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The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice

The human intestinal microbiota, also known as the gut microbiota, comprises more than 100 trillion organisms, mainly bacteria. This number exceeds the host body cells by a factor of ten. The gastrointestinal tract, which houses 60%–80% of the host’s immune cells, is one of the largest immune organs...

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Autores principales: Asseri, Amer H., Bakhsh, Tahani, Abuzahrah, Samah Sulaiman, Ali, Sajad, Rather, Irfan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288883/
https://www.ncbi.nlm.nih.gov/pubmed/37361202
http://dx.doi.org/10.3389/fphar.2023.1208044
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author Asseri, Amer H.
Bakhsh, Tahani
Abuzahrah, Samah Sulaiman
Ali, Sajad
Rather, Irfan A.
author_facet Asseri, Amer H.
Bakhsh, Tahani
Abuzahrah, Samah Sulaiman
Ali, Sajad
Rather, Irfan A.
author_sort Asseri, Amer H.
collection PubMed
description The human intestinal microbiota, also known as the gut microbiota, comprises more than 100 trillion organisms, mainly bacteria. This number exceeds the host body cells by a factor of ten. The gastrointestinal tract, which houses 60%–80% of the host’s immune cells, is one of the largest immune organs. It maintains systemic immune homeostasis in the face of constant bacterial challenges. The gut microbiota has evolved with the host, and its symbiotic state with the host’s gut epithelium is a testament to this co-evolution. However, certain microbial subpopulations may expand during pathological interventions, disrupting the delicate species-level microbial equilibrium and triggering inflammation and tumorigenesis. This review highlights the impact of gut microbiota dysbiosis on the development and progression of certain types of cancers and discusses the potential for developing new therapeutic strategies against cancer by manipulating the gut microbiota. By interacting with the host microbiota, we may be able to enhance the effectiveness of anticancer therapies and open new avenues for improving patient outcomes.
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spelling pubmed-102888832023-06-24 The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice Asseri, Amer H. Bakhsh, Tahani Abuzahrah, Samah Sulaiman Ali, Sajad Rather, Irfan A. Front Pharmacol Pharmacology The human intestinal microbiota, also known as the gut microbiota, comprises more than 100 trillion organisms, mainly bacteria. This number exceeds the host body cells by a factor of ten. The gastrointestinal tract, which houses 60%–80% of the host’s immune cells, is one of the largest immune organs. It maintains systemic immune homeostasis in the face of constant bacterial challenges. The gut microbiota has evolved with the host, and its symbiotic state with the host’s gut epithelium is a testament to this co-evolution. However, certain microbial subpopulations may expand during pathological interventions, disrupting the delicate species-level microbial equilibrium and triggering inflammation and tumorigenesis. This review highlights the impact of gut microbiota dysbiosis on the development and progression of certain types of cancers and discusses the potential for developing new therapeutic strategies against cancer by manipulating the gut microbiota. By interacting with the host microbiota, we may be able to enhance the effectiveness of anticancer therapies and open new avenues for improving patient outcomes. Frontiers Media S.A. 2023-06-09 /pmc/articles/PMC10288883/ /pubmed/37361202 http://dx.doi.org/10.3389/fphar.2023.1208044 Text en Copyright © 2023 Asseri, Bakhsh, Abuzahrah, Ali and Rather. 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 Pharmacology
Asseri, Amer H.
Bakhsh, Tahani
Abuzahrah, Samah Sulaiman
Ali, Sajad
Rather, Irfan A.
The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title_full The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title_fullStr The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title_full_unstemmed The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title_short The gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
title_sort gut dysbiosis-cancer axis: illuminating novel insights and implications for clinical practice
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288883/
https://www.ncbi.nlm.nih.gov/pubmed/37361202
http://dx.doi.org/10.3389/fphar.2023.1208044
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