Peroxisome Proliferator-Activated Receptor γ and PGC-1α in Cancer: Dual Actions as Tumor Promoter and Suppressor.

IF 3.5 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
PPAR Research Pub Date : 2018-01-21 eCollection Date: 2018-01-01 DOI:10.1155/2018/6727421
Seong-Hoon Yun, Sang-Heum Han, Joo-In Park
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引用次数: 41

Abstract

Peroxisome proliferator-activated receptor γ (PPARγ) is part of a nuclear receptor superfamily that regulates gene expression involved in cell differentiation, proliferation, immune/inflammation response, and lipid metabolism. PPARγ coactivator-1α (PGC-1α), initially identified as a PPARγ-interacting protein, is an important regulator of diverse metabolic pathways, such as oxidative metabolism and energy homeostasis. The role of PGC-1α in diabetes, neurodegeneration, and cardiovascular disease is particularly well known. PGC-1α is also now known to play important roles in cancer, independent of the role of PPARγ in cancer. Though many researchers have studied the expression and clinical implications of PPARγ and PGC-1α in cancer, there are still many controversies about the role of PPARγ and PGC-1α in cancer. This review examines and summarizes some recent data on the role and action mechanisms of PPARγ and PGC-1α in cancer, respectively, particularly the recent progress in understanding the role of PPARγ in several cancers since our review was published in 2012.

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过氧化物酶体增殖物激活受体γ和PGC-1α在癌症中的双重作用:肿瘤启动子和抑制子。
过氧化物酶体增殖物激活受体γ (PPARγ)是核受体超家族的一部分,可调节参与细胞分化、增殖、免疫/炎症反应和脂质代谢的基因表达。PPARγ共激活因子-1α (PGC-1α)最初被确定为PPARγ相互作用蛋白,是多种代谢途径的重要调节因子,如氧化代谢和能量稳态。PGC-1α在糖尿病、神经变性和心血管疾病中的作用是众所周知的。PGC-1α现在也被认为在癌症中发挥重要作用,独立于PPARγ在癌症中的作用。尽管许多研究者研究了PPARγ和PGC-1α在癌症中的表达及其临床意义,但关于PPARγ和PGC-1α在癌症中的作用仍存在许多争议。本文回顾和总结了PPARγ和PGC-1α在癌症中的作用和作用机制,特别是自2012年我们的综述发表以来,对PPARγ在几种癌症中的作用的最新研究进展。
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来源期刊
PPAR Research
PPAR Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.20
自引率
3.40%
发文量
17
审稿时长
12 months
期刊介绍: PPAR Research is a peer-reviewed, Open Access journal that publishes original research and review articles on advances in basic research focusing on mechanisms involved in the activation of peroxisome proliferator-activated receptors (PPARs), as well as their role in the regulation of cellular differentiation, development, energy homeostasis and metabolic function. The journal also welcomes preclinical and clinical trials of drugs that can modulate PPAR activity, with a view to treating chronic diseases and disorders such as dyslipidemia, diabetes, adipocyte differentiation, inflammation, cancer, lung diseases, neurodegenerative disorders, and obesity.
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