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病毒规避 p53 的策略:以严重急性呼吸综合征冠状病毒为例。

Viral strategies for circumventing p53: the case of severe acute respiratory syndrome coronavirus.

机构信息

Institute for Advanced Biosciences, Inserm 1209 CNRS 5309 University Grenoble-Alpes, Grenoble, France.

出版信息

Curr Opin Oncol. 2021 Mar 1;33(2):149-158. doi: 10.1097/CCO.0000000000000713.

Abstract

PURPOSE OF REVIEW

Virtually all viruses have evolved molecular instruments to circumvent cell mechanisms that may hamper their replication, dissemination, or persistence. Among these is p53, a key gatekeeper for cell division and survival that also regulates innate immune responses. This review summarizes the strategies used by different viruses and discusses the mechanisms deployed by SARS-CoV to target p53 activities.

RECENT FINDINGS

We propose a typology for the strategies used by different viruses to address p53 functions: hit and run (e.g. IAV, ZIKV), hide and seek (e.g. HIV1), kidnap and exploit (e.g. EBV, HSV1), dominate and suppress (e.g. HR HPV). We discuss the mechanisms by which SARS nsp3 protein targets p53 for degradation and we speculate on the significance for Covid-19 pathogenesis and risk of cancer.

SUMMARY

p53 may operate as an intracellular antiviral defense mechanism. To circumvent it, SARS viruses adopt a kidnap and exploit strategy also shared by several viruses with transforming potential. This raises the question of whether SARS infections may make cells permissive to oncogenic DNA damage.

摘要

目的综述

几乎所有的病毒都进化出了分子工具,以规避可能阻碍其复制、传播或持续存在的细胞机制。其中包括 p53,它是细胞分裂和存活的关键守门员,也调节先天免疫反应。这篇综述总结了不同病毒使用的策略,并讨论了 SARS-CoV 靶向 p53 活性的机制。

最近的发现

我们提出了一种不同病毒针对 p53 功能的策略的分类法:打带跑(例如,IAV、ZIKV)、躲猫猫(例如,HIV1)、绑架和利用(例如,EBV、HSV1)、主宰和抑制(例如,HR HPV)。我们讨论了 SARS nsp3 蛋白靶向 p53 进行降解的机制,并推测了这对新冠病毒发病机制和癌症风险的意义。

总结

p53 可能作为一种细胞内抗病毒防御机制发挥作用。为了规避它,SARS 病毒采用了绑架和利用策略,这也是一些具有转化潜力的病毒所共有的策略。这就提出了一个问题,即 SARS 感染是否会使细胞对致癌性 DNA 损伤变得易受影响。

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