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关于 STAT3 与癌症氧化代谢之间相互关系的观点。

Perspectives Regarding the Intersections between STAT3 and Oxidative Metabolism in Cancer.

机构信息

College of Pharmacy, Keimyung University, Daegu 42601, Korea.

Tumor Microenvironment Global Core Research Center, College of Pharmacy, Seoul National University, Seoul 08826, Korea.

出版信息

Cells. 2020 Sep 29;9(10):2202. doi: 10.3390/cells9102202.

Abstract

Signal transducer and activator of transcription 3 (STAT3) functions as a major molecular switch that plays an important role in the communication between cytokines and kinases. In this role, it regulates the transcription of genes involved in various biochemical processes, such as proliferation, migration, and metabolism of cancer cells. STAT3 undergoes diverse post-translational modifications, such as the oxidation of cysteine by oxidative stress, the acetylation of lysine, or the phosphorylation of serine/threonine. In particular, the redox modulation of critical cysteine residues present in the DNA-binding domain of STAT3 inhibits its DNA-binding activity, resulting in the inactivation of STAT3-mediated gene expression. Accumulating evidence supports that STAT3 is a key protein that acts as a mediator of metabolism and mitochondrial activity. In this review, we focus on the post-translational modifications of STAT3 by oxidative stress and how the modification of STAT3 regulates cell metabolism, particularly in the metabolic pathways in cancer cells.

摘要

信号转导子和转录激活子 3(STAT3)作为一个主要的分子开关,在细胞因子和激酶之间的通讯中发挥着重要作用。在这个角色中,它调节参与各种生化过程的基因的转录,如癌细胞的增殖、迁移和代谢。STAT3 经历多种翻译后修饰,如氧化应激导致的半胱氨酸氧化、赖氨酸乙酰化或丝氨酸/苏氨酸磷酸化。特别是,存在于 STAT3 DNA 结合域中的关键半胱氨酸残基的氧化还原调节抑制其 DNA 结合活性,导致 STAT3 介导的基因表达失活。越来越多的证据表明,STAT3 是一种关键蛋白,作为代谢和线粒体活性的介质。在这篇综述中,我们重点介绍了氧化应激对 STAT3 的翻译后修饰以及 STAT3 的修饰如何调节细胞代谢,特别是在癌细胞中的代谢途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ddf/7600636/f6bf32c804d1/cells-09-02202-g001.jpg

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