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Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences
Various studies have shown the interplay between the intestinal microbiome, environmental factors, and genetic changes in colorectal cancer (CRC) development. In this review, we highlight the various gut and oral microbiota associated with CRC and colorectal adenomas, and their proposed molecular me...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918999/ https://www.ncbi.nlm.nih.gov/pubmed/35317317 http://dx.doi.org/10.4251/wjgo.v14.i2.375 |
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author | Tortora, Sofia C Bodiwala, Vimal M Quinn, Andrew Martello, Laura A Vignesh, Shivakumar |
author_facet | Tortora, Sofia C Bodiwala, Vimal M Quinn, Andrew Martello, Laura A Vignesh, Shivakumar |
author_sort | Tortora, Sofia C |
collection | PubMed |
description | Various studies have shown the interplay between the intestinal microbiome, environmental factors, and genetic changes in colorectal cancer (CRC) development. In this review, we highlight the various gut and oral microbiota associated with CRC and colorectal adenomas, and their proposed molecular mechanisms in relation to the processes of “the hallmarks of cancer”, and differences in microbial diversity and abundance between race/ethnicity. Patients with CRC showed increased levels of Bacteroides, Prevotella, Escherichia coli, enterotoxigenic Bacteroides fragilis, Streptococcus gallolyticus, Enterococcus faecalis, Fusobacterium nucleatum (F. nucleatum) and Clostridium difficile. Higher levels of Bacteroides have been found in African American (AA) compared to Caucasian American (CA) patients. Pro-inflammatory bacteria such as F. nucleatum and Enterobacter species were significantly higher in AAs. Also, AA patients have been shown to have decreased microbial diversity compared to CA patients. Some studies have shown that using microbiome profiles in conjunction with certain risk factors such as age, race and body mass index may help predict healthy colon vs one with adenomas or carcinomas. Periodontitis is one of the most common bacterial infections in humans and is more prevalent in Non-Hispanic-Blacks as compared to Non-Hispanic Whites. This condition causes increased systemic inflammation, immune dysregulation, gut microbiota dysbiosis and thereby possibly influencing colorectal carcinogenesis. Periodontal-associated bacteria such as Fusobacterium, Prevotella, Bacteroides and Porphyromonas have been found in CRC tissues and in feces of CRC patients. Therefore, a deeper understanding of the association between oral and gastrointestinal bacterial profile, in addition to identifying prevalent bacteria in patients with CRC and the differences observed in ethnicity/race, may play a pivotal role in predicting incidence, prognosis, and lead to the development of new treatments. |
format | Online Article Text |
id | pubmed-8918999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-89189992022-03-21 Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences Tortora, Sofia C Bodiwala, Vimal M Quinn, Andrew Martello, Laura A Vignesh, Shivakumar World J Gastrointest Oncol Review Various studies have shown the interplay between the intestinal microbiome, environmental factors, and genetic changes in colorectal cancer (CRC) development. In this review, we highlight the various gut and oral microbiota associated with CRC and colorectal adenomas, and their proposed molecular mechanisms in relation to the processes of “the hallmarks of cancer”, and differences in microbial diversity and abundance between race/ethnicity. Patients with CRC showed increased levels of Bacteroides, Prevotella, Escherichia coli, enterotoxigenic Bacteroides fragilis, Streptococcus gallolyticus, Enterococcus faecalis, Fusobacterium nucleatum (F. nucleatum) and Clostridium difficile. Higher levels of Bacteroides have been found in African American (AA) compared to Caucasian American (CA) patients. Pro-inflammatory bacteria such as F. nucleatum and Enterobacter species were significantly higher in AAs. Also, AA patients have been shown to have decreased microbial diversity compared to CA patients. Some studies have shown that using microbiome profiles in conjunction with certain risk factors such as age, race and body mass index may help predict healthy colon vs one with adenomas or carcinomas. Periodontitis is one of the most common bacterial infections in humans and is more prevalent in Non-Hispanic-Blacks as compared to Non-Hispanic Whites. This condition causes increased systemic inflammation, immune dysregulation, gut microbiota dysbiosis and thereby possibly influencing colorectal carcinogenesis. Periodontal-associated bacteria such as Fusobacterium, Prevotella, Bacteroides and Porphyromonas have been found in CRC tissues and in feces of CRC patients. Therefore, a deeper understanding of the association between oral and gastrointestinal bacterial profile, in addition to identifying prevalent bacteria in patients with CRC and the differences observed in ethnicity/race, may play a pivotal role in predicting incidence, prognosis, and lead to the development of new treatments. Baishideng Publishing Group Inc 2022-02-15 2022-02-15 /pmc/articles/PMC8918999/ /pubmed/35317317 http://dx.doi.org/10.4251/wjgo.v14.i2.375 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Review Tortora, Sofia C Bodiwala, Vimal M Quinn, Andrew Martello, Laura A Vignesh, Shivakumar Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title | Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title_full | Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title_fullStr | Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title_full_unstemmed | Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title_short | Microbiome and colorectal carcinogenesis: Linked mechanisms and racial differences |
title_sort | microbiome and colorectal carcinogenesis: linked mechanisms and racial differences |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918999/ https://www.ncbi.nlm.nih.gov/pubmed/35317317 http://dx.doi.org/10.4251/wjgo.v14.i2.375 |
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