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Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis
Dietary iron intake is closely related to the incidence of colorectal cancer. However, the interactions among dietary iron, gut microbiota, and epithelial cells in promoting tumorigenesis have rarely been discussed. Here, we report that gut microbiota plays a crucial role in promoting colorectal tum...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269393/ https://www.ncbi.nlm.nih.gov/pubmed/37312410 http://dx.doi.org/10.1080/19490976.2023.2221978 |
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author | Liu, Chen Gong, Junli Zhang, Qiang Chen, Guangyuan Yin, Shengmei Luo, Zhanhao Zeng, Wanyi Yu, Jing Lan, Ping He, Zhen |
author_facet | Liu, Chen Gong, Junli Zhang, Qiang Chen, Guangyuan Yin, Shengmei Luo, Zhanhao Zeng, Wanyi Yu, Jing Lan, Ping He, Zhen |
author_sort | Liu, Chen |
collection | PubMed |
description | Dietary iron intake is closely related to the incidence of colorectal cancer. However, the interactions among dietary iron, gut microbiota, and epithelial cells in promoting tumorigenesis have rarely been discussed. Here, we report that gut microbiota plays a crucial role in promoting colorectal tumorigenesis in multiple mice models under excessive dietary iron intake. Gut microbiota modulated by excessive dietary iron are pathogenic, irritating the permeability of the gut barrier and causing leakage of lumen bacteria. Mechanistically, epithelial cells released more secretory leukocyte protease inhibitor (SLPI) to combat the leaked bacteria and limit inflammation. The upregulated SLPI acted as a pro-tumorigenic factor and promoted colorectal tumorigenesis by activating the MAPK signaling pathway. Moreover, excessive dietary iron significantly depleted Akkermansiaceae in the gut microbiota; while supplementation with Akkermansia muciniphila could successfully attenuate the tumorigenic effect from excessive dietary iron. Overall, excessive dietary iron perturbs diet – microbiome–epithelium interactions, which contributes to intestinal tumor initiation. |
format | Online Article Text |
id | pubmed-10269393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-102693932023-06-16 Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis Liu, Chen Gong, Junli Zhang, Qiang Chen, Guangyuan Yin, Shengmei Luo, Zhanhao Zeng, Wanyi Yu, Jing Lan, Ping He, Zhen Gut Microbes Research Paper Dietary iron intake is closely related to the incidence of colorectal cancer. However, the interactions among dietary iron, gut microbiota, and epithelial cells in promoting tumorigenesis have rarely been discussed. Here, we report that gut microbiota plays a crucial role in promoting colorectal tumorigenesis in multiple mice models under excessive dietary iron intake. Gut microbiota modulated by excessive dietary iron are pathogenic, irritating the permeability of the gut barrier and causing leakage of lumen bacteria. Mechanistically, epithelial cells released more secretory leukocyte protease inhibitor (SLPI) to combat the leaked bacteria and limit inflammation. The upregulated SLPI acted as a pro-tumorigenic factor and promoted colorectal tumorigenesis by activating the MAPK signaling pathway. Moreover, excessive dietary iron significantly depleted Akkermansiaceae in the gut microbiota; while supplementation with Akkermansia muciniphila could successfully attenuate the tumorigenic effect from excessive dietary iron. Overall, excessive dietary iron perturbs diet – microbiome–epithelium interactions, which contributes to intestinal tumor initiation. Taylor & Francis 2023-06-13 /pmc/articles/PMC10269393/ /pubmed/37312410 http://dx.doi.org/10.1080/19490976.2023.2221978 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Paper Liu, Chen Gong, Junli Zhang, Qiang Chen, Guangyuan Yin, Shengmei Luo, Zhanhao Zeng, Wanyi Yu, Jing Lan, Ping He, Zhen Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title | Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title_full | Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title_fullStr | Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title_full_unstemmed | Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title_short | Dietary iron modulates gut microbiota and induces SLPI secretion to promote colorectal tumorigenesis |
title_sort | dietary iron modulates gut microbiota and induces slpi secretion to promote colorectal tumorigenesis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269393/ https://www.ncbi.nlm.nih.gov/pubmed/37312410 http://dx.doi.org/10.1080/19490976.2023.2221978 |
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