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The Ying-Yang of the virus-host interaction: control of the DNA damage response.

机译:病毒与宿主相互作用的颖杨:控制DNA损伤反应。

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Evaluation of: Nikitin PA, Yan CM, Forte E et al.: An ATM/Chk2-mediated DNA damage-responsive signaling pathway suppresses Epstein-Barr virus transformation of primary human B cells. Cell. Host Microbe 8(6), 510-522 (2010). Viruses have evolved elegant strategies to manipulate the host while the host counters with defense systems including the interferon response, apoptosis and the DNA damage response (DDR). Viruses have multiple strategies for manipulating the DDR and the same virus can even activate or inhibit the DDR at different stages of infection. Epstein-Barr virus (EBV) is implicated in several human cancers, including Burkitt's lymphoma, nasopharyngeal carcinoma, post-transplant lymphoproliferative disease and HIV-associated lymphomas. Although multiple viral proteins have been implicated in EBV-associated malignancies, the cellular pathways that control EBV-induced transformation and tumorigenesis remain incompletely understood. In this study, Nikitin et al. demonstrate that early EBV infection induces a cellular DDR that restricts virus-mediated transformation. The EBV-encoded EBNA3C protein subsequently attenuates this response to favor transformation and immortalization of host cells.
机译:评价:Nikitin PA,Yan CM,Forte E等:ATM / Chk2介导的DNA损伤应答信号通路抑制了原代人B细胞的爱泼斯坦-巴尔病毒转化。细胞。宿主微生物8(6),510-522(2010)。病毒已经进化出巧妙的策略来操纵宿主,而宿主会对抗防御系统,包括干扰素反应,凋亡和DNA损伤反应(DDR)。病毒具有操纵DDR的多种策略,同一病毒甚至可以在感染的不同阶段激活或抑制DDR。爱泼斯坦-巴尔病毒(EBV)与几种人类癌症有关,包括伯基特氏淋巴瘤,鼻咽癌,移植后淋巴增生性疾病和与HIV相关的淋巴瘤。尽管多种病毒蛋白已被证明与EBV相关的恶性肿瘤有关,但控制EBV诱导的转化和肿瘤发生的细胞途径仍未完全了解。在这项研究中,Nikitin等人。证明早期EBV感染会诱导细胞DDR,从而限制病毒介导的转化。 EBV编码的EBNA3C蛋白随后减弱了这种应答,从而有利于宿主细胞的转化和永生化。

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