过氧化物酶体增殖体激活受体:特征、功能和未来

J. Youssef, M. Badr
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引用次数: 10

摘要

本文简要回顾了过氧化物酶体增殖体激活受体(PPARα、PPARβ/δ和PPARγ)的发现历史,并介绍了它们的结构和翻译后修饰的主要特征。此外,概述了PPAR共激活剂和共抑制剂以及内源性和外源性配体。我们还总结了正在进行的重大努力,以开发更有效和更安全的PPAR调节剂,作为治疗糖尿病、癌症、动脉粥样硬化和炎症等疾病的治疗药物。最后,我们分享了一个假说,提出ppar如何控制炎症事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peroxisome Proliferator-Activated Receptors: Features, Functions, and Future
In this review, the history of the peroxisome proliferator-activated receptors (PPARα, PPARβ/δ and PPARγ) discovery is briefly traced and major features of their structure and posttranslational modifications are presented. Furthermore, an overview of PPAR coactivators and corepressors as well as of endogenous and exogenous ligands is discussed. We have also summarized significant efforts underway to develop more effective and safer PPAR modulators as therapeutic agents to treat diseases such as diabetes, cancer, atherosclerosis, and inflammation. Finally, we share a hypothesis proposing how PPARs may control inflammatory events.
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