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[基于PPARγ靶点基因组的药物发现:现状与未来方向]

[PPARgamma targeted genome-based drug discovery; present and future direction].

作者信息

Miyachi Hiroyuki

机构信息

Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University.

出版信息

Nihon Rinsho. 2010 Feb;68(2):243-8.

Abstract

Peroxisome proliferator-activated receptor gamma (PPARgamma) is known to regulate growth arrest and terminal differentiation of adipocytes initially, and glitazones are used as a new class of antidiabetic drugs clinically. Recent understanding of the functions of PPARs, using genome-wide analysis, as pleiotropic regulators of biological responses, including not only lipid, lipoprotein, glucose homeostasis, but also inflammation, differentiation and proliferation of various cancer cells, and memory, have provided an opportunity to develop novel PPARs ligands with characteristic subtype selectivity. Such ligands are not only chemical tools to investigate the functions of PPARs, but also candidates for the treatment of PPARs-mediated diseases. This article summarizes recent topics of the medicinal chemistry work on the design, synthesis and pharmacological evaluation of PPARs related agents.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)最初被认为可调节脂肪细胞的生长停滞和终末分化,而格列酮类药物在临床上被用作一类新型抗糖尿病药物。最近,通过全基因组分析对PPARs功能的认识表明,PPARs作为生物反应的多效性调节因子,不仅涉及脂质、脂蛋白、葡萄糖稳态,还包括各种癌细胞的炎症、分化和增殖以及记忆等方面,这为开发具有特征性亚型选择性的新型PPARs配体提供了契机。此类配体不仅是研究PPARs功能的化学工具,也是治疗PPARs介导疾病的候选药物。本文总结了PPARs相关药物的设计、合成及药理评价方面药物化学研究的最新进展。

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