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p53-p66shc-锰超氧化物歧化酶(MnSOD)网络:线粒体产生活性氧的奥秘。

The p53-p66shc-Manganese Superoxide Dismutase (MnSOD) network: a mitochondrial intrigue to generate reactive oxygen species.

作者信息

Pani Giovambattista, Koch Osvaldo Raùl, Galeotti Tommaso

机构信息

Institute of General Pathology, Catholic University Medical School, Largo F. Vito #1, 00168 Rome, Italy.

出版信息

Int J Biochem Cell Biol. 2009 May;41(5):1002-5. doi: 10.1016/j.biocel.2008.10.011. Epub 2008 Oct 18.

Abstract

Once considered as a mere by-product of respiration, mitochondrial generation of reactive oxygen species (ROS) has recently emerged as a genetically controlled phenomenon, involved in complex intracellular signal transduction cascades that directly regulate cell survival and death in responses to environmental stressors. These cascades are involved in the pathogenesis of several major age-related diseases, such as cancer and neurodegeneration, and also appear to somehow regulate the "normal" ageing process. The present short review summarizes recent discoveries on mitochondrial reactive oxygen species regulation by p53, a tumor suppressor protein and p66shc, a protein implicated in the life-span determination. It also outlines the emerging network whereby these molecules cross-talk with each other and with the mitochondrial antioxidant system, namely MnSOD (SOD2), another life-span determining protein, to regulate oxidative stress in the organelle. This molecular circuit, which comprises two genetic determinants of longevity and a major tumor suppressor gene, also provides a theoretical framework connecting senescence and cancer.

摘要

线粒体产生的活性氧(ROS)曾一度被认为只是呼吸作用的副产物,最近已成为一种受基因控制的现象,参与复杂的细胞内信号转导级联反应,该反应在应对环境应激源时直接调节细胞的存活和死亡。这些级联反应涉及几种主要的与年龄相关疾病的发病机制,如癌症和神经退行性疾病,并且似乎也以某种方式调节“正常”衰老过程。本简短综述总结了关于肿瘤抑制蛋白p53和与寿命决定相关的蛋白p66shc对线粒体活性氧调节的最新发现。它还概述了这些分子相互之间以及与线粒体抗氧化系统(即另一种与寿命决定相关的蛋白锰超氧化物歧化酶(SOD2))相互作用以调节细胞器内氧化应激的新兴网络。这个由两个长寿基因决定因素和一个主要肿瘤抑制基因组成的分子回路,也提供了一个连接衰老和癌症的理论框架。

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