核受体
受体
过氧化物酶体增殖物激活受体
PPAR激动剂
炎症
兴奋剂
药理学
转录因子
化学
部分激动剂
脂质代谢
癌症研究
内科学
医学
生物化学
基因
作者
Agha Zeeshan Mirza,Ismail Althagafi,Hina Shamshad
标识
DOI:10.1016/j.ejmech.2019.01.067
摘要
The peroxisome proliferator-activated receptors (PPAR-α, PPAR-β/δ, and PPAR-γ) are members of the nuclear receptor super-family, acting as ligand-inducible transcription factors and play crucial roles in glucose and lipid metabolism. These are a well-known receptor for diabetic therapy, not only influence the cardiovascular systems but are also expressed in many human solid tumors. For atherosclerosis, inflammation, and hypertension, the PPARs are considered as important therapeutic targets. Furthermore, it has been suggested that careful designing of partial agonists for PPARs, may show improvement with the side effects and also increase the therapeutic value for different diseases as cancer, inflammation and cardiovascular etc. This review summaries structural features of PPAR receptors, illustrates the method of PPAR modulator design, then analyzes recent dual- and pan-agonist with different therapeutic outcomes of the receptor to be used as a target for drugs in future. The advances in PPARs antagonists, their classification and structure-activity relationship are also summarized.
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