Pancholi Neha J, Price Alexander M, Weitzman Matthew D
Division of Cancer Pathobiology and Division of Protective Immunity, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Cell and Molecular Biology Graduate Program, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Philos Trans R Soc Lond B Biol Sci. 2017 Oct 19;372(1732). doi: 10.1098/rstb.2016.0269.
Viruses regulate cellular processes to facilitate viral replication. Manipulation of nuclear proteins and pathways by nuclear replicating viruses often causes cellular genome instability that contributes to transformation. The cellular DNA damage response (DDR) safeguards the host to maintain genome integrity, but DNA tumour viruses can manipulate the DDR to promote viral propagation. In this review, we describe the interactions of DNA tumour viruses with the phosphatidylinositol 3-kinase-like protein kinase (PIKK) pathways, which are central regulatory arms of the DDR. We review how signalling through the ataxia telangiectasia mutated (ATM), ataxia telangiectasia and Rad3 related (ATR), and DNA-dependent protein kinases (DNA-PK) influences viral life cycles, and how their manipulation by viral proteins may contribute to tumour formation.This article is part of the themed issue 'Human oncogenic viruses'.
病毒调节细胞过程以促进病毒复制。核复制病毒对核蛋白和信号通路的操控常常导致细胞基因组不稳定,进而促使细胞发生转化。细胞DNA损伤反应(DDR)保护宿主以维持基因组完整性,但DNA肿瘤病毒可操控DDR以促进病毒传播。在本综述中,我们描述了DNA肿瘤病毒与磷脂酰肌醇3激酶样蛋白激酶(PIKK)信号通路的相互作用,PIKK信号通路是DDR的核心调控分支。我们综述了共济失调毛细血管扩张症突变基因(ATM)、共济失调毛细血管扩张症和Rad3相关蛋白(ATR)以及DNA依赖性蛋白激酶(DNA-PK)介导的信号传导如何影响病毒生命周期,以及病毒蛋白对这些信号通路的操控如何可能导致肿瘤形成。本文是主题为“人类致癌病毒”的特刊的一部分。