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C 端结合蛋白:病毒感染与肿瘤发生之间的调节剂。

C-Terminal Binding Protein: Regulator between Viral Infection and Tumorigenesis.

机构信息

Xiangya School of Medicine, Central South University, Changsha 410013, China.

Department of Microbiology, School of Basic Medical Science, Central South University, Changsha 410013, China.

出版信息

Viruses. 2024 Jun 19;16(6):988. doi: 10.3390/v16060988.

DOI:10.3390/v16060988
PMID:38932279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11209466/
Abstract

C-terminal binding protein (CtBP), a transcriptional co-repressor, significantly influences cellular signaling, impacting various biological processes including cell proliferation, differentiation, apoptosis, and immune responses. The CtBP family comprises two highly conserved proteins, CtBP1 and CtBP2, which have been shown to play critical roles in both tumorigenesis and the regulation of viral infections. Elevated CtBP expression is noted in various tumor tissues, promoting tumorigenesis, invasiveness, and metastasis through multiple pathways. Additionally, CtBP's role in viral infections varies, exhibiting differing or even opposing effects depending on the virus. This review synthesizes the advances in CtBP's function research in viral infections and virus-associated tumorigenesis, offering new insights into potential antiviral and anticancer strategies.

摘要

C 端结合蛋白(CtBP)是一种转录共抑制因子,对细胞信号转导有重要影响,涉及细胞增殖、分化、凋亡和免疫反应等多种生物学过程。CtBP 家族包括两个高度保守的蛋白 CtBP1 和 CtBP2,它们在肿瘤发生和病毒感染调控中都起着关键作用。CtBP 的表达在各种肿瘤组织中升高,通过多种途径促进肿瘤发生、侵袭和转移。此外,CtBP 在病毒感染中的作用因病毒而异,表现出不同的甚至相反的效果。本综述总结了 CtBP 在病毒感染和病毒相关肿瘤发生中的功能研究进展,为潜在的抗病毒和抗癌策略提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/11209466/0081848dded4/viruses-16-00988-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/11209466/768ffb2321a4/viruses-16-00988-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/11209466/0081848dded4/viruses-16-00988-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/11209466/768ffb2321a4/viruses-16-00988-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85e1/11209466/0081848dded4/viruses-16-00988-g002.jpg

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本文引用的文献

1
Identification and characterization of a new potent inhibitor targeting CtBP1/BARS in melanoma cells.鉴定并描述一种新型靶向黑色素瘤细胞 CtBP1/BARS 的有效抑制剂。
J Exp Clin Cancer Res. 2024 May 6;43(1):137. doi: 10.1186/s13046-024-03044-5.
2
Transcriptional corepressor activity of CtBP1 is regulated by ISG15 modification.CtBP1的转录共抑制活性受ISG15修饰调控。
Anim Cells Syst (Seoul). 2024 Feb 22;28(1):66-74. doi: 10.1080/19768354.2024.2321354. eCollection 2024.
3
Expression Analyses of C-Terminal-Binding Protein 1 (CtBP1) during Mouse Brain Development.
在小鼠脑发育过程中 C 末端结合蛋白 1(CtBP1)的表达分析。
Dev Neurosci. 2024;46(4):262-272. doi: 10.1159/000534886. Epub 2023 Oct 31.
4
C-Terminal Binding Protein 2 Emerges as a Critical Player Linking Metabolic Imbalance to the Pathogenesis of Obesity.C 端结合蛋白 2 作为连接代谢失衡与肥胖发病机制的关键因子浮出水面。
J Atheroscler Thromb. 2024 Feb 1;31(2):109-116. doi: 10.5551/jat.RV22014. Epub 2023 Oct 3.
5
Metabolic modulation of CtBP dimeric status impacts the repression of DNA damage repair genes and the platinum sensitivity of ovarian cancer.CtBP 二聚体状态的代谢调节影响 DNA 损伤修复基因的抑制和卵巢癌细胞对铂类药物的敏感性。
Int J Biol Sci. 2023 Apr 9;19(7):2081-2096. doi: 10.7150/ijbs.80952. eCollection 2023.
6
CtBP Neuroprotective Role in Toxin-Based Parkinson's Disease Models: From Expression Pattern to Dopaminergic Survival.CtBP 在基于毒素的帕金森病模型中的神经保护作用:从表达模式到多巴胺能神经元存活。
Mol Neurobiol. 2023 Aug;60(8):4246-4260. doi: 10.1007/s12035-023-03331-w. Epub 2023 Apr 15.
7
CtBP: A global regulator of balancing acts and homeostases.CtBP:平衡行为和动态平衡的全局调节剂。
Biochim Biophys Acta Rev Cancer. 2023 May;1878(3):188886. doi: 10.1016/j.bbcan.2023.188886. Epub 2023 Mar 29.
8
Epigenetic Regulation of MAP3K8 in EBV-Associated Gastric Carcinoma.EBV 相关胃癌中 MAP3K8 的表观遗传调控。
Int J Mol Sci. 2023 Jan 19;24(3):1964. doi: 10.3390/ijms24031964.
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Exp Cell Res. 2022 Dec 15;421(2):113386. doi: 10.1016/j.yexcr.2022.113386. Epub 2022 Oct 13.
10
Epstein-Barr virus: Biology and clinical disease.爱泼斯坦-巴尔病毒:生物学与临床疾病。
Cell. 2022 Sep 29;185(20):3652-3670. doi: 10.1016/j.cell.2022.08.026. Epub 2022 Sep 15.