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Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status
BACKGROUND: Carrying excess body weight is a strong risk factor for colorectal cancer (CRC) development with ~11% of CRC cases in Europe linked to being overweight. The mechanisms through which excess body weight influences CRC development are not well understood but studies suggest the involvement...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861504/ https://www.ncbi.nlm.nih.gov/pubmed/35211486 http://dx.doi.org/10.3389/fmed.2021.800566 |
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author | Shaw, Sophie Berry, Susan Thomson, John Murray, Graeme I. El-Omar, Emad Hold, Georgina L. |
author_facet | Shaw, Sophie Berry, Susan Thomson, John Murray, Graeme I. El-Omar, Emad Hold, Georgina L. |
author_sort | Shaw, Sophie |
collection | PubMed |
description | BACKGROUND: Carrying excess body weight is a strong risk factor for colorectal cancer (CRC) development with ~11% of CRC cases in Europe linked to being overweight. The mechanisms through which excess body weight influences CRC development are not well understood but studies suggest the involvement of the presence of chronic low-grade inflammation and changes in the gut microbiota are involved. AIM: To compare the mucosal associated microbiota of patients with CRC to understand whether carrying excess body weight was associated with a unique CRC microbial signature. METHODS: Microbiota signatures from colonic mucosal biopsies of CRC lesions and adjacent normal mucosal samples from 20 patients with overt CRC were compared with 11 healthy controls to see if having a BMI of >25 kg/m(2) influenced colonic microbial composition. RESULTS: Colonic mucosa samples from patients with CRC confirmed previously reported over-abundance of Fusobacteria associated with CRC but also an increase in Fusobacteria and Prevotella were associated with a BMI of >25 kg/m(2). Correlation analysis of bacterial taxa indicated co-exclusive relationships were more common in CRC patients with a BMI >25 kg/m(2) with an increase in transphylum relationships also seen in this patient group. CONCLUSIONS: The findings suggest that gut microbiota composition in patients with CRC is influenced by BMI status. Further understanding/defining these differences will provide valuable information in terms of developing novel pre-onset screening and providing post-manifestation therapeutic intervention. |
format | Online Article Text |
id | pubmed-8861504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88615042022-02-23 Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status Shaw, Sophie Berry, Susan Thomson, John Murray, Graeme I. El-Omar, Emad Hold, Georgina L. Front Med (Lausanne) Medicine BACKGROUND: Carrying excess body weight is a strong risk factor for colorectal cancer (CRC) development with ~11% of CRC cases in Europe linked to being overweight. The mechanisms through which excess body weight influences CRC development are not well understood but studies suggest the involvement of the presence of chronic low-grade inflammation and changes in the gut microbiota are involved. AIM: To compare the mucosal associated microbiota of patients with CRC to understand whether carrying excess body weight was associated with a unique CRC microbial signature. METHODS: Microbiota signatures from colonic mucosal biopsies of CRC lesions and adjacent normal mucosal samples from 20 patients with overt CRC were compared with 11 healthy controls to see if having a BMI of >25 kg/m(2) influenced colonic microbial composition. RESULTS: Colonic mucosa samples from patients with CRC confirmed previously reported over-abundance of Fusobacteria associated with CRC but also an increase in Fusobacteria and Prevotella were associated with a BMI of >25 kg/m(2). Correlation analysis of bacterial taxa indicated co-exclusive relationships were more common in CRC patients with a BMI >25 kg/m(2) with an increase in transphylum relationships also seen in this patient group. CONCLUSIONS: The findings suggest that gut microbiota composition in patients with CRC is influenced by BMI status. Further understanding/defining these differences will provide valuable information in terms of developing novel pre-onset screening and providing post-manifestation therapeutic intervention. Frontiers Media S.A. 2022-02-08 /pmc/articles/PMC8861504/ /pubmed/35211486 http://dx.doi.org/10.3389/fmed.2021.800566 Text en Copyright © 2022 Shaw, Berry, Thomson, Murray, El-Omar and Hold. https://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 | Medicine Shaw, Sophie Berry, Susan Thomson, John Murray, Graeme I. El-Omar, Emad Hold, Georgina L. Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title | Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title_full | Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title_fullStr | Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title_full_unstemmed | Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title_short | Gut Mucosal Microbiome Signatures of Colorectal Cancer Differ According to BMI Status |
title_sort | gut mucosal microbiome signatures of colorectal cancer differ according to bmi status |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861504/ https://www.ncbi.nlm.nih.gov/pubmed/35211486 http://dx.doi.org/10.3389/fmed.2021.800566 |
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