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Mitochondrial control of innate immune signaling by irradiated cancer cells
Type I interferon (IFN) release by irradiated cancer cells is paramount for radiation therapy to elicit anticancer immunity. Our findings demonstrate that mitochondrial outer membrane permeabilization (MOMP) triggered by RT enables exposure of mitochondrial DNA to the cytosol, hence setting off CGAS...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458622/ https://www.ncbi.nlm.nih.gov/pubmed/32923160 http://dx.doi.org/10.1080/2162402X.2020.1797292 |
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author | Yamazaki, Takahiro Galluzzi, Lorenzo |
author_facet | Yamazaki, Takahiro Galluzzi, Lorenzo |
author_sort | Yamazaki, Takahiro |
collection | PubMed |
description | Type I interferon (IFN) release by irradiated cancer cells is paramount for radiation therapy to elicit anticancer immunity. Our findings demonstrate that mitochondrial outer membrane permeabilization (MOMP) triggered by RT enables exposure of mitochondrial DNA to the cytosol, hence setting off CGAS-driven type I IFN synthesis. These data point to the existence of a therapeutically actionable mitochondrial checkpoint that restricts innate immune signaling in irradiated cancer cells. |
format | Online Article Text |
id | pubmed-7458622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74586222020-09-11 Mitochondrial control of innate immune signaling by irradiated cancer cells Yamazaki, Takahiro Galluzzi, Lorenzo Oncoimmunology Editorial Type I interferon (IFN) release by irradiated cancer cells is paramount for radiation therapy to elicit anticancer immunity. Our findings demonstrate that mitochondrial outer membrane permeabilization (MOMP) triggered by RT enables exposure of mitochondrial DNA to the cytosol, hence setting off CGAS-driven type I IFN synthesis. These data point to the existence of a therapeutically actionable mitochondrial checkpoint that restricts innate immune signaling in irradiated cancer cells. Taylor & Francis 2020-07-22 /pmc/articles/PMC7458622/ /pubmed/32923160 http://dx.doi.org/10.1080/2162402X.2020.1797292 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Editorial Yamazaki, Takahiro Galluzzi, Lorenzo Mitochondrial control of innate immune signaling by irradiated cancer cells |
title | Mitochondrial control of innate immune signaling by irradiated cancer cells |
title_full | Mitochondrial control of innate immune signaling by irradiated cancer cells |
title_fullStr | Mitochondrial control of innate immune signaling by irradiated cancer cells |
title_full_unstemmed | Mitochondrial control of innate immune signaling by irradiated cancer cells |
title_short | Mitochondrial control of innate immune signaling by irradiated cancer cells |
title_sort | mitochondrial control of innate immune signaling by irradiated cancer cells |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458622/ https://www.ncbi.nlm.nih.gov/pubmed/32923160 http://dx.doi.org/10.1080/2162402X.2020.1797292 |
work_keys_str_mv | AT yamazakitakahiro mitochondrialcontrolofinnateimmunesignalingbyirradiatedcancercells AT galluzzilorenzo mitochondrialcontrolofinnateimmunesignalingbyirradiatedcancercells |