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Gut microbiota in patients after surgical treatment for colorectal cancer

Colorectal cancer (CRC) is a common disease worldwide that is strongly associated with the gut microbiota. However, little is known regarding the gut microbiota after surgical treatment. 16S rRNA gene sequencing was used to evaluate differences in gut microbiota among colorectal adenoma patients, CR...

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Autores principales: Jin, Ye, Liu, Yang, Zhao, Lei, Zhao, Fuya, Feng, Jing, Li, Shengda, Chen, Huinan, Sun, Jiayu, Zhu, Biqiang, Geng, Rui, Wei, Yunwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379540/
https://www.ncbi.nlm.nih.gov/pubmed/30548192
http://dx.doi.org/10.1111/1462-2920.14498
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author Jin, Ye
Liu, Yang
Zhao, Lei
Zhao, Fuya
Feng, Jing
Li, Shengda
Chen, Huinan
Sun, Jiayu
Zhu, Biqiang
Geng, Rui
Wei, Yunwei
author_facet Jin, Ye
Liu, Yang
Zhao, Lei
Zhao, Fuya
Feng, Jing
Li, Shengda
Chen, Huinan
Sun, Jiayu
Zhu, Biqiang
Geng, Rui
Wei, Yunwei
author_sort Jin, Ye
collection PubMed
description Colorectal cancer (CRC) is a common disease worldwide that is strongly associated with the gut microbiota. However, little is known regarding the gut microbiota after surgical treatment. 16S rRNA gene sequencing was used to evaluate differences in gut microbiota among colorectal adenoma patients, CRC patients, CRC postoperative patients and healthy controls by comparing gut microbiota diversity, overall composition and taxonomic signature abundance. The gut microbiota of CRC patients, adenoma patients and healthy controls developed in accordance with the adenoma‐carcinoma sequence, with impressive shifts in the gut microbiota before or during the development of CRC. The gut microbiota of postoperative patients and CRC patients differed significantly. Subdividing CRC postoperative patients according to the presence or absence of newly developed adenoma which based on the colonoscopy findings revealed that the gut microbiota of newly developed adenoma patients differed significantly from that of clean intestine patients and was more similar to the gut microbiota of carcinoma patients than to the gut microbiota of healthy controls. The alterations of the gut microbiota between the two groups of postoperative patients corresponded to CRC prognosis. More importantly, we used the different gut microbiota as biomarkers to distinguish postoperative patients with or without newly developed adenoma, achieving an AUC value of 0.72. These insights on the changes in the gut microbiota of CRC patients after surgical treatment may allow the use of the microbiota as non‐invasive biomarkers for the diagnosis of newly developed adenomas and to help prevent cancer recurrence in postoperative patients.
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spelling pubmed-73795402020-07-24 Gut microbiota in patients after surgical treatment for colorectal cancer Jin, Ye Liu, Yang Zhao, Lei Zhao, Fuya Feng, Jing Li, Shengda Chen, Huinan Sun, Jiayu Zhu, Biqiang Geng, Rui Wei, Yunwei Environ Microbiol Research Articles Colorectal cancer (CRC) is a common disease worldwide that is strongly associated with the gut microbiota. However, little is known regarding the gut microbiota after surgical treatment. 16S rRNA gene sequencing was used to evaluate differences in gut microbiota among colorectal adenoma patients, CRC patients, CRC postoperative patients and healthy controls by comparing gut microbiota diversity, overall composition and taxonomic signature abundance. The gut microbiota of CRC patients, adenoma patients and healthy controls developed in accordance with the adenoma‐carcinoma sequence, with impressive shifts in the gut microbiota before or during the development of CRC. The gut microbiota of postoperative patients and CRC patients differed significantly. Subdividing CRC postoperative patients according to the presence or absence of newly developed adenoma which based on the colonoscopy findings revealed that the gut microbiota of newly developed adenoma patients differed significantly from that of clean intestine patients and was more similar to the gut microbiota of carcinoma patients than to the gut microbiota of healthy controls. The alterations of the gut microbiota between the two groups of postoperative patients corresponded to CRC prognosis. More importantly, we used the different gut microbiota as biomarkers to distinguish postoperative patients with or without newly developed adenoma, achieving an AUC value of 0.72. These insights on the changes in the gut microbiota of CRC patients after surgical treatment may allow the use of the microbiota as non‐invasive biomarkers for the diagnosis of newly developed adenomas and to help prevent cancer recurrence in postoperative patients. John Wiley & Sons, Inc. 2018-12-19 2019-02 /pmc/articles/PMC7379540/ /pubmed/30548192 http://dx.doi.org/10.1111/1462-2920.14498 Text en © 2018 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Jin, Ye
Liu, Yang
Zhao, Lei
Zhao, Fuya
Feng, Jing
Li, Shengda
Chen, Huinan
Sun, Jiayu
Zhu, Biqiang
Geng, Rui
Wei, Yunwei
Gut microbiota in patients after surgical treatment for colorectal cancer
title Gut microbiota in patients after surgical treatment for colorectal cancer
title_full Gut microbiota in patients after surgical treatment for colorectal cancer
title_fullStr Gut microbiota in patients after surgical treatment for colorectal cancer
title_full_unstemmed Gut microbiota in patients after surgical treatment for colorectal cancer
title_short Gut microbiota in patients after surgical treatment for colorectal cancer
title_sort gut microbiota in patients after surgical treatment for colorectal cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379540/
https://www.ncbi.nlm.nih.gov/pubmed/30548192
http://dx.doi.org/10.1111/1462-2920.14498
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