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在腺病毒感染期间使细胞内抗病毒反应失活。

Inactivating intracellular antiviral responses during adenovirus infection.

作者信息

Weitzman Matthew D, Ornelles David A

机构信息

Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA 92037, USA.

出版信息

Oncogene. 2005 Nov 21;24(52):7686-96. doi: 10.1038/sj.onc.1209063.

Abstract

DNA viruses promote cell cycle progression, stimulate unscheduled DNA synthesis, and present the cell with an extraordinary amount of exogenous DNA. These insults elicit vigorous responses mediated by cellular factors that govern cellular homeostasis. To ensure productive infection, adenovirus has developed means to inactivate these intracellular antiviral responses. Among the challenges to the host cell is the viral DNA genome, which is viewed as DNA damage and elicits a cellular response to inhibit replication. Adenovirus therefore encodes proteins that dismantle the cellular DNA damage machinery. Studying virus-host interactions has yielded insights into the molecular functioning of fundamental cellular mechanisms. In addition, it has suggested ways that viral cytotoxicity can be exploited to offer a selective means of restricted growth in tumor cells as a therapy against cancer. In this review, we discuss aspects of the intracellular response that are unique to adenovirus infection and how adenoviral proteins produced from the early region E4 act to neutralize antiviral defenses, with a particular focus on DNA damage signaling.

摘要

DNA病毒促进细胞周期进程,刺激非计划的DNA合成,并向细胞呈现大量外源性DNA。这些损伤引发由控制细胞稳态的细胞因子介导的强烈反应。为确保有效感染,腺病毒已开发出灭活这些细胞内抗病毒反应的方法。宿主细胞面临的挑战之一是病毒DNA基因组,它被视为DNA损伤并引发抑制复制的细胞反应。因此,腺病毒编码可拆解细胞DNA损伤机制的蛋白质。研究病毒与宿主的相互作用已使人们深入了解基本细胞机制的分子功能。此外,它还提出了利用病毒细胞毒性作为针对癌症的疗法,在肿瘤细胞中提供一种限制生长的选择性手段的方法。在本综述中,我们讨论腺病毒感染所特有的细胞内反应的各个方面,以及早期区域E4产生的腺病毒蛋白如何中和抗病毒防御,特别关注DNA损伤信号传导。

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