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Redox Status and Bioenergetics Liaison in Cancer and Neurodegeneration

机译:癌症和神经变性中的氧化还原状态和生物能联络

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摘要

During the last decades, the involvement of redox reactions in each aspect of cellular physiology has emerged, rapidly steadied, and is currently assuming extensive connotations. From a mere pathological condition leading to widespread biomolecules damage and cell degeneration, (over)production of reactive oxygen and nitrogen species (ROS and RNS, resp.) is now also deemed to be among the early upstream events of signal transduction pathways governing cellular response. It is now well established that the thiol moiety of reactive cysteines is the main molecular switch selected by the evolution to transduce a redox signal. Even at physiological pH, the sulfhydryl group of these residues is present under thiolate form and primed to be modified by ROS and RNS in a reversible manner. Snitrosylation, S-hydroxylation, and S-glutathionylation are, indeed, all oxidations that meet the conditions of specificity and reversibility required for a chemical modification (signal) being transduced in a biological event (response).
机译:在过去的几十年中,氧化还原反应参与了细胞生理学的各个方面,并迅速稳定下来,并且目前具有广泛的内涵。从导致广泛的生物分子破坏和细胞变性的单纯病理状态来看,活性氧和氮物质(ROS和RNS,分别)的(过量)产生现在也被认为是控制细胞应答的信号转导途径的早期上游事件之一。 。现在已经很好地确定,反应性半胱氨酸的硫醇部分是通过进化选择来转导氧化还原信号的主要分子开关。即使在生理pH下,这些残基的巯基也以硫醇盐形式存在,并被ROS和RNS以可逆方式修饰。实际上,亚硝基化,S-羟基化和S-谷胱甘肽化是满足生物事件(响应)中转导的化学修饰(信号)所需的特异性和可逆性条件的所有氧化。

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