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Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis

Intestinal microbiota play a significant role in nutrient metabolism, modulation of the immune system, obesity, and possibly in carcinogenesis, although the underlying mechanisms resulting in disease or impacts on longevity caused by different intestinal microbiota are mostly unknown. Herein we use...

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Autores principales: Cheema, Amrita K., Maier, Irene, Dowdy, Tyrone, Wang, Yiwen, Singh, Rajbir, Ruegger, Paul M., Borneman, James, Fornace, Albert J., Schiestl, Robert H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830457/
https://www.ncbi.nlm.nih.gov/pubmed/27073845
http://dx.doi.org/10.1371/journal.pone.0151190
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author Cheema, Amrita K.
Maier, Irene
Dowdy, Tyrone
Wang, Yiwen
Singh, Rajbir
Ruegger, Paul M.
Borneman, James
Fornace, Albert J.
Schiestl, Robert H.
author_facet Cheema, Amrita K.
Maier, Irene
Dowdy, Tyrone
Wang, Yiwen
Singh, Rajbir
Ruegger, Paul M.
Borneman, James
Fornace, Albert J.
Schiestl, Robert H.
author_sort Cheema, Amrita K.
collection PubMed
description Intestinal microbiota play a significant role in nutrient metabolism, modulation of the immune system, obesity, and possibly in carcinogenesis, although the underlying mechanisms resulting in disease or impacts on longevity caused by different intestinal microbiota are mostly unknown. Herein we use isogenic Atm-deficient and wild type mice as models to interrogate changes in the metabolic profiles of urine and feces of these mice, which are differing in their intestinal microbiota. Using high resolution mass spectrometry approach we show that the composition of intestinal microbiota modulates specific metabolic perturbations resulting in a possible alleviation of a glycolytic phenotype. Metabolites including 3-methylbutyrolactone, kyneurenic acid and 3-methyladenine known to be onco-protective are elevated in Atm-deficient and wild type mice with restricted intestinal microbiota. Thus our approach has broad applicability to study the direct influence of gut microbiome on host metabolism and resultant phenotype. These results for the first time suggest a possible correlation of metabolic alterations and carcinogenesis, modulated by intestinal microbiota in A-T mice.
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spelling pubmed-48304572016-04-22 Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis Cheema, Amrita K. Maier, Irene Dowdy, Tyrone Wang, Yiwen Singh, Rajbir Ruegger, Paul M. Borneman, James Fornace, Albert J. Schiestl, Robert H. PLoS One Research Article Intestinal microbiota play a significant role in nutrient metabolism, modulation of the immune system, obesity, and possibly in carcinogenesis, although the underlying mechanisms resulting in disease or impacts on longevity caused by different intestinal microbiota are mostly unknown. Herein we use isogenic Atm-deficient and wild type mice as models to interrogate changes in the metabolic profiles of urine and feces of these mice, which are differing in their intestinal microbiota. Using high resolution mass spectrometry approach we show that the composition of intestinal microbiota modulates specific metabolic perturbations resulting in a possible alleviation of a glycolytic phenotype. Metabolites including 3-methylbutyrolactone, kyneurenic acid and 3-methyladenine known to be onco-protective are elevated in Atm-deficient and wild type mice with restricted intestinal microbiota. Thus our approach has broad applicability to study the direct influence of gut microbiome on host metabolism and resultant phenotype. These results for the first time suggest a possible correlation of metabolic alterations and carcinogenesis, modulated by intestinal microbiota in A-T mice. Public Library of Science 2016-04-13 /pmc/articles/PMC4830457/ /pubmed/27073845 http://dx.doi.org/10.1371/journal.pone.0151190 Text en © 2016 Cheema et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cheema, Amrita K.
Maier, Irene
Dowdy, Tyrone
Wang, Yiwen
Singh, Rajbir
Ruegger, Paul M.
Borneman, James
Fornace, Albert J.
Schiestl, Robert H.
Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title_full Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title_fullStr Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title_full_unstemmed Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title_short Chemopreventive Metabolites Are Correlated with a Change in Intestinal Microbiota Measured in A-T Mice and Decreased Carcinogenesis
title_sort chemopreventive metabolites are correlated with a change in intestinal microbiota measured in a-t mice and decreased carcinogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830457/
https://www.ncbi.nlm.nih.gov/pubmed/27073845
http://dx.doi.org/10.1371/journal.pone.0151190
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