Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
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
_version_ 1783351279258435584
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
work_keys_str_mv AT zhangyongzhen changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT yuxin changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT yuenda changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT wangna changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT caiquancai changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT shuaiqun changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT yanfeihu changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT jianglufang changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT wanghexing changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT liujianxiang changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT chenyue changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT lizhaoshen changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy
AT jiangqingwu changesingutmicrobiotaandplasmainflammatoryfactorsacrossthestagesofcolorectaltumorigenesisacasecontrolstudy