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线粒体过氧化物酶体增殖物激活受体3(硫氧还蛋白过氧化物酶2)表达增加可保护癌细胞免受缺氧和药物诱导的过氧化氢依赖性凋亡。

Increased expression of mitochondrial peroxiredoxin-3 (thioredoxin peroxidase-2) protects cancer cells against hypoxia and drug-induced hydrogen peroxide-dependent apoptosis.

作者信息

Nonn Larisa, Berggren Margareta, Powis Garth

机构信息

Arizona Cancer Center, University of Arizona, Tucson, AZ 85724-5024, USA.

出版信息

Mol Cancer Res. 2003 Jul;1(9):682-9.

Abstract

Peroxiredoxin-3 (Prdx3) is a mitochondrial member of the antioxidant family of thioredoxin peroxidases that uses mitochondrial thioredoxin-2 (Trx2) as a source of reducing equivalents to scavenge hydrogen peroxide (H(2)O(2)). Low levels of H(2)O(2) produced by the mitochondria regulate physiological processes, including cell proliferation, while high levels of H(2)O(2) are toxic to the cell and cause apoptosis. WEHI7.2 thymoma cells with stable overexpression of Prdx3 displayed decreased levels of cellular H(2)O(2) and decreased cell proliferation without a change in basal levels of apoptosis. Prdx3-transfected cells showed a marked resistance to hypoxia-induced H(2)O(2) formation and apoptosis. Prdx3 overexpression also protected the cells against apoptosis caused by H(2)O(2), t-butylhydroperoxide, and the anticancer drug imexon, but not by dexamethasone. Thus, mitochondrial Prdx3 is an important cellular antioxidant that regulates physiological levels of H(2)O(2), leading to decreased cell growth while protecting cells from the apoptosis-inducing effects of high levels of H(2)O(2).

摘要

过氧化物酶-3(Prdx3)是硫氧还蛋白过氧化物酶抗氧化家族的线粒体成员,它利用线粒体硫氧还蛋白-2(Trx2)作为还原当量的来源来清除过氧化氢(H₂O₂)。线粒体产生的低水平H₂O₂调节包括细胞增殖在内的生理过程,而高水平的H₂O₂对细胞有毒并导致细胞凋亡。稳定过表达Prdx3的WEHI7.2胸腺瘤细胞显示细胞内H₂O₂水平降低且细胞增殖减少,而基础凋亡水平无变化。Prdx3转染的细胞对缺氧诱导的H₂O₂形成和凋亡表现出明显抗性。Prdx3过表达还保护细胞免受H₂O₂、叔丁基过氧化氢和抗癌药物艾美克生引起的凋亡,但地塞米松引起的凋亡除外。因此,线粒体Prdx3是一种重要的细胞抗氧化剂,它调节H₂O₂的生理水平,导致细胞生长减少,同时保护细胞免受高水平H₂O₂诱导凋亡的影响。

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