人类乳突病毒利用DNA损伤修复机制完成其生命周期
Saved in:
Published in | 浙江大学学报:B卷英文版 Vol. 18; no. 3; pp. 215 - 232 |
---|---|
Main Author | |
Format | Journal Article |
Language | English |
Published |
2017
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Bibliography: | The DNA damage response (DDR) is activated when DNA is altered by intrinsic or extrinsic agents. This pathway is a complex signaling network and plays important roles in genome stability, tumor transformation, and cell cycle regulation. Human papillomaviruses (HPVs) are the main etiological agents of cervical cancer. Cervical cancer ranks as the fourth most common cancer among women and the second most frequent cause of cancer-related death worldwide. Over 200 types of HPVs have been identified and about one third of these infect the genital tract. The HPV life cycle is associated with epithelial differentiation. Recent studies have shown that HPVs deregulate the DDR to achieve a productive life cycle. In this review, I summarize current findings about how HPVs mediate the ataxia- telangiectasia mutated kinase (ATM) and the ATM- and RAD3-related kinase (ATR) DDRs, and focus on the roles that ATM and ATR signalings play in HPV viral replication. In addition, I demonstrate that the signal transducer and acti- vator of transcription-5 (STAT)-5, an important immune regulator, can promote ATM and ATR activations through different mechanisms. These findings may provide novel opportunities for development of new therapeutic targets for HPV-related cancers. 33-1356/Q Papillomavirus; DNA damage; Amplification; Differentiation; ATM/CHK2; ATR/CHK1; STAT-5 |
---|---|
ISSN: | 1673-1581 1862-1783 |