PTMs of PD-1/PD-L1 and PROTACs application for improving cancer immunotherapy

Front Immunol. 2024 Apr 4:15:1392546. doi: 10.3389/fimmu.2024.1392546. eCollection 2024.

Abstract

Immunotherapy has been developed, which harnesses and enhances the innate powers of the immune system to fight disease, particularly cancer. PD-1 (programmed death-1) and PD-L1 (programmed death ligand-1) are key components in the regulation of the immune system, particularly in the context of cancer immunotherapy. PD-1 and PD-L1 are regulated by PTMs, including phosphorylation, ubiquitination, deubiquitination, acetylation, palmitoylation and glycosylation. PROTACs (Proteolysis Targeting Chimeras) are a type of new drug design technology. They are specifically engineered molecules that target specific proteins within a cell for degradation. PROTACs have been designed and demonstrated their inhibitory activity against the PD-1/PD-L1 pathway, and showed their ability to degrade PD-1/PD-L1 proteins. In this review, we describe how PROTACs target PD-1 and PD-L1 proteins to improve the efficacy of immunotherapy. PROTACs could be a novel strategy to combine with radiotherapy, chemotherapy and immunotherapy for cancer patients.

Keywords: PD-1; PD-L1; PROTAC; immunotherapy; ubiquitination.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen* / metabolism
  • Humans
  • Immunotherapy
  • Neoplasms* / drug therapy
  • Programmed Cell Death 1 Receptor / metabolism
  • Proteolysis Targeting Chimera

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor
  • Proteolysis Targeting Chimera

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.