自噬
泛素
DNA损伤
生物
免疫系统
细胞生物学
溶酶体
信号
免疫学
DNA
基因
遗传学
生物化学
酶
细胞凋亡
作者
Shunbin Ning,Ling Wang
出处
期刊:Current Cancer Drug Targets
[Bentham Science]
日期:2018-10-18
卷期号:19 (6): 468-478
被引量:28
标识
DOI:10.2174/1568009618666181016164920
摘要
The multifunctional signaling hub p62 is well recognized as a ubiquitin sensor and a selective autophagy receptor. As a ubiquitin sensor, p62 promotes NFκB activation by facilitating TRAF6 ubiquitination and aggregation. As a selective autophagy receptor, p62 sorts ubiquitinated substrates including p62 itself for lysosome-mediated degradation. p62 plays crucial roles in myriad cellular processes including DNA damage response, aging/senescence, infection and immunity, chronic inflammation, and cancerogenesis, dependent on or independent of autophagy. Targeting p62-mediated autophagy may represent a promising strategy for clinical interventions of different cancers. In this review, we summarize the transcriptional and post-translational regulation of p62, and its mechanistic roles in cancers, with the emphasis on its roles in regulation of DNA damage response and its connection to the cGAS-STING-mediated antitumor immune response, which is promising for cancer vaccine design.
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