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Established Principles and Emerging Concepts on the Interplay between Mitochondrial Physiology and S-(De)nitrosylation: Implications in Cancer and Neurodegeneration.

机译:线粒体生理学与S-(去)亚硝基化之间相互作用的既定原理和新兴概念:对癌症和神经变性的影响。

摘要

S-nitrosylation is a posttranslational modification of cysteine residues that has been frequently indicated as potential molecular mechanism governing cell response upon redox unbalance downstream of nitric oxide (over)production. In the last years, increased levels of S-nitrosothiols (SNOs) have been tightly associated with the onset of nitroxidative stress-based pathologies (e.g., cancer and neurodegeneration), conditions in which alterations of mitochondrial homeostasis and activation of cellular processes dependent on it have been reported as well. In this paper we aim at summarizing the current knowledge of mitochondria-related proteins undergoing S-nitrosylation and how this redox modification might impact on mitochondrial functions, whose impairment has been correlated to tumorigenesis and neuronal cell death. In particular, emphasis will be given to the possible, but still neglected implication of denitrosylation reactions in the modulation of mitochondrial SNOs and how they can affect mitochondrion-related cellular process, such as oxidative phosphorylation, mitochondrial dynamics, and mitophagy.
机译:S-亚硝基化是半胱氨酸残基的翻译后修饰,通常被认为是潜在的分子机制,用于控制一氧化氮(过量)下游氧化还原不平衡时的细胞反应。近年来,S-亚硝基硫醇(SNOs)水平的升高与基于硝化氧化应激的病理学(例如癌症和神经退行性疾病)的发生密切相关,线粒体稳态的改变和依赖于此的细胞过程的激活也有报道。在本文中,我们旨在总结目前经历S-亚硝基化的线粒体相关蛋白的知识,以及这种氧化还原修饰如何影响线粒体功能,线粒体功能受损与肿瘤发生和神经元细胞死亡有关。特别地,将重点强调脱亚硝化反应在线粒体SNO调控中的可能意义,但仍被忽略,以及它们如何影响线粒体相关的细胞过程,例如氧化磷酸化,线粒体动力学和线粒体。

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