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过氧化物酶体增殖物激活受体γ共激活因子-1α 在糖尿病心肌病中的作用机制

Peroxiredoxin Involvement in the Initiation and Progression of Human Cancer.

机构信息

1 Department of Pathology, Centre for Free Radical Research, University of Otago , Christchurch, Christchurch, New Zealand .

2 Womens Cancer Research Center, University of Pittsburgh Cancer Center , Pittsburgh, Pennsylvania.

出版信息

Antioxid Redox Signal. 2018 Mar 1;28(7):591-608. doi: 10.1089/ars.2017.7422. Epub 2018 Feb 1.

Abstract

SIGNIFICANCE

It has been proposed that cancer cells are heavily dependent on their antioxidant defenses for survival and growth. Peroxiredoxins are a family of abundant thiol-dependent peroxidases that break down hydrogen peroxide, and they have a central role in the maintenance and response of cells to alterations in redox homeostasis. As such, they are potential targets for disrupting tumor growth. Recent Advances: Genetic disruption of peroxiredoxin expression in mice leads to an increased incidence of neoplastic disease, consistent with a role for peroxiredoxins in protecting genomic integrity. In contrast, many human tumors display increased levels of peroxiredoxin expression, suggesting that strengthened antioxidant defenses provide a survival advantage for tumor progression. Peroxiredoxin inhibitors are being developed and explored as therapeutic agents in different cancer models.

CRITICAL ISSUES

It is important to complement peroxiredoxin knockout and expression studies with an improved understanding of the biological function of the peroxiredoxins. Although current results can be interpreted within the context that peroxiredoxins scavenge hydroperoxides, some peroxiredoxin family members appear to have more complex roles in regulating the response of cells to oxidative stress through protein interactions with constituents of other signaling pathways.

FUTURE DIRECTIONS

Further mechanistic information is required for understanding the role of oxidative stress in cancer, the function of peroxiredoxins in normal versus cancer cells, and for the design and testing of specific peroxiredoxin inhibitors that display selectivity to malignant cells. Antioxid. Redox Signal. 28, 591-608.

摘要

意义

有人提出,癌细胞的生存和生长严重依赖于其抗氧化防御。过氧化物酶是一类丰富的含巯基依赖的过氧化物酶,可分解过氧化氢,它们在维持细胞和响应氧化还原稳态变化方面起着核心作用。因此,它们是破坏肿瘤生长的潜在靶点。 最新进展:在小鼠中遗传破坏过氧化物酶的表达会导致肿瘤疾病的发生率增加,这与过氧化物酶在保护基因组完整性方面的作用一致。相比之下,许多人类肿瘤显示出过氧化物酶表达水平升高,表明增强的抗氧化防御为肿瘤进展提供了生存优势。过氧化物酶抑制剂正在作为不同癌症模型中的治疗剂被开发和探索。 关键问题:重要的是要通过对过氧化物酶的生物学功能有更好的理解来补充过氧化物酶敲除和表达研究。尽管目前的结果可以在过氧化物酶清除过氧化物的背景下进行解释,但一些过氧化物酶家族成员似乎通过与其他信号通路成分的蛋白质相互作用在调节细胞对氧化应激的反应方面具有更复杂的作用。 未来方向:需要进一步的机制信息来了解氧化应激在癌症中的作用、过氧化物酶在正常细胞与癌细胞中的功能,以及设计和测试对恶性细胞具有选择性的特异性过氧化物酶抑制剂。抗氧化。氧化还原信号。28,591-608。

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