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Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer
Enteric glia are a distinct population of peripheral glial cells in the enteric nervous system that regulate intestinal homeostasis, epithelial barrier integrity, and gut defense. Given these unique attributes, we investigated the impact of enteric glia depletion on tumor development in azoxymethane...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691584/ https://www.ncbi.nlm.nih.gov/pubmed/33282743 http://dx.doi.org/10.3389/fonc.2020.595892 |
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author | Yuan, Robert Bhattacharya, Nupur Kenkel, Justin A. Shen, Jeanne DiMaio, Michael A. Bagchi, Sreya Prestwood, Tyler R. Habtezion, Aida Engleman, Edgar G. |
author_facet | Yuan, Robert Bhattacharya, Nupur Kenkel, Justin A. Shen, Jeanne DiMaio, Michael A. Bagchi, Sreya Prestwood, Tyler R. Habtezion, Aida Engleman, Edgar G. |
author_sort | Yuan, Robert |
collection | PubMed |
description | Enteric glia are a distinct population of peripheral glial cells in the enteric nervous system that regulate intestinal homeostasis, epithelial barrier integrity, and gut defense. Given these unique attributes, we investigated the impact of enteric glia depletion on tumor development in azoxymethane/dextran sodium sulfate (AOM/DSS)-treated mice, a classical model of colorectal cancer (CRC). Depleting GFAP(+) enteric glia resulted in a profoundly reduced tumor burden in AOM/DSS mice and additionally reduced adenomas in the Apc(Min)(/+) mouse model of familial adenomatous polyposis, suggesting a tumor-promoting role for these cells at an early premalignant stage. This was confirmed in further studies of AOM/DSS mice, as enteric glia depletion did not affect the properties of established malignant tumors but did result in a marked reduction in the development of precancerous dysplastic lesions. Surprisingly, the protective effect of enteric glia depletion was not dependent on modulation of anti-tumor immunity or intestinal inflammation. These findings reveal that GFAP(+) enteric glia play a critical pro-tumorigenic role during early CRC development and identify these cells as a potential target for CRC prevention. |
format | Online Article Text |
id | pubmed-7691584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76915842020-12-04 Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer Yuan, Robert Bhattacharya, Nupur Kenkel, Justin A. Shen, Jeanne DiMaio, Michael A. Bagchi, Sreya Prestwood, Tyler R. Habtezion, Aida Engleman, Edgar G. Front Oncol Oncology Enteric glia are a distinct population of peripheral glial cells in the enteric nervous system that regulate intestinal homeostasis, epithelial barrier integrity, and gut defense. Given these unique attributes, we investigated the impact of enteric glia depletion on tumor development in azoxymethane/dextran sodium sulfate (AOM/DSS)-treated mice, a classical model of colorectal cancer (CRC). Depleting GFAP(+) enteric glia resulted in a profoundly reduced tumor burden in AOM/DSS mice and additionally reduced adenomas in the Apc(Min)(/+) mouse model of familial adenomatous polyposis, suggesting a tumor-promoting role for these cells at an early premalignant stage. This was confirmed in further studies of AOM/DSS mice, as enteric glia depletion did not affect the properties of established malignant tumors but did result in a marked reduction in the development of precancerous dysplastic lesions. Surprisingly, the protective effect of enteric glia depletion was not dependent on modulation of anti-tumor immunity or intestinal inflammation. These findings reveal that GFAP(+) enteric glia play a critical pro-tumorigenic role during early CRC development and identify these cells as a potential target for CRC prevention. Frontiers Media S.A. 2020-11-13 /pmc/articles/PMC7691584/ /pubmed/33282743 http://dx.doi.org/10.3389/fonc.2020.595892 Text en Copyright © 2020 Yuan, Bhattacharya, Kenkel, Shen, DiMaio, Bagchi, Prestwood, Habtezion and Engleman http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yuan, Robert Bhattacharya, Nupur Kenkel, Justin A. Shen, Jeanne DiMaio, Michael A. Bagchi, Sreya Prestwood, Tyler R. Habtezion, Aida Engleman, Edgar G. Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title | Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title_full | Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title_fullStr | Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title_full_unstemmed | Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title_short | Enteric Glia Play a Critical Role in Promoting the Development of Colorectal Cancer |
title_sort | enteric glia play a critical role in promoting the development of colorectal cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691584/ https://www.ncbi.nlm.nih.gov/pubmed/33282743 http://dx.doi.org/10.3389/fonc.2020.595892 |
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