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Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer

BACKGROUND: Gut microbiota plays a significant role in the colorectal cancer (CRC) process. Ectopic colonization of multiple oral bacteria is reportedly associated with CRC pathogenesis and progression, but the details remain unclear. METHODS: We enrolled a cohort of 50 CRC patients and 52 healthy c...

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Autores principales: Zhang, Hongze, Jin, Kai, Xiong, Kunlong, Jing, Wenwen, Pang, Zhen, Feng, Meng, Cheng, Xunjia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417192/
https://www.ncbi.nlm.nih.gov/pubmed/37260140
http://dx.doi.org/10.1002/cam4.6194
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author Zhang, Hongze
Jin, Kai
Xiong, Kunlong
Jing, Wenwen
Pang, Zhen
Feng, Meng
Cheng, Xunjia
author_facet Zhang, Hongze
Jin, Kai
Xiong, Kunlong
Jing, Wenwen
Pang, Zhen
Feng, Meng
Cheng, Xunjia
author_sort Zhang, Hongze
collection PubMed
description BACKGROUND: Gut microbiota plays a significant role in the colorectal cancer (CRC) process. Ectopic colonization of multiple oral bacteria is reportedly associated with CRC pathogenesis and progression, but the details remain unclear. METHODS: We enrolled a cohort of 50 CRC patients and 52 healthy controls from an East China population. Taxonomic and functional analysis of the fecal microbiota were performed using 16S rDNA (50 + 52 samples) and shotgun metagenomic sequencing (8 + 6 samples), respectively, with particular attention paid to gut‐colonized oral bacteria. RESULTS AND CONCLUSIONS: The results showed more detected bacterial species but lower species evenness within the samples from CRC patients. To determine the specific bacteria enriched in each group, we analyzed their possible protective, carcinogenic, or opportunistic roles in the CRC process. Among the ectopic oral bacteria, we observed a significant increase in the abundance of Fusobacterium and decreased abundance of Prevotella and Ruminococcus in the CRC group. Main differences in the functional composition of these two groups were related to energy metabolism and biosynthesis, especially the glycolytic pathway. Furthermore, we validated the colonization of Fusobacterium nucleatum subsp. animalis within CRC tissues and studied its impact on the host intestinal epithelium and tumor cells. With high selectivity for cancerous tissues, this subspecies promoted CRC cell proliferation and induced potential DNA damage.
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spelling pubmed-104171922023-08-12 Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer Zhang, Hongze Jin, Kai Xiong, Kunlong Jing, Wenwen Pang, Zhen Feng, Meng Cheng, Xunjia Cancer Med Research Articles BACKGROUND: Gut microbiota plays a significant role in the colorectal cancer (CRC) process. Ectopic colonization of multiple oral bacteria is reportedly associated with CRC pathogenesis and progression, but the details remain unclear. METHODS: We enrolled a cohort of 50 CRC patients and 52 healthy controls from an East China population. Taxonomic and functional analysis of the fecal microbiota were performed using 16S rDNA (50 + 52 samples) and shotgun metagenomic sequencing (8 + 6 samples), respectively, with particular attention paid to gut‐colonized oral bacteria. RESULTS AND CONCLUSIONS: The results showed more detected bacterial species but lower species evenness within the samples from CRC patients. To determine the specific bacteria enriched in each group, we analyzed their possible protective, carcinogenic, or opportunistic roles in the CRC process. Among the ectopic oral bacteria, we observed a significant increase in the abundance of Fusobacterium and decreased abundance of Prevotella and Ruminococcus in the CRC group. Main differences in the functional composition of these two groups were related to energy metabolism and biosynthesis, especially the glycolytic pathway. Furthermore, we validated the colonization of Fusobacterium nucleatum subsp. animalis within CRC tissues and studied its impact on the host intestinal epithelium and tumor cells. With high selectivity for cancerous tissues, this subspecies promoted CRC cell proliferation and induced potential DNA damage. John Wiley and Sons Inc. 2023-06-01 /pmc/articles/PMC10417192/ /pubmed/37260140 http://dx.doi.org/10.1002/cam4.6194 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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
Zhang, Hongze
Jin, Kai
Xiong, Kunlong
Jing, Wenwen
Pang, Zhen
Feng, Meng
Cheng, Xunjia
Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title_full Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title_fullStr Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title_full_unstemmed Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title_short Disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
title_sort disease‐associated gut microbiome and critical metabolomic alterations in patients with colorectal cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417192/
https://www.ncbi.nlm.nih.gov/pubmed/37260140
http://dx.doi.org/10.1002/cam4.6194
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