Human polyomavirus modulation of the host DNA damage response

被引:0
|
作者
Danyal Tahseen
Peter L. Rady
Stephen K. Tyring
机构
[1] University of Texas Medical School At Houston,Department of Dermatology
来源
Virus Genes | 2020年 / 56卷
关键词
Human polyomavirus; DNA damage response; MCPyV; BKPyV; JCPyV; TSPyV; HCPyV; Human cancer; Virus–host cell interactions; Oncogenes; Large T antigen; Small T antigen;
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学科分类号
摘要
The human DNA damage response (DDR) is a complex signaling network constituting many factors responsible for the preservation of genomic integrity. Human polyomaviruses (HPyVs) are able to harness the DDR machinery during their infectious cycle by expressing an array of tumor (T) antigens. These molecular interactions between human polyomavirus T antigens and the DDR create conditions that promote viral replication at the expense of host genomic stability to cause disease as well as carcinogenesis in the cases of the Merkel cell polyomavirus and BK polyomavirus. This review focuses on the six HPyVs with disease association, emphasizing strain-dependent differences in their selective manipulation of the DDR. Appreciation of the HPyV–DDR interface at a molecular scale is conducive to the development of novel therapeutic approaches.
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页码:128 / 135
页数:7
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