Microbial dysbiosis in colorectal cancer (CRC) patients.

<h4>Unlabelled</h4>The composition of the human intestinal microbiota is linked to health status. The aim was to analyze the microbiota of normal and colon cancer patients in order to establish cancer-related dysbiosis.<h4>Patients and methods</h4>Stool bacterial DNA was extr...

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Autores principales: Iradj Sobhani, Julien Tap, Françoise Roudot-Thoraval, Jean P Roperch, Sophie Letulle, Philippe Langella, Gérard Corthier, Jeanne Tran Van Nhieu, Jean P Furet
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Publicado: Public Library of Science (PLoS) 2011
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spelling oai:doaj.org-article:df92053d476b440095f4ffd4da31c1ca2021-11-18T06:59:48ZMicrobial dysbiosis in colorectal cancer (CRC) patients.1932-620310.1371/journal.pone.0016393https://doaj.org/article/df92053d476b440095f4ffd4da31c1ca2011-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21297998/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Unlabelled</h4>The composition of the human intestinal microbiota is linked to health status. The aim was to analyze the microbiota of normal and colon cancer patients in order to establish cancer-related dysbiosis.<h4>Patients and methods</h4>Stool bacterial DNA was extracted prior to colonoscopy from 179 patients: 60 with colorectal cancer, and 119 with normal colonoscopy. Bacterial genes obtained by pyrosequencing of 12 stool samples (6 Normal and 6 Cancer) were subjected to a validated Principal Component Analysis (PCA) test. The dominant and subdominant bacterial population (C. leptum, C. coccoides, Bacteroides/Prevotella, Lactobacillus/Leuconostoc/Pediococcus groups, Bifidobacterium genus, and E. coli, and Faecalibacterium prausnitzii species) were quantified in all individuals using qPCR and specific IL17 producer cells in the intestinal mucosa were characterized using immunohistochemistry.<h4>Findings</h4>Pyrosequencing (Minimal sequence 200 nucleotide reads) revealed 80% of all sequences could be assigned to a total of 819 taxa based on default parameter of Classifier software. The phylogenetic core in Cancer individuals was different from that in Normal individuals according to the PCA analysis, with trends towards differences in the dominant and subdominant families of bacteria. Consequently, All-bacteria [log(10) (bacteria/g of stool)] in Normal, and Cancer individuals were similar [11.88±0.35, and 11.80±0.56, respectively, (P = 0.16)], according to qPCR values whereas among all dominant and subdominant species only those of Bacteroides/Prevotella were higher (All bacteria-specific bacterium; P = 0.009) in Cancer (-1.04±0.55) than in Normal (-1.40±0.83) individuals. IL17 immunoreactive cells were significantly expressed more in the normal mucosa of cancer patients than in those with normal colonoscopy.<h4>Conclusion</h4>This is the first large series to demonstrate a composition change in the microbiota of colon cancer patients with possible impact on mucosal immune response. These data open new filed for mass screening and pathophysiology investigations.Iradj SobhaniJulien TapFrançoise Roudot-ThoravalJean P RoperchSophie LetullePhilippe LangellaGérard CorthierJeanne Tran Van NhieuJean P FuretPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 6, Iss 1, p e16393 (2011)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Iradj Sobhani
Julien Tap
Françoise Roudot-Thoraval
Jean P Roperch
Sophie Letulle
Philippe Langella
Gérard Corthier
Jeanne Tran Van Nhieu
Jean P Furet
Microbial dysbiosis in colorectal cancer (CRC) patients.
description <h4>Unlabelled</h4>The composition of the human intestinal microbiota is linked to health status. The aim was to analyze the microbiota of normal and colon cancer patients in order to establish cancer-related dysbiosis.<h4>Patients and methods</h4>Stool bacterial DNA was extracted prior to colonoscopy from 179 patients: 60 with colorectal cancer, and 119 with normal colonoscopy. Bacterial genes obtained by pyrosequencing of 12 stool samples (6 Normal and 6 Cancer) were subjected to a validated Principal Component Analysis (PCA) test. The dominant and subdominant bacterial population (C. leptum, C. coccoides, Bacteroides/Prevotella, Lactobacillus/Leuconostoc/Pediococcus groups, Bifidobacterium genus, and E. coli, and Faecalibacterium prausnitzii species) were quantified in all individuals using qPCR and specific IL17 producer cells in the intestinal mucosa were characterized using immunohistochemistry.<h4>Findings</h4>Pyrosequencing (Minimal sequence 200 nucleotide reads) revealed 80% of all sequences could be assigned to a total of 819 taxa based on default parameter of Classifier software. The phylogenetic core in Cancer individuals was different from that in Normal individuals according to the PCA analysis, with trends towards differences in the dominant and subdominant families of bacteria. Consequently, All-bacteria [log(10) (bacteria/g of stool)] in Normal, and Cancer individuals were similar [11.88±0.35, and 11.80±0.56, respectively, (P = 0.16)], according to qPCR values whereas among all dominant and subdominant species only those of Bacteroides/Prevotella were higher (All bacteria-specific bacterium; P = 0.009) in Cancer (-1.04±0.55) than in Normal (-1.40±0.83) individuals. IL17 immunoreactive cells were significantly expressed more in the normal mucosa of cancer patients than in those with normal colonoscopy.<h4>Conclusion</h4>This is the first large series to demonstrate a composition change in the microbiota of colon cancer patients with possible impact on mucosal immune response. These data open new filed for mass screening and pathophysiology investigations.
format article
author Iradj Sobhani
Julien Tap
Françoise Roudot-Thoraval
Jean P Roperch
Sophie Letulle
Philippe Langella
Gérard Corthier
Jeanne Tran Van Nhieu
Jean P Furet
author_facet Iradj Sobhani
Julien Tap
Françoise Roudot-Thoraval
Jean P Roperch
Sophie Letulle
Philippe Langella
Gérard Corthier
Jeanne Tran Van Nhieu
Jean P Furet
author_sort Iradj Sobhani
title Microbial dysbiosis in colorectal cancer (CRC) patients.
title_short Microbial dysbiosis in colorectal cancer (CRC) patients.
title_full Microbial dysbiosis in colorectal cancer (CRC) patients.
title_fullStr Microbial dysbiosis in colorectal cancer (CRC) patients.
title_full_unstemmed Microbial dysbiosis in colorectal cancer (CRC) patients.
title_sort microbial dysbiosis in colorectal cancer (crc) patients.
publisher Public Library of Science (PLoS)
publishDate 2011
url https://doaj.org/article/df92053d476b440095f4ffd4da31c1ca
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