Skinner Amy M, Turker Mitchell S
Center for Research on Occupational and Environmental Toxicology, Oregon Health & Science University, Portland, OR 97239, USA.
Sci Aging Knowledge Environ. 2005 Mar 2;2005(9):re3. doi: 10.1126/sageke.2005.9.re3.
A PubMed search for the term "oxidative stress" yields over 29,000 articles published on the subject over the past 10 years; more than 2000 of these articles also include the term "aging" in their title or abstract. Many theories of aging predict causal roles for oxidative stress in the myriad of pathological changes that occur as a function of age, including an increasing propensity to develop cancer. A possible link between aging and cancer is the induction and accumulation of somatic mutations caused by oxidative stress. This Review focuses on small mutational events that are induced by oxidative stress and the role of mismatch repair (MMR) in preventing their formation. It also discusses a possible inhibitory effect of oxidative stress on MMR. We speculate that a synergistic interaction between oxidative damage to DNA and reduced MMR levels will, in part, account for an accumulation of small mutational events, and hence cancer, with aging.
在PubMed上搜索“氧化应激”一词,可得到过去10年里发表的超过29000篇关于该主题的文章;其中2000多篇文章的标题或摘要中还包含“衰老”一词。许多衰老理论预测氧化应激在随年龄增长而发生的众多病理变化中起因果作用,包括患癌倾向增加。衰老与癌症之间的一个可能联系是氧化应激引起的体细胞突变的诱导和积累。本综述重点关注氧化应激诱导的小突变事件以及错配修复(MMR)在防止其形成中的作用。它还讨论了氧化应激对MMR可能产生的抑制作用。我们推测,DNA氧化损伤与MMR水平降低之间的协同相互作用将部分解释随着年龄增长小突变事件的积累,进而导致癌症。