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Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development

In recent years, the number of studies investigating the impact of the gut microbiome in colorectal cancer (CRC) has risen sharply. As a result, we now know that various microbes (and microbial communities) are found more frequently in the stool and mucosa of individuals with CRC than healthy contro...

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Autores principales: Allen, Jawara, Sears, Cynthia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388476/
https://www.ncbi.nlm.nih.gov/pubmed/30803449
http://dx.doi.org/10.1186/s13073-019-0621-2
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author Allen, Jawara
Sears, Cynthia L.
author_facet Allen, Jawara
Sears, Cynthia L.
author_sort Allen, Jawara
collection PubMed
description In recent years, the number of studies investigating the impact of the gut microbiome in colorectal cancer (CRC) has risen sharply. As a result, we now know that various microbes (and microbial communities) are found more frequently in the stool and mucosa of individuals with CRC than healthy controls, including in the primary tumors themselves, and even in distant metastases. We also know that these microbes induce tumors in various mouse models, but we know little about how they impact colon epithelial cells (CECs) directly, or about how these interactions might lead to modifications at the genetic and epigenetic levels that trigger and propagate tumor growth. Rates of CRC are increasing in younger individuals, and CRC remains the second most frequent cause of cancer-related deaths globally. Hence, a more in-depth understanding of the role that gut microbes play in CRC is needed. Here, we review recent advances in understanding the impact of gut microbes on the genome and epigenome of CECs, as it relates to CRC. Overall, numerous studies in the past few years have definitively shown that gut microbes exert distinct impacts on DNA damage, DNA methylation, chromatin structure and non-coding RNA expression in CECs. Some of the genes and pathways that are altered by gut microbes relate to CRC development, particularly those involved in cell proliferation and WNT signaling. We need to implement more standardized analysis strategies, collate data from multiple studies, and utilize CRC mouse models to better assess these effects, understand their functional relevance, and leverage this information to improve patient care.
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spelling pubmed-63884762019-03-19 Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development Allen, Jawara Sears, Cynthia L. Genome Med Review In recent years, the number of studies investigating the impact of the gut microbiome in colorectal cancer (CRC) has risen sharply. As a result, we now know that various microbes (and microbial communities) are found more frequently in the stool and mucosa of individuals with CRC than healthy controls, including in the primary tumors themselves, and even in distant metastases. We also know that these microbes induce tumors in various mouse models, but we know little about how they impact colon epithelial cells (CECs) directly, or about how these interactions might lead to modifications at the genetic and epigenetic levels that trigger and propagate tumor growth. Rates of CRC are increasing in younger individuals, and CRC remains the second most frequent cause of cancer-related deaths globally. Hence, a more in-depth understanding of the role that gut microbes play in CRC is needed. Here, we review recent advances in understanding the impact of gut microbes on the genome and epigenome of CECs, as it relates to CRC. Overall, numerous studies in the past few years have definitively shown that gut microbes exert distinct impacts on DNA damage, DNA methylation, chromatin structure and non-coding RNA expression in CECs. Some of the genes and pathways that are altered by gut microbes relate to CRC development, particularly those involved in cell proliferation and WNT signaling. We need to implement more standardized analysis strategies, collate data from multiple studies, and utilize CRC mouse models to better assess these effects, understand their functional relevance, and leverage this information to improve patient care. BioMed Central 2019-02-25 /pmc/articles/PMC6388476/ /pubmed/30803449 http://dx.doi.org/10.1186/s13073-019-0621-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Allen, Jawara
Sears, Cynthia L.
Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title_full Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title_fullStr Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title_full_unstemmed Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title_short Impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
title_sort impact of the gut microbiome on the genome and epigenome of colon epithelial cells: contributions to colorectal cancer development
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388476/
https://www.ncbi.nlm.nih.gov/pubmed/30803449
http://dx.doi.org/10.1186/s13073-019-0621-2
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