症研究
医学
生物信息学
细胞生物学
药理学
生物化学
维甲酸
基因
作者
Mingyan Shao,Linghui Lu,Qian Qian Wang,Lin Ma,Xue Tian,Changxiang Li,Chun Li,Dongqing Guo,Qiyan Wang,Wei Wang,Yong Wang
标识
DOI:10.1016/j.biopha.2021.111264
摘要
Retinoid X receptors (RXRs) are members of ligand-dependent transcription factors whose effects on a diversity of cellular processes, including cellular proliferation, the immune response, and lipid and glucose metabolism. Knock out of RXRα causes a hypoplasia of the myocardium which is lethal during fetal life. In addition, the heart maintains a well-orchestrated balances in utilizing fatty acids (FAs) and other substrates to meet the high energy requirements. As the master transcriptional regulators of lipid metabolism, RXRs become particularly important for the energy needs of the heart. Accumulating evidence suggested that RXRs may exert direct beneficial effects in the heart both through heterodimerization with other nuclear receptors (NRs) and homodimerization, thus standing as suitable targets for treating in cardiovascular diseases. Although compounds that target RXRs are promising drugs, their use is limited by toxicity. A better understanding of the structural biology of RXRs in cardiovascular disease should enable the rational design of more selective nuclear receptor modulators to overcome these problems. Here, this review summarizes a brief overview of RXRs structure and versatility of RXR action in the control of cardiovascular diseases. And we also discussed the therapeutic potential of RXR ligand.
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