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氧化还原平衡:对抗癌症恶病质中肌肉消耗的干预靶点?

The Redox Balance: A Target for Interventions Against Muscle Wasting in Cancer Cachexia?

作者信息

Penna Fabio, Ballarò Riccardo, Costelli Paola

机构信息

Department of Clinical and Biological Sciences, University of Torino, Torino, Italy.

出版信息

Antioxid Redox Signal. 2020 Sep 10;33(8):542-558. doi: 10.1089/ars.2020.8041. Epub 2020 Mar 5.

Abstract

The management of cancer patients is frequently complicated by the occurrence of a complex syndrome known as cachexia. It is mainly characterized by muscle wasting, a condition that associates with enhanced protein breakdown and with negative energy balance. While the mechanisms underlying cachexia have been only partially elucidated, understanding the pathogenesis of muscle wasting in cancer hosts is mandatory to design new targeted therapeutic strategies. Indeed, most of cancer patients will experience cachexia during the course of their disease, and about 25% of cancer-related deaths are due to this syndrome, rather than to the tumor itself. Compelling evidence suggests that an altered redox homeostasis likely contributes to cancer-induced muscle protein depletion, directly or indirectly activating the intracellular degradative pathways. In addition, oxidative stress impinges on both mitochondrial number and function; the other way round, altered mitochondria lead to enhanced redox imbalance, creating a vicious loop that eventually results in negative energy metabolism. The present review focuses on the possibility that pharmacological and nonpharmacological strategies able to restore a physiologic redox balance could be useful components of treatment schedules aimed at counteracting cancer-induced muscle wasting. Exercise and the use of exercise mimetic drugs represent the most promising approaches capable of reinforcing the muscle antioxidant defenses of cancer patients. The results from ongoing and new clinical trials are needed to validate the preclinical studies and provide effective therapies for cancer cachexia. . 33, 542-558.

摘要

癌症患者的管理常常因一种名为恶病质的复杂综合征的出现而变得复杂。它主要特征为肌肉消耗,这种情况与蛋白质分解增强以及负能量平衡相关。虽然恶病质的潜在机制仅得到部分阐明,但了解癌症宿主中肌肉消耗的发病机制对于设计新的靶向治疗策略至关重要。事实上,大多数癌症患者在疾病过程中会经历恶病质,约25%的癌症相关死亡归因于该综合征,而非肿瘤本身。有力证据表明,氧化还原稳态的改变可能直接或间接激活细胞内降解途径,从而导致癌症诱导的肌肉蛋白质消耗。此外,氧化应激影响线粒体数量和功能;反之,线粒体改变导致氧化还原失衡加剧,形成恶性循环,最终导致负能量代谢。本综述聚焦于这样一种可能性,即能够恢复生理氧化还原平衡的药理学和非药理学策略可能是旨在对抗癌症诱导的肌肉消耗的治疗方案的有用组成部分。运动以及使用运动模拟药物是最有希望增强癌症患者肌肉抗氧化防御的方法。需要正在进行的和新的临床试验结果来验证临床前研究,并为癌症恶病质提供有效的治疗方法。. 33, 542 - 558。

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