Interferon regulatory factor 1 regulates PANoptosis to prevent colorectal cancer
Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emergin...
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| Vydáno v: | JCI insight Ročník 5; číslo 12 |
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| Hlavní autoři: | , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
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United States
American Society for Clinical Investigation
18.06.2020
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| ISSN: | 2379-3708, 2379-3708 |
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| Abstract | Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1-/- mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis. |
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| AbstractList | Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1-/- mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis.Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1-/- mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis. Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1–/– mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis. IRF1-deficient mice are hypersusceptible to colorectal tumorigenesis, with attenuated cell death in the colons caused by defective PANoptosis. Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic mutations and altered IRF1 function are associated with several cancers. Although the function of IRF1 in the immunobiology of cancer is emerging, IRF1-specific mechanisms regulating tumorigenesis and tissue homeostasis in vivo are not clear. Here, we found that mice lacking IRF1 were hypersusceptible to colorectal tumorigenesis. IRF1 functions in both the myeloid and epithelial compartments to confer protection against AOM/DSS-induced colorectal tumorigenesis. We further found that IRF1 also prevents tumorigenesis in a spontaneous mouse model of colorectal cancer. The attenuated cell death in the colons of Irf1–/– mice was due to defective pyroptosis, apoptosis, and necroptosis (PANoptosis). IRF1 does not regulate inflammation and the inflammasome in the colon. Overall, our study identified IRF1 as an upstream regulator of PANoptosis to induce cell death during colitis-associated tumorigenesis. |
| Author | Banoth, Balaji Malireddi, R.K. Subbarao Kanneganti, Thirumala-Devi Burton, Amanda R. Vogel, Peter Samir, Parimal Lee, Ein Karki, Rajendra Tuladhar, Shraddha Sharma, Bhesh Raj Mummareddy, Harisankeerth |
| AuthorAffiliation | 4 Animal Resources Center and Veterinary Pathology Core, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA 2 Integrated Biomedical Sciences Program, University of Tennessee Health Science Center, Memphis, Tennessee, USA 1 Department of Immunology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA 3 Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA |
| AuthorAffiliation_xml | – name: 2 Integrated Biomedical Sciences Program, University of Tennessee Health Science Center, Memphis, Tennessee, USA – name: 4 Animal Resources Center and Veterinary Pathology Core, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA – name: 1 Department of Immunology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA – name: 3 Emory College of Arts and Sciences, Emory University, Atlanta, Georgia, USA |
| Author_xml | – sequence: 1 givenname: Rajendra surname: Karki fullname: Karki, Rajendra – sequence: 2 givenname: Bhesh Raj surname: Sharma fullname: Sharma, Bhesh Raj – sequence: 3 givenname: Ein surname: Lee fullname: Lee, Ein – sequence: 4 givenname: Balaji surname: Banoth fullname: Banoth, Balaji – sequence: 5 givenname: R.K. Subbarao surname: Malireddi fullname: Malireddi, R.K. Subbarao – sequence: 6 givenname: Parimal surname: Samir fullname: Samir, Parimal – sequence: 7 givenname: Shraddha surname: Tuladhar fullname: Tuladhar, Shraddha – sequence: 8 givenname: Harisankeerth surname: Mummareddy fullname: Mummareddy, Harisankeerth – sequence: 9 givenname: Amanda R. surname: Burton fullname: Burton, Amanda R. – sequence: 10 givenname: Peter orcidid: 0000-0002-7535-0545 surname: Vogel fullname: Vogel, Peter – sequence: 11 givenname: Thirumala-Devi surname: Kanneganti fullname: Kanneganti, Thirumala-Devi |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32554929$$D View this record in MEDLINE/PubMed |
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| Keywords | Innate immunity Oncology Immunology Colorectal cancer Cancer |
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| Snippet | Interferon regulatory factor 1 (IRF1) regulates diverse biological functions, including modulation of cellular responses involved in tumorigenesis. Genetic... |
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| SubjectTerms | Apoptosis Cancer Cell death Colitis Colorectal cancer Colorectal carcinoma Homeostasis Infections Inflammasomes Inflammation Inflammatory bowel disease Inflammatory diseases Interferon Interferon regulatory factor Interferon regulatory factor 1 Kinases Medical prognosis Mutation Necroptosis Proteins Pyroptosis Transcription factors Tumorigenesis Tumors |
| Title | Interferon regulatory factor 1 regulates PANoptosis to prevent colorectal cancer |
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