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逃离死亡:癌细胞中的线粒体氧化还原稳态

Escaping Death: Mitochondrial Redox Homeostasis in Cancer Cells.

作者信息

Ciccarese Francesco, Ciminale Vincenzo

机构信息

Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.

Veneto Institute of Oncology - IRCCS, Padua, Italy.

出版信息

Front Oncol. 2017 Jun 9;7:117. doi: 10.3389/fonc.2017.00117. eCollection 2017.

Abstract

Reactive oxygen species (ROS) are important signaling molecules that act through the oxidation of nucleic acids, proteins, and lipids. Several hallmarks of cancer, including uncontrolled proliferation, angiogenesis, and genomic instability, are promoted by the increased ROS levels commonly found in tumor cells. To counteract excessive ROS accumulation, oxidative stress, and death, cancer cells tightly regulate ROS levels by enhancing scavenging enzymes, which are dependent on the reducing cofactor nicotinamide adenine dinucleotide phosphate (NADPH). This review focuses on mitochondrial ROS homeostasis with a description of six pathways of NADPH production in mitochondria and a discussion of the possible strategies of pharmacological intervention to selectively eliminate cancer cells by increasing their ROS levels.

摘要

活性氧(ROS)是重要的信号分子,通过氧化核酸、蛋白质和脂质发挥作用。肿瘤细胞中常见的ROS水平升高会促进癌症的几个特征,包括不受控制的增殖、血管生成和基因组不稳定。为了对抗过量的ROS积累、氧化应激和细胞死亡,癌细胞通过增强清除酶来严格调节ROS水平,这些酶依赖于还原性辅因子烟酰胺腺嘌呤二核苷酸磷酸(NADPH)。本综述重点关注线粒体ROS稳态,描述线粒体中NADPH产生的六种途径,并讨论通过提高癌细胞ROS水平来选择性消除癌细胞的可能药物干预策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bc/5465272/36f4938df7d6/fonc-07-00117-g001.jpg

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