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Influence of the microbiota on epigenetics in colorectal cancer

Colorectal cancer is one of the most common malignancies and is the second leading cause of cancer death worldwide. Generally, there are three categories of colorectal cancer development mechanism—genetic, epigenetic and aberrant immunological signaling pathways—all of which may be initiated by an i...

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Autores principales: Sun, Danfeng, Chen, Yingxuan, Fang, Jing-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291637/
https://www.ncbi.nlm.nih.gov/pubmed/34691992
http://dx.doi.org/10.1093/nsr/nwy160
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author Sun, Danfeng
Chen, Yingxuan
Fang, Jing-Yuan
author_facet Sun, Danfeng
Chen, Yingxuan
Fang, Jing-Yuan
author_sort Sun, Danfeng
collection PubMed
description Colorectal cancer is one of the most common malignancies and is the second leading cause of cancer death worldwide. Generally, there are three categories of colorectal cancer development mechanism—genetic, epigenetic and aberrant immunological signaling pathways—all of which may be initiated by an imbalanced gut microbiota. Epigenetic modifications enable host cells to change gene expression without modifying the gene sequence. The microbiota can interact with the host genome dynamically through the interface presented by epigenetic modifications. In particular, bacterially derived short-chain fatty acids have been identified as one clear link in the interaction of the microbiota with host epigenetic pathways. This review discusses recent findings relating to the cross talk between the microbiota and epigenetic modifications in colorectal cancer.
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spelling pubmed-82916372021-10-21 Influence of the microbiota on epigenetics in colorectal cancer Sun, Danfeng Chen, Yingxuan Fang, Jing-Yuan Natl Sci Rev Special Topic: Chemistry and Molecular Medicine Colorectal cancer is one of the most common malignancies and is the second leading cause of cancer death worldwide. Generally, there are three categories of colorectal cancer development mechanism—genetic, epigenetic and aberrant immunological signaling pathways—all of which may be initiated by an imbalanced gut microbiota. Epigenetic modifications enable host cells to change gene expression without modifying the gene sequence. The microbiota can interact with the host genome dynamically through the interface presented by epigenetic modifications. In particular, bacterially derived short-chain fatty acids have been identified as one clear link in the interaction of the microbiota with host epigenetic pathways. This review discusses recent findings relating to the cross talk between the microbiota and epigenetic modifications in colorectal cancer. Oxford University Press 2019-11 2018-12-22 /pmc/articles/PMC8291637/ /pubmed/34691992 http://dx.doi.org/10.1093/nsr/nwy160 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Topic: Chemistry and Molecular Medicine
Sun, Danfeng
Chen, Yingxuan
Fang, Jing-Yuan
Influence of the microbiota on epigenetics in colorectal cancer
title Influence of the microbiota on epigenetics in colorectal cancer
title_full Influence of the microbiota on epigenetics in colorectal cancer
title_fullStr Influence of the microbiota on epigenetics in colorectal cancer
title_full_unstemmed Influence of the microbiota on epigenetics in colorectal cancer
title_short Influence of the microbiota on epigenetics in colorectal cancer
title_sort influence of the microbiota on epigenetics in colorectal cancer
topic Special Topic: Chemistry and Molecular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8291637/
https://www.ncbi.nlm.nih.gov/pubmed/34691992
http://dx.doi.org/10.1093/nsr/nwy160
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