Skip to content
2000
Volume 19, Issue 6
  • ISSN: 1568-0096
  • E-ISSN: 1873-5576

Abstract

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.

Loading

Article metrics loading...

/content/journals/ccdt/10.2174/1568009618666181016164920
2019-07-01
2025-12-08
Loading full text...

Full text loading...

/content/journals/ccdt/10.2174/1568009618666181016164920
Loading

  • Article Type:
    Review Article
Keyword(s): antitumor immune response; autophagy; cancer vaccine design; p62; ROS; ubiquitination
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test