The role and advance of ubiquitination and deubiquitination in depression pathogenesis and treatment

IF 3.5 4区 医学 Q2 CHEMISTRY, MEDICINAL
Xiaoru Yan, Yunhui Ma, Junting Yang, Xiaoqi Chang, Shuxuan Shi, Guohua Song
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引用次数: 0

Abstract

Depression is a common neuropsychiatric disease that is characterized by long-term, repeated low mood, pain and despair, pessimism, and even suicidal tendencies. Increasing evidence has shown that ubiquitination and deubiquitination are closely related to the occurrence of depression, including pathological morphogenesis, neuroplasticity, synaptic transmission, neuroinflammation, and so forth. The development of depression is regulated by intracellular proteins that undergo various posttranslational modifications, including ubiquitination, which falls under the epigenetics category. Although there have been studies and reviews of literature on epigenetics and depression, a systematic review of ubiquitination modification and depression has not been reported. In addition, with the deepening of research on depression and ubiquitination, the development of drugs targeting the ubiquitin system has gradually increased, but it is still not mature, so there is an urgent need to find new antidepressant drug targets. E3 ubiquitin ligases and deubiquitinating enzymes can regulate the occurrence and development of depression in a variety of ways, which may be a direction for the treatment of depression in the future. Therefore, this review describes the latest progress of ubiquitination and deubiquitination in the regulation of depression, summarizes the published signal pathways of ubiquitination and deubiquitination involved in depression, emphasizes the targets and mechanisms of E3 ubiquitin ligases and deubiquitinase in the regulation of depression, and further discusses the therapeutic targets of targeting ubiquitination modification systems to regulate depression.

泛素化和去泛素化在抑郁症发病和治疗中的作用和进展
抑郁症是一种常见的神经精神疾病,主要表现为长期反复的情绪低落、痛苦绝望、悲观厌世,甚至有自杀倾向。越来越多的证据表明,泛素化和去泛素化与抑郁症的发生密切相关,包括病理形态发生、神经可塑性、突触传递、神经炎症等。抑郁症的发生受细胞内蛋白质的调控,这些蛋白质会发生各种翻译后修饰,包括泛素化,而泛素化属于表观遗传学的范畴。虽然已有关于表观遗传学与抑郁症的研究和文献综述,但泛素化修饰与抑郁症的系统综述尚未见报道。此外,随着抑郁症与泛素化研究的深入,以泛素系统为靶点的药物开发逐渐增多,但仍不成熟,因此迫切需要寻找新的抗抑郁药物靶点。E3泛素连接酶和去泛素化酶能以多种方式调控抑郁症的发生和发展,这可能是未来治疗抑郁症的一个方向。因此,本综述介绍了泛素化和去泛素化在抑郁症调控中的最新进展,总结了已发表的涉及抑郁症的泛素化和去泛素化信号通路,强调了E3泛素连接酶和去泛素化酶在抑郁症调控中的靶点和机制,并进一步探讨了针对泛素化修饰系统调控抑郁症的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
2.60%
发文量
104
审稿时长
6-12 weeks
期刊介绍: Drug Development Research focuses on research topics related to the discovery and development of new therapeutic entities. The journal publishes original research articles on medicinal chemistry, pharmacology, biotechnology and biopharmaceuticals, toxicology, and drug delivery, formulation, and pharmacokinetics. The journal welcomes manuscripts on new compounds and technologies in all areas focused on human therapeutics, as well as global management, health care policy, and regulatory issues involving the drug discovery and development process. In addition to full-length articles, Drug Development Research publishes Brief Reports on important and timely new research findings, as well as in-depth review articles. The journal also features periodic special thematic issues devoted to specific compound classes, new technologies, and broad aspects of drug discovery and development.
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