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Enteric Bacteria and Cancer Stem Cells

Intestinal bacteria can contribute to cell proliferation and cancer development, particularly in chronic infectious diseases in which bacteria and/or bacterial components might interfere with cell function. The number of microbial cells within the gut lumen is estimated to be 100 trillion, which is...

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Detalles Bibliográficos
Autor principal: Sun, Jun
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033586/
https://www.ncbi.nlm.nih.gov/pubmed/21297903
http://dx.doi.org/10.3390/cancers3010285
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author Sun, Jun
author_facet Sun, Jun
author_sort Sun, Jun
collection PubMed
description Intestinal bacteria can contribute to cell proliferation and cancer development, particularly in chronic infectious diseases in which bacteria and/or bacterial components might interfere with cell function. The number of microbial cells within the gut lumen is estimated to be 100 trillion, which is about 10-times larger than the number of eukaryotic cells in the human body. Because of the complexity of the gut flora, identifying the specific microbial agents related to human diseases remains challenging. Recent studies have demonstrated that the stemness of colon cancer cells is, in part, orchestrated by the microenvironment and is defined by high Wnt activity. In this review article, we will discuss recent progress with respect to intestinal stem cells, cancer stem cells, and the molecular mechanisms of enteric bacteria in the activation of the Wnt pathway. We will also discuss the roles of other pathways, including JAK-STAT, JNK, and Notch, in regulating stem cell niches during bacterial infections using Drosophila models. Insights gained from understanding how host-bacterial interaction during inflammation and cancer may serve as a paradigm for understanding the nature of self-renewal signals.
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spelling pubmed-30335862011-02-04 Enteric Bacteria and Cancer Stem Cells Sun, Jun Cancers (Basel) Review Intestinal bacteria can contribute to cell proliferation and cancer development, particularly in chronic infectious diseases in which bacteria and/or bacterial components might interfere with cell function. The number of microbial cells within the gut lumen is estimated to be 100 trillion, which is about 10-times larger than the number of eukaryotic cells in the human body. Because of the complexity of the gut flora, identifying the specific microbial agents related to human diseases remains challenging. Recent studies have demonstrated that the stemness of colon cancer cells is, in part, orchestrated by the microenvironment and is defined by high Wnt activity. In this review article, we will discuss recent progress with respect to intestinal stem cells, cancer stem cells, and the molecular mechanisms of enteric bacteria in the activation of the Wnt pathway. We will also discuss the roles of other pathways, including JAK-STAT, JNK, and Notch, in regulating stem cell niches during bacterial infections using Drosophila models. Insights gained from understanding how host-bacterial interaction during inflammation and cancer may serve as a paradigm for understanding the nature of self-renewal signals. Molecular Diversity Preservation International (MDPI) 2011-01-14 /pmc/articles/PMC3033586/ /pubmed/21297903 http://dx.doi.org/10.3390/cancers3010285 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Sun, Jun
Enteric Bacteria and Cancer Stem Cells
title Enteric Bacteria and Cancer Stem Cells
title_full Enteric Bacteria and Cancer Stem Cells
title_fullStr Enteric Bacteria and Cancer Stem Cells
title_full_unstemmed Enteric Bacteria and Cancer Stem Cells
title_short Enteric Bacteria and Cancer Stem Cells
title_sort enteric bacteria and cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033586/
https://www.ncbi.nlm.nih.gov/pubmed/21297903
http://dx.doi.org/10.3390/cancers3010285
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