Taking the STING out of radiotherapy: STING checkpoints mediate radiation resistance

The cyclic GMP-AMP synthase/stimulator of interferon genes (cGAS/STING) pathway is a critical driver of type I interferon (IFN-I) and antitumor CD8+ T cell responses after radiotherapy (RT). In this issue of the JCI, two reports describe mechanisms that restrained STING signaling and abrogated antitumor immunity after RT. Wen, Wang, and colleagues discovered that IFN-I mediated the induction of YTHDF1, an RNA N6-methyladenosine-binding protein, in DCs after RT promoted cathepsin-mediated STING degradation. Zhang, Deng, Wu, and colleagues discovered that hemeoxygenase 1 (HO-1) was induced and proteolytically cleaved after RT to suppress cGAS cytoplasmic export as well as STING oligomerization at the ER. Blocking the STING-suppressive functions of YTHDF1 and HO-1, respectively, improved antitumor T cell immunity and tumor control after RT. Together, these studies support the development of clinical avenues to sustain STING signaling during RT, a standard treatment for approximately 50% of malignancies.

Authors

Publication Details

Journal
Journal of Clinical Investigation
Published
2024-12-01
DOI
https://doi.org/10.1172/jci186547
Citations
5
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
1.20

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article

Taking the STING out of radiotherapy: STING checkpoints mediate radiation resistance

Michael C. Brown, Justin Low, David M. Ashley, Michelle Bowie
5 citations
Journal of Clinical Investigation
interferon and immune responses
1.20
article

Taking the STING out of radiotherapy: STING checkpoints mediate radiation resistance

Michael C. Brown, Justin Low, David M. Ashley, Michelle Bowie
article en
5 citations

Abstract

The cyclic GMP-AMP synthase/stimulator of interferon genes (cGAS/STING) pathway is a critical driver of type I interferon (IFN-I) and antitumor CD8+ T cell responses after radiotherapy (RT). In this issue of the JCI, two reports describe mechanisms that restrained STING signaling and abrogated antitumor immunity after RT. Wen, Wang, and colleagues discovered that IFN-I mediated the induction of YTHDF1, an RNA N6-methyladenosine-binding protein, in DCs after RT promoted cathepsin-mediated STING degradation. Zhang, Deng, Wu, and colleagues discovered that hemeoxygenase 1 (HO-1) was induced and proteolytically cleaved after RT to suppress cGAS cytoplasmic export as well as STING oligomerization at the ER. Blocking the STING-suppressive functions of YTHDF1 and HO-1, respectively, improved antitumor T cell immunity and tumor control after RT. Together, these studies support the development of clinical avenues to sustain STING signaling during RT, a standard treatment for approximately 50% of malignancies.

Journal of Clinical InvestigationVol. 134(23)
Alex's Lemonade Stand Foundation for Childhood Cancer, Strong, National Institutes of Health, School of Medicine, Duke University, National Cancer Institute
Openalex Percentile: Top 20%
interferon and immune responses
1.20
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Taking the STING out of radiotherapy: STING checkpoints mediate radiation resistance — Michael C. Brown, Justin Low, et al. · Journal of Clinical Investigation (2024) | TGRS Research Map | TGRS