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致癌过程中的氧化应激与氧化损伤

Oxidative stress and oxidative damage in carcinogenesis.

作者信息

Klaunig James E, Kamendulis Lisa M, Hocevar Barbara A

机构信息

Indiana University School of Medicine, Indianapolis, IN 46202, USA.

出版信息

Toxicol Pathol. 2010 Jan;38(1):96-109. doi: 10.1177/0192623309356453. Epub 2009 Dec 17.

Abstract

Carcinogenesis is a multistep process involving mutation and the subsequent selective clonal expansion of the mutated cell. Chemical and physical agents including those that induce reative oxygen species can induce and/or modulate this multistep process. Several modes of action by which carcinogens induce cancer have been identified, including through production of reactive oxygen species (ROS). Oxidative damage to cellular macromolecules can arise through overproduction of ROS and faulty antioxidant and/or DNA repair mechanisms. In addition, ROS can stimulate signal transduction pathways and lead to activation of key transcription factors such as Nrf2 and NF-kappaB. The resultant altered gene expression patterns evoked by ROS contribute to the carcinogenesis process. Recent evidence demonstrates an association between a number of single nucleotide polymorphisms (SNPs) in oxidative DNA repair genes and antioxidant genes with human cancer susceptibility. These aspects of ROS biology will be discussed in the context of their relationship to carcinogenesis.

摘要

致癌作用是一个多步骤过程,涉及突变以及随后突变细胞的选择性克隆扩增。化学和物理因素,包括那些诱导活性氧的因素,能够诱导和/或调节这一多步骤过程。已经确定了致癌物诱发癌症的几种作用方式,包括通过产生活性氧(ROS)。细胞大分子的氧化损伤可通过活性氧的过量产生以及有缺陷的抗氧化剂和/或DNA修复机制而出现。此外,活性氧可刺激信号转导通路,并导致关键转录因子如Nrf2和核因子κB的激活。活性氧引起的基因表达模式改变有助于致癌过程。最近的证据表明,氧化DNA修复基因和抗氧化剂基因中的一些单核苷酸多态性(SNP)与人类癌症易感性之间存在关联。活性氧生物学的这些方面将在它们与致癌作用的关系背景下进行讨论。

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