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Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing

BACKGROUND: The microbiome has been implicated in the initiation and progression of colorectal cancer (CRC) in cross-sectional studies. However, there is a lack of studies using prospectively collected samples. METHODS: From the Norwegian Colorectal Cancer Prevention (NORCCAP) trial, we analyzed 144...

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Autores principales: Bucher-Johannessen, Cecilie, Birkeland, Einar Elvbakken, Vinberg, Elina, Bemanian, Vahid, Hoff, Geir, Berstad, Paula, Rounge, Trine B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172651/
https://www.ncbi.nlm.nih.gov/pubmed/37182146
http://dx.doi.org/10.3389/fonc.2023.1183039
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author Bucher-Johannessen, Cecilie
Birkeland, Einar Elvbakken
Vinberg, Elina
Bemanian, Vahid
Hoff, Geir
Berstad, Paula
Rounge, Trine B.
author_facet Bucher-Johannessen, Cecilie
Birkeland, Einar Elvbakken
Vinberg, Elina
Bemanian, Vahid
Hoff, Geir
Berstad, Paula
Rounge, Trine B.
author_sort Bucher-Johannessen, Cecilie
collection PubMed
description BACKGROUND: The microbiome has been implicated in the initiation and progression of colorectal cancer (CRC) in cross-sectional studies. However, there is a lack of studies using prospectively collected samples. METHODS: From the Norwegian Colorectal Cancer Prevention (NORCCAP) trial, we analyzed 144 archived fecal samples from participants who were diagnosed with CRC or high-risk adenoma (HRA) at screening and from participants who remained cancer-free during 17 years of follow-up. We performed 16S rRNA sequencing of all the samples and metagenome sequencing on a subset of 47 samples. Differences in taxonomy and gene content between outcome groups were assessed for alpha and beta diversity and differential abundance. RESULTS: Diversity and composition analyses showed no significant differences between CRC, HRA, and healthy controls. Phascolarctobacterium succinatutens was more abundant in CRC compared with healthy controls in both the 16S and metagenome data. The abundance of Bifidobacterium and Lachnospiraceae spp. was associated with time to CRC diagnosis. CONCLUSION: Using a longitudinal study design, we identified three taxa as being potentially associated with CRC. These should be the focus of further studies of microbial changes occurring prior to CRC diagnosis.
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spelling pubmed-101726512023-05-12 Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing Bucher-Johannessen, Cecilie Birkeland, Einar Elvbakken Vinberg, Elina Bemanian, Vahid Hoff, Geir Berstad, Paula Rounge, Trine B. Front Oncol Oncology BACKGROUND: The microbiome has been implicated in the initiation and progression of colorectal cancer (CRC) in cross-sectional studies. However, there is a lack of studies using prospectively collected samples. METHODS: From the Norwegian Colorectal Cancer Prevention (NORCCAP) trial, we analyzed 144 archived fecal samples from participants who were diagnosed with CRC or high-risk adenoma (HRA) at screening and from participants who remained cancer-free during 17 years of follow-up. We performed 16S rRNA sequencing of all the samples and metagenome sequencing on a subset of 47 samples. Differences in taxonomy and gene content between outcome groups were assessed for alpha and beta diversity and differential abundance. RESULTS: Diversity and composition analyses showed no significant differences between CRC, HRA, and healthy controls. Phascolarctobacterium succinatutens was more abundant in CRC compared with healthy controls in both the 16S and metagenome data. The abundance of Bifidobacterium and Lachnospiraceae spp. was associated with time to CRC diagnosis. CONCLUSION: Using a longitudinal study design, we identified three taxa as being potentially associated with CRC. These should be the focus of further studies of microbial changes occurring prior to CRC diagnosis. Frontiers Media S.A. 2023-04-27 /pmc/articles/PMC10172651/ /pubmed/37182146 http://dx.doi.org/10.3389/fonc.2023.1183039 Text en Copyright © 2023 Bucher-Johannessen, Birkeland, Vinberg, Bemanian, Hoff, Berstad and Rounge 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
Bucher-Johannessen, Cecilie
Birkeland, Einar Elvbakken
Vinberg, Elina
Bemanian, Vahid
Hoff, Geir
Berstad, Paula
Rounge, Trine B.
Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title_full Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title_fullStr Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title_full_unstemmed Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title_short Long-term follow-up of colorectal cancer screening attendees identifies differences in Phascolarctobacterium spp. using 16S rRNA and metagenome sequencing
title_sort long-term follow-up of colorectal cancer screening attendees identifies differences in phascolarctobacterium spp. using 16s rrna and metagenome sequencing
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172651/
https://www.ncbi.nlm.nih.gov/pubmed/37182146
http://dx.doi.org/10.3389/fonc.2023.1183039
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