Suppr超能文献

FOXO3a转录因子在肝脏氧化损伤调控中的作用

Role of FOXO3a Transcription Factor in the Regulation of Liver Oxidative Injury.

作者信息

Jin Hong, Zhang Li, He Jun, Wu Min, Jia Li, Guo Jiabin

机构信息

Center for Disease Control and Prevention of PLA, Beijing 100071, China.

School of Public Health, China Medical University, Shenyang 110122, China.

出版信息

Antioxidants (Basel). 2022 Dec 16;11(12):2478. doi: 10.3390/antiox11122478.

Abstract

Oxidative stress has been identified as a key mechanism in liver damage caused by various chemicals. The transcription factor FOXO3a has emerged as a critical regulator of redox imbalance. Multiple post-translational changes and epigenetic processes closely regulate the activity of FOXO3a, resulting in synergistic or competing impacts on its subcellular localization, stability, protein-protein interactions, DNA binding affinity, and transcriptional programs. Depending on the chemical nature and subcellular context, the oxidative-stress-mediated activation of FOXO3a can induce multiple transcriptional programs that play crucial roles in oxidative injury to the liver by chemicals. Here, we mainly review the role of FOXO3a in coordinating programs of genes that are essential for cellular homeostasis, with an emphasis on exploring the regulatory mechanisms and potential application of FOXO3a as a therapeutic target to prevent and treat liver oxidative injury.

摘要

氧化应激已被确认为各种化学物质所致肝损伤的关键机制。转录因子FOXO3a已成为氧化还原失衡的关键调节因子。多种翻译后修饰变化和表观遗传过程密切调控FOXO3a的活性,从而对其亚细胞定位、稳定性、蛋白质-蛋白质相互作用、DNA结合亲和力及转录程序产生协同或竞争性影响。根据化学物质的性质和亚细胞环境,氧化应激介导的FOXO3a激活可诱导多种转录程序,这些程序在化学物质所致的肝脏氧化损伤中起关键作用。在此,我们主要综述FOXO3a在协调细胞稳态所必需的基因程序中的作用,重点探讨FOXO3a作为预防和治疗肝脏氧化损伤治疗靶点的调控机制及潜在应用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验