Suppr超能文献

过氧化物酶体增殖物激活受体γ激活在人非小细胞肺癌中的凋亡作用是通过脯氨酸氧化酶诱导的活性氧形成介导的。

Apoptotic action of peroxisome proliferator-activated receptor-gamma activation in human non small-cell lung cancer is mediated via proline oxidase-induced reactive oxygen species formation.

作者信息

Kim Ki Young, Ahn Jin Hee, Cheon Hyae Gyeong

机构信息

Center for Metabolic Syndrome Therapeutics, Drug Discovery Division, Korea Research Institute of Chemical Technology, Daejeon, Korea.

出版信息

Mol Pharmacol. 2007 Sep;72(3):674-85. doi: 10.1124/mol.107.035584. Epub 2007 May 29.

Abstract

Peroxisome proliferator-activated receptor (PPAR)-gamma ligands have been shown to inhibit human lung cancers by inducing apoptosis and differentiation. In the present study, we elucidated the apoptotic mechanism of PPARgamma activation in human lung cancers by using a novel PPARgamma agonist, 1-(trans-methylimino-N-oxy)-6-(2-morpholinoethoxy)-3-phenyl-(1H-indene-2-carboxylic acid ethyl ester (KR-62980), and rosiglitazone. PPARgamma activation selectively inhibited cell viability of non-small-cell lung cancer with little effect on small-cell lung cancer and normal lung cells. The cell death induced by PPARgamma activation presented apoptotic features of oligonucleosomal DNA fragmentation in A549 human non-small-cell lung cancer cell line. Reactive oxygen species (ROS) production was accompanied by increased expression of proline oxidase (POX), a redox enzyme expressed in mitochondria, upon incubation with the agonists. POX RNA interference treatment blocked PPARgamma-induced ROS formation and cytotoxicity, suggesting that POX plays a functional role in apoptosis through ROS formation. The apoptotic effects by the agonists were antagonized by bisphenol A diglycidyl ether, a PPARgamma antagonist, and by knockdown of PPARgamma expression, indicating the involvement of PPARgamma in these actions. The results of the present study suggest that PPARgamma activation induces apoptotic cell death in non-small-cell lung carcinoma mainly through ROS formation via POX induction.

摘要

过氧化物酶体增殖物激活受体(PPAR)-γ配体已被证明可通过诱导凋亡和分化来抑制人类肺癌。在本研究中,我们使用新型PPARγ激动剂1-(反式-甲基亚氨基-N-氧基)-6-(2-吗啉代乙氧基)-3-苯基-(1H-茚-2-羧酸乙酯(KR-62980)和罗格列酮,阐明了PPARγ激活在人类肺癌中的凋亡机制。PPARγ激活选择性地抑制非小细胞肺癌的细胞活力,对小细胞肺癌和正常肺细胞影响很小。PPARγ激活诱导的细胞死亡在A549人非小细胞肺癌细胞系中呈现出寡核小体DNA片段化的凋亡特征。与激动剂孵育后,活性氧(ROS)的产生伴随着脯氨酸氧化酶(POX)表达的增加,POX是一种在线粒体中表达的氧化还原酶。POX RNA干扰处理可阻断PPARγ诱导的ROS形成和细胞毒性,表明POX通过ROS形成在凋亡中发挥功能作用。激动剂的凋亡作用被PPARγ拮抗剂双酚A二缩水甘油醚和PPARγ表达的敲低所拮抗,表明PPARγ参与了这些作用。本研究结果表明,PPARγ激活主要通过诱导POX形成ROS来诱导非小细胞肺癌中的凋亡细胞死亡。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验