共 141 条
For Better orWorse: Modulation of the Host DNA Damage Response by Human Papillomavirus
被引:11
作者:

Studstill, Caleb J.
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机构:
Univ North Carolina, Dept Microbiol & Immunol, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA Univ North Carolina, Dept Microbiol & Immunol, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA

Moody, Cary A.
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机构:
Univ North Carolina, Dept Microbiol & Immunol, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA Univ North Carolina, Dept Microbiol & Immunol, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
机构:
[1] Univ North Carolina, Dept Microbiol & Immunol, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27515 USA
关键词:
human papillomavirus;
DNA damage response;
innate immune activation;
HPV-associated cancers;
viral life cycle;
COMMON FRAGILE SITES;
HOMOLOGOUS RECOMBINATION;
REPLICATION-STRESS;
E7;
ONCOPROTEIN;
PRODUCTIVE REPLICATION;
GENOMIC INSTABILITY;
REPAIR FACTORS;
BREAK REPAIR;
R-LOOPS;
CANCER;
D O I:
10.1146/annurev-virology-111821-103452
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
High-risk human papillomaviruses (HPVs) are associated with several human cancers. HPVs are small, DNA viruses that rely on host cell machinery for viral replication. The HPV life cycle takes place in the stratified epithelium, which is composed of different cell states, including terminally differentiating cells that are no longer active in the cell cycle. HPVs have evolved mechanisms to persist and replicate in the stratified epithelium by hijacking and modulating cellular pathways, including the DNA damage response (DDR). HPVs activate and exploit DDR pathways to promote viral replication, which in turn increases the susceptibility of the host cell to genomic instability and carcinogenesis. Here, we review recent advances in our understanding of the regulation of the host cell DDR by high-risk HPVs during the viral life cycle and discuss the potential cellular consequences of modulating DDR pathways.
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页码:325 / 345
页数:21
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