Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.

We tested the hypothesis that changing the gut microbiota using pectic oligosaccharides (POS) or inulin (INU) differently modulates the progression of leukemia and related metabolic disorders. Mice were transplanted with Bcr-Abl-transfected proB lymphocytes mimicking leukemia and received either POS...

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Main Authors: Laure B Bindels, Audrey M Neyrinck, Nuria Salazar, Bernard Taminiau, Céline Druart, Giulio G Muccioli, Emmanuelle François, Christophe Blecker, Aurore Richel, Georges Daube, Jacques Mahillon, Clara G de los Reyes-Gavilán, Patrice D Cani, Nathalie M Delzenne
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0131009&type=printable
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author Laure B Bindels
Audrey M Neyrinck
Nuria Salazar
Bernard Taminiau
Céline Druart
Giulio G Muccioli
Emmanuelle François
Christophe Blecker
Aurore Richel
Georges Daube
Jacques Mahillon
Clara G de los Reyes-Gavilán
Patrice D Cani
Nathalie M Delzenne
author_facet Laure B Bindels
Audrey M Neyrinck
Nuria Salazar
Bernard Taminiau
Céline Druart
Giulio G Muccioli
Emmanuelle François
Christophe Blecker
Aurore Richel
Georges Daube
Jacques Mahillon
Clara G de los Reyes-Gavilán
Patrice D Cani
Nathalie M Delzenne
author_sort Laure B Bindels
collection DOAJ
description We tested the hypothesis that changing the gut microbiota using pectic oligosaccharides (POS) or inulin (INU) differently modulates the progression of leukemia and related metabolic disorders. Mice were transplanted with Bcr-Abl-transfected proB lymphocytes mimicking leukemia and received either POS or INU in their diet (5%) for 2 weeks. Combination of pyrosequencing, PCR-DGGE and qPCR analyses of the 16S rRNA gene revealed that POS decreased microbial diversity and richness of caecal microbiota whereas it increased Bifidobacterium spp., Roseburia spp. and Bacteroides spp. (affecting specifically B. dorei) to a higher extent than INU. INU supplementation increased the portal SCFA propionate and butyrate, and decreased cancer cell invasion in the liver. POS treatment did not affect hepatic cancer cell invasion, but was more efficient than INU to decrease the metabolic alterations. Indeed, POS better than INU delayed anorexia linked to cancer progression. In addition, POS treatment increased acetate in the caecal content, changed the fatty acid profile inside adipose tissue and counteracted the induction of markers controlling β-oxidation, thereby hampering fat mass loss. Non digestible carbohydrates with prebiotic properties may constitute a new nutritional strategy to modulate gut microbiota with positive consequences on cancer progression and associated cachexia.
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spelling doaj-art-52d1d31bc71c417b9c8d72f3b46fa7202025-08-20T02:34:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e013100910.1371/journal.pone.0131009Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.Laure B BindelsAudrey M NeyrinckNuria SalazarBernard TaminiauCéline DruartGiulio G MuccioliEmmanuelle FrançoisChristophe BleckerAurore RichelGeorges DaubeJacques MahillonClara G de los Reyes-GavilánPatrice D CaniNathalie M DelzenneWe tested the hypothesis that changing the gut microbiota using pectic oligosaccharides (POS) or inulin (INU) differently modulates the progression of leukemia and related metabolic disorders. Mice were transplanted with Bcr-Abl-transfected proB lymphocytes mimicking leukemia and received either POS or INU in their diet (5%) for 2 weeks. Combination of pyrosequencing, PCR-DGGE and qPCR analyses of the 16S rRNA gene revealed that POS decreased microbial diversity and richness of caecal microbiota whereas it increased Bifidobacterium spp., Roseburia spp. and Bacteroides spp. (affecting specifically B. dorei) to a higher extent than INU. INU supplementation increased the portal SCFA propionate and butyrate, and decreased cancer cell invasion in the liver. POS treatment did not affect hepatic cancer cell invasion, but was more efficient than INU to decrease the metabolic alterations. Indeed, POS better than INU delayed anorexia linked to cancer progression. In addition, POS treatment increased acetate in the caecal content, changed the fatty acid profile inside adipose tissue and counteracted the induction of markers controlling β-oxidation, thereby hampering fat mass loss. Non digestible carbohydrates with prebiotic properties may constitute a new nutritional strategy to modulate gut microbiota with positive consequences on cancer progression and associated cachexia.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0131009&type=printable
spellingShingle Laure B Bindels
Audrey M Neyrinck
Nuria Salazar
Bernard Taminiau
Céline Druart
Giulio G Muccioli
Emmanuelle François
Christophe Blecker
Aurore Richel
Georges Daube
Jacques Mahillon
Clara G de los Reyes-Gavilán
Patrice D Cani
Nathalie M Delzenne
Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
PLoS ONE
title Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
title_full Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
title_fullStr Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
title_full_unstemmed Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
title_short Non Digestible Oligosaccharides Modulate the Gut Microbiota to Control the Development of Leukemia and Associated Cachexia in Mice.
title_sort non digestible oligosaccharides modulate the gut microbiota to control the development of leukemia and associated cachexia in mice
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0131009&type=printable
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