Otto-Warburg Laboratory, Max Planck Institute for Molecular Genetics, Ihnestrasse 73, 14195 Berlin, Germany; University of Würzburg, CU Systems Medicine, Josef-Schneider-Straße 2, Building D15, 97070 Wuerzburg, Germany.
Trends Pharmacol Sci. 2015 Oct;36(10):688-704. doi: 10.1016/j.tips.2015.06.010.
Nuclear receptors are ligand-activated transcription factors, which represent a primary class of drug targets. The nuclear receptor peroxisome proliferator-activated receptor gamma (PPARγ) is a key player in various biological processes. PPARγ is widely known as the target protein of the thiazolidinediones for treating type 2 diabetes. Moreover, PPARγ ligands can induce anti-inflammatory and potentially additional beneficial effects. Recent mechanistic insights of PPARγ modulation give hope the next generation of efficient PPARγ-based drugs with fewer side effects can be developed. Furthermore, chemical approaches that make use of synergistic action of combinatorial ligands are promising alternatives for providing tailored medicine. Lessons learned from fine-tuning the action of PPARγ can provide avenues for efficient molecular intervention via many other nuclear receptors to combat common diseases.
核受体是配体激活的转录因子,是药物靶点的主要类别之一。核受体过氧化物酶体增殖物激活受体γ(PPARγ)是各种生物过程中的关键因子。PPARγ 是众所周知的噻唑烷二酮类药物治疗 2 型糖尿病的靶蛋白。此外,PPARγ 配体可诱导抗炎和潜在的其他有益作用。对 PPARγ 调节的最新机制研究表明,希望能够开发出具有更少副作用的下一代高效基于 PPARγ 的药物。此外,利用组合配体协同作用的化学方法为提供定制药物提供了有前途的替代方法。从微调 PPARγ 作用中获得的经验教训可以为通过许多其他核受体进行有效的分子干预提供途径,以对抗常见疾病。