The interplay between autophagy and cGAS-STING signaling and its implications for cancer

Front Immunol. 2024 Apr 10:15:1356369. doi: 10.3389/fimmu.2024.1356369. eCollection 2024.

Abstract

Autophagy is an intracellular process that targets various cargos for degradation, including members of the cGAS-STING signaling cascade. cGAS-STING senses cytosolic double-stranded DNA and triggers an innate immune response through type I interferons. Emerging evidence suggests that autophagy plays a crucial role in regulating and fine-tuning cGAS-STING signaling. Reciprocally, cGAS-STING pathway members can actively induce canonical as well as various non-canonical forms of autophagy, establishing a regulatory network of feedback mechanisms that alter both the cGAS-STING and the autophagic pathway. The crosstalk between autophagy and the cGAS-STING pathway impacts a wide variety of cellular processes such as protection against pathogenic infections as well as signaling in neurodegenerative disease, autoinflammatory disease and cancer. Here we provide a comprehensive overview of the mechanisms involved in autophagy and cGAS-STING signaling, with a specific focus on the interactions between the two pathways and their importance for cancer.

Keywords: autophagy; cGAS/STING signaling; cancer; innate immunity; radiotherapy.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy* / immunology
  • Humans
  • Immunity, Innate
  • Membrane Proteins* / metabolism
  • Neoplasms* / immunology
  • Neoplasms* / metabolism
  • Neoplasms* / pathology
  • Nucleotidyltransferases* / metabolism
  • Signal Transduction*

Substances

  • Nucleotidyltransferases
  • Membrane Proteins
  • cGAS protein, human
  • STING1 protein, human

Grants and funding

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