Roles of the cGAS-STING Pathway in Cancer Immunosurveillance and Immunotherapy

Author:

Yum Seoyun1,Li Minghao1,Frankel Arthur E.2,Chen Zhijian J.13

Affiliation:

1. Department of Molecular Biology and Center for Inflammation Research, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA;

2. Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, USA;

3. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA

Abstract

Cyclic GMP-AMP synthase (cGAS) is a cytosolic DNA sensor that initiates innate immune responses. DNA-bound cGAS produces cyclic GMP-AMP (cGAMP), which activates stimulator of interferon genes (STING) to induce inflammatory cytokines and other immune mediators. cGAS detects DNA without sequence specificity and responds to both cytosolic foreign DNA from pathogens and self-DNA leaked into the cytosol due to genome instability or cellular damage. Because of the diverse sources of cytosolic DNA, the cGAS-STING pathway plays a critical role during infection, autoimmune diseases, and senescence. Moreover, cGAS detects tumor-derived DNA and stimulates endogenous antitumor immunity. Thus, the cGAS-STING pathway is a promising target for cancer immunotherapy. Here, we review the role of the cGAS-STING pathway in various diseases and highlight various approaches targeting the cGAS-STING pathway for cancer therapy.

Publisher

Annual Reviews

Subject

Cancer Research,Cell Biology,Oncology

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