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Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer
The human microbiota comprises trillions of microbes, and the relationship between cancer and microbiota is very complex. The impact of fecal microbiota alterations on colorectal cancer (CRC) pathogenesis is emerging. This study analyzed changes in the microbial composition in CRC subjects with both...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477046/ https://www.ncbi.nlm.nih.gov/pubmed/34595105 http://dx.doi.org/10.3389/fonc.2021.650026 |
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author | Park, Jihye Kim, Nam-Eun Yoon, Hyuk Shin, Cheol Min Kim, Nayoung Lee, Dong Ho Park, Jae Yong Choi, Chang Hwan Kim, Jae Gyu Kim, Yoon-Keun Shin, Tae-Seop Yang, Jinho Park, Young Soo |
author_facet | Park, Jihye Kim, Nam-Eun Yoon, Hyuk Shin, Cheol Min Kim, Nayoung Lee, Dong Ho Park, Jae Yong Choi, Chang Hwan Kim, Jae Gyu Kim, Yoon-Keun Shin, Tae-Seop Yang, Jinho Park, Young Soo |
author_sort | Park, Jihye |
collection | PubMed |
description | The human microbiota comprises trillions of microbes, and the relationship between cancer and microbiota is very complex. The impact of fecal microbiota alterations on colorectal cancer (CRC) pathogenesis is emerging. This study analyzed changes in the microbial composition in CRC subjects with both fecal microbiota and gut microbe-derived extracellular vesicles (EVs). From August 2017 to August 2018, 70 CRC patients and 158 control subjects were enrolled in the study. Metagenomic profiling of fecal microbiota and gut microbe-derived EVs in stool was performed using 16S ribosomal DNA sequencing. Relative abundance, evenness, and diversity in both the gut microbiota and gut microbe-derived EVs were analyzed. Additionally, microbial composition changes according to the stage and location of CRC were analyzed. Microbial composition was significantly changed in CRC subjects compared to control subjects, with evenness and diversity significantly lower in the fecal microbiota of CRC subjects. Gut microbe-derived EVs of stool demonstrated significant differences in the microbial composition, evenness, and diversity in CRC subjects compared to the control subjects. Additionally, microbial composition, evenness, and diversity significantly changed in late CRC subjects compared to early CRC subjects with both fecal microbiota and gut microbe-derived EVs. Alistipes-derived EVs could be novel biomarkers for diagnosing CRC and predicting CRC stages. Ruminococcus 2-derived EVs significantly decreased in distal CRC subjects than in proximal CRC subjects. Gut microbe-derived EVs in CRC had a distinct microbial composition compared to the controls. Profiling of microbe-derived EVs may offer a novel biomarker for detecting and predicting CRC prognosis. |
format | Online Article Text |
id | pubmed-8477046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84770462021-09-29 Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer Park, Jihye Kim, Nam-Eun Yoon, Hyuk Shin, Cheol Min Kim, Nayoung Lee, Dong Ho Park, Jae Yong Choi, Chang Hwan Kim, Jae Gyu Kim, Yoon-Keun Shin, Tae-Seop Yang, Jinho Park, Young Soo Front Oncol Oncology The human microbiota comprises trillions of microbes, and the relationship between cancer and microbiota is very complex. The impact of fecal microbiota alterations on colorectal cancer (CRC) pathogenesis is emerging. This study analyzed changes in the microbial composition in CRC subjects with both fecal microbiota and gut microbe-derived extracellular vesicles (EVs). From August 2017 to August 2018, 70 CRC patients and 158 control subjects were enrolled in the study. Metagenomic profiling of fecal microbiota and gut microbe-derived EVs in stool was performed using 16S ribosomal DNA sequencing. Relative abundance, evenness, and diversity in both the gut microbiota and gut microbe-derived EVs were analyzed. Additionally, microbial composition changes according to the stage and location of CRC were analyzed. Microbial composition was significantly changed in CRC subjects compared to control subjects, with evenness and diversity significantly lower in the fecal microbiota of CRC subjects. Gut microbe-derived EVs of stool demonstrated significant differences in the microbial composition, evenness, and diversity in CRC subjects compared to the control subjects. Additionally, microbial composition, evenness, and diversity significantly changed in late CRC subjects compared to early CRC subjects with both fecal microbiota and gut microbe-derived EVs. Alistipes-derived EVs could be novel biomarkers for diagnosing CRC and predicting CRC stages. Ruminococcus 2-derived EVs significantly decreased in distal CRC subjects than in proximal CRC subjects. Gut microbe-derived EVs in CRC had a distinct microbial composition compared to the controls. Profiling of microbe-derived EVs may offer a novel biomarker for detecting and predicting CRC prognosis. Frontiers Media S.A. 2021-09-14 /pmc/articles/PMC8477046/ /pubmed/34595105 http://dx.doi.org/10.3389/fonc.2021.650026 Text en Copyright © 2021 Park, Kim, Yoon, Shin, Kim, Lee, Park, Choi, Kim, Kim, Shin, Yang and Park https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Park, Jihye Kim, Nam-Eun Yoon, Hyuk Shin, Cheol Min Kim, Nayoung Lee, Dong Ho Park, Jae Yong Choi, Chang Hwan Kim, Jae Gyu Kim, Yoon-Keun Shin, Tae-Seop Yang, Jinho Park, Young Soo Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title | Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title_full | Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title_fullStr | Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title_full_unstemmed | Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title_short | Fecal Microbiota and Gut Microbe-Derived Extracellular Vesicles in Colorectal Cancer |
title_sort | fecal microbiota and gut microbe-derived extracellular vesicles in colorectal cancer |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477046/ https://www.ncbi.nlm.nih.gov/pubmed/34595105 http://dx.doi.org/10.3389/fonc.2021.650026 |
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