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Title: | Type 2 Innate Lymphoid Cells Protect against Colorectal Cancer Progression and Predict Improved Patient Survival. | Austin Authors: | Huang, Qiutong;Jacquelot, Nicolas;Preaudet, Adele;Hediyeh-Zadeh, Soroor;Souza-Fonseca-Guimaraes, Fernando;McKenzie, Andrew N J;Hansbro, Philip M;Davis, Melissa J;Mielke, Lisa A;Putoczki, Tracy L;Belz, Gabrielle T | Affiliation: | Walter and Eliza Hall Institute of Medical Research, Parkville, Melbourne 3052, Australia Department of Medical Biology, University of Melbourne, Parkville, Melbourne 3010, Australia The University of Queensland Diamantina Institute, 37 Kent Street, Woolloongabba, Brisbane 4102, Australia Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK Center for Inflammation, Centenary Institute and the School of Life Sciences, University of Technology Sydney, Sydney 2050, Australia Department of Clinical Pathology, University of Melbourne, Parkville, Melbourne 3010, Australia Olivia Newton-John Cancer Research Institute La Trobe University School of Cancer Medicine, Heidelberg 3084, Australia |
Issue Date: | 1-Feb-2021 | Date: | 2021-02-01 | Publication information: | Cancers 2021; 13(3): 559 | Abstract: | Chronic inflammation of the gastrointestinal (GI) tract contributes to colorectal cancer (CRC) progression. While the role of adaptive T cells in CRC is now well established, the role of innate immune cells, specifically innate lymphoid cells (ILCs), is not well understood. To define the role of ILCs in CRC we employed complementary heterotopic and chemically-induced CRC mouse models. We discovered that ILCs were abundant in CRC tumours and contributed to anti-tumour immunity. We focused on ILC2 and showed that ILC2-deficient mice developed a higher tumour burden compared with littermate wild-type controls. We generated an ILC2 gene signature and using machine learning models revealed that CRC patients with a high intratumor ILC2 gene signature had a favourable clinical prognosis. Collectively, our results highlight a critical role for ILC2 in CRC, suggesting a potential new avenue to improve clinical outcomes through ILC2-agonist based therapeutic approaches. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/25793 | DOI: | 10.3390/cancers13030559 | ORCID: | 0000-0003-0282-1892 0000-0002-2037-8946 0000-0002-9522-9320 0000-0003-1639-4932 |
Journal: | Cancers | PubMed URL: | 33535624 | ISSN: | 2072-6694 | Type: | Journal Article | Subjects: | IL-13 IL-5 ILC2 colitis-associated cancer colon cancer inflammation |
Appears in Collections: | Journal articles |
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