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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
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.
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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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