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Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study
BACKGROUND: Colorectal cancer (CRC) is a common malignant gastrointestinal tumor. In China, CRC is the 5th most commonly diagnosed cancer. The vast majority of CRC cases are sporadic and evolve with the adenoma-carcinoma sequence. There is mounting evidence indicating that gut microbiota and inflamm...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114884/ https://www.ncbi.nlm.nih.gov/pubmed/30157754 http://dx.doi.org/10.1186/s12866-018-1232-6 |
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author | Zhang, Yongzhen Yu, Xin Yu, Enda Wang, Na Cai, Quancai Shuai, Qun Yan, Feihu Jiang, Lufang Wang, Hexing Liu, Jianxiang Chen, Yue Li, Zhaoshen Jiang, Qingwu |
author_facet | Zhang, Yongzhen Yu, Xin Yu, Enda Wang, Na Cai, Quancai Shuai, Qun Yan, Feihu Jiang, Lufang Wang, Hexing Liu, Jianxiang Chen, Yue Li, Zhaoshen Jiang, Qingwu |
author_sort | Zhang, Yongzhen |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is a common malignant gastrointestinal tumor. In China, CRC is the 5th most commonly diagnosed cancer. The vast majority of CRC cases are sporadic and evolve with the adenoma-carcinoma sequence. There is mounting evidence indicating that gut microbiota and inflammation play important roles in the development of CRC although study results are not entirely consistent. In the current study, we investigated the changes in the CRC-associated bacteria and plasma inflammatory factors and their relationships based on data from a case-control study of Han Chinese. We included 130 initially diagnosed CRC patients, 88 advanced colorectal adenoma patients (A-CRA), 62 patients with benign intestinal polyps and 130 controls. RESULTS: Fecal microbiota composition was obtained using 16S ribosomal DNA (16S rDNA) sequencing. PCOA analysis showed structural differences in microbiota among the four study groups (P = 0.001, Unweighted Unifrac). Twenty-four CRC-associated bacteria were selected by a two-step statistical method and significant correlations were observed within these microbes. CRC-associated bacteria were found to change with the degree of malignancy. Plasma C-reactive protein (CRP) and soluble tumor necrosis factor II (sTNFR-II) displayed significant differences among the four study groups and increased with adenoma-carcinoma sequence. The correlations of CRP and sTNFR-II with several CRC-associated microbes were also explored. CONCLUSIONS: CRC-associated species and plasma inflammatory factors tended to change along the adenoma-carcinoma sequence. Several CRC-associated bacteria were correlated with CRP and sTNFR-II. It is likely that gut microbiome and inflammation gradually form a microenvironment that is associated with CRC development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1232-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6114884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61148842018-09-04 Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study Zhang, Yongzhen Yu, Xin Yu, Enda Wang, Na Cai, Quancai Shuai, Qun Yan, Feihu Jiang, Lufang Wang, Hexing Liu, Jianxiang Chen, Yue Li, Zhaoshen Jiang, Qingwu BMC Microbiol Research Article BACKGROUND: Colorectal cancer (CRC) is a common malignant gastrointestinal tumor. In China, CRC is the 5th most commonly diagnosed cancer. The vast majority of CRC cases are sporadic and evolve with the adenoma-carcinoma sequence. There is mounting evidence indicating that gut microbiota and inflammation play important roles in the development of CRC although study results are not entirely consistent. In the current study, we investigated the changes in the CRC-associated bacteria and plasma inflammatory factors and their relationships based on data from a case-control study of Han Chinese. We included 130 initially diagnosed CRC patients, 88 advanced colorectal adenoma patients (A-CRA), 62 patients with benign intestinal polyps and 130 controls. RESULTS: Fecal microbiota composition was obtained using 16S ribosomal DNA (16S rDNA) sequencing. PCOA analysis showed structural differences in microbiota among the four study groups (P = 0.001, Unweighted Unifrac). Twenty-four CRC-associated bacteria were selected by a two-step statistical method and significant correlations were observed within these microbes. CRC-associated bacteria were found to change with the degree of malignancy. Plasma C-reactive protein (CRP) and soluble tumor necrosis factor II (sTNFR-II) displayed significant differences among the four study groups and increased with adenoma-carcinoma sequence. The correlations of CRP and sTNFR-II with several CRC-associated microbes were also explored. CONCLUSIONS: CRC-associated species and plasma inflammatory factors tended to change along the adenoma-carcinoma sequence. Several CRC-associated bacteria were correlated with CRP and sTNFR-II. It is likely that gut microbiome and inflammation gradually form a microenvironment that is associated with CRC development. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1232-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-29 /pmc/articles/PMC6114884/ /pubmed/30157754 http://dx.doi.org/10.1186/s12866-018-1232-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhang, Yongzhen Yu, Xin Yu, Enda Wang, Na Cai, Quancai Shuai, Qun Yan, Feihu Jiang, Lufang Wang, Hexing Liu, Jianxiang Chen, Yue Li, Zhaoshen Jiang, Qingwu Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title | Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title_full | Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title_fullStr | Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title_full_unstemmed | Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title_short | Changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
title_sort | changes in gut microbiota and plasma inflammatory factors across the stages of colorectal tumorigenesis: a case-control study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114884/ https://www.ncbi.nlm.nih.gov/pubmed/30157754 http://dx.doi.org/10.1186/s12866-018-1232-6 |
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