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Identification of microbial markers across populations in early detection of colorectal cancer
Associations between gut microbiota and colorectal cancer (CRC) have been widely investigated. However, the replicable markers for early-stage adenoma diagnosis across multiple populations remain elusive. Here, we perform an integrated analysis on 1056 public fecal samples, to identify adenoma-assoc...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144394/ https://www.ncbi.nlm.nih.gov/pubmed/34031391 http://dx.doi.org/10.1038/s41467-021-23265-y |
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author | Wu, Yuanqi Jiao, Na Zhu, Ruixin Zhang, Yida Wu, Dingfeng Wang, An-Jun Fang, Sa Tao, Liwen Li, Yichen Cheng, Sijing He, Xiaosheng Lan, Ping Tian, Chuan Liu, Ning-Ning Zhu, Lixin |
author_facet | Wu, Yuanqi Jiao, Na Zhu, Ruixin Zhang, Yida Wu, Dingfeng Wang, An-Jun Fang, Sa Tao, Liwen Li, Yichen Cheng, Sijing He, Xiaosheng Lan, Ping Tian, Chuan Liu, Ning-Ning Zhu, Lixin |
author_sort | Wu, Yuanqi |
collection | PubMed |
description | Associations between gut microbiota and colorectal cancer (CRC) have been widely investigated. However, the replicable markers for early-stage adenoma diagnosis across multiple populations remain elusive. Here, we perform an integrated analysis on 1056 public fecal samples, to identify adenoma-associated microbial markers for early detection of CRC. After adjusting for potential confounders, Random Forest classifiers are constructed with 11 markers to discriminate adenoma from control (area under the ROC curve (AUC) = 0.80), and 26 markers to discriminate adenoma from CRC (AUC = 0.89), respectively. Moreover, we validate the classifiers in two independent cohorts achieving AUCs of 0.78 and 0.84, respectively. Functional analysis reveals that the altered microbiome is characterized with increased ADP-l-glycero-beta-d-manno-heptose biosynthesis in adenoma and elevated menaquinone-10 biosynthesis in CRC. These findings are validated in a newly-collected cohort of 43 samples using quantitative real-time PCR. This work proves the validity of adenoma-specific markers across multi-populations, which would contribute to the early diagnosis and treatment of CRC. |
format | Online Article Text |
id | pubmed-8144394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81443942021-06-07 Identification of microbial markers across populations in early detection of colorectal cancer Wu, Yuanqi Jiao, Na Zhu, Ruixin Zhang, Yida Wu, Dingfeng Wang, An-Jun Fang, Sa Tao, Liwen Li, Yichen Cheng, Sijing He, Xiaosheng Lan, Ping Tian, Chuan Liu, Ning-Ning Zhu, Lixin Nat Commun Article Associations between gut microbiota and colorectal cancer (CRC) have been widely investigated. However, the replicable markers for early-stage adenoma diagnosis across multiple populations remain elusive. Here, we perform an integrated analysis on 1056 public fecal samples, to identify adenoma-associated microbial markers for early detection of CRC. After adjusting for potential confounders, Random Forest classifiers are constructed with 11 markers to discriminate adenoma from control (area under the ROC curve (AUC) = 0.80), and 26 markers to discriminate adenoma from CRC (AUC = 0.89), respectively. Moreover, we validate the classifiers in two independent cohorts achieving AUCs of 0.78 and 0.84, respectively. Functional analysis reveals that the altered microbiome is characterized with increased ADP-l-glycero-beta-d-manno-heptose biosynthesis in adenoma and elevated menaquinone-10 biosynthesis in CRC. These findings are validated in a newly-collected cohort of 43 samples using quantitative real-time PCR. This work proves the validity of adenoma-specific markers across multi-populations, which would contribute to the early diagnosis and treatment of CRC. Nature Publishing Group UK 2021-05-24 /pmc/articles/PMC8144394/ /pubmed/34031391 http://dx.doi.org/10.1038/s41467-021-23265-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Yuanqi Jiao, Na Zhu, Ruixin Zhang, Yida Wu, Dingfeng Wang, An-Jun Fang, Sa Tao, Liwen Li, Yichen Cheng, Sijing He, Xiaosheng Lan, Ping Tian, Chuan Liu, Ning-Ning Zhu, Lixin Identification of microbial markers across populations in early detection of colorectal cancer |
title | Identification of microbial markers across populations in early detection of colorectal cancer |
title_full | Identification of microbial markers across populations in early detection of colorectal cancer |
title_fullStr | Identification of microbial markers across populations in early detection of colorectal cancer |
title_full_unstemmed | Identification of microbial markers across populations in early detection of colorectal cancer |
title_short | Identification of microbial markers across populations in early detection of colorectal cancer |
title_sort | identification of microbial markers across populations in early detection of colorectal cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144394/ https://www.ncbi.nlm.nih.gov/pubmed/34031391 http://dx.doi.org/10.1038/s41467-021-23265-y |
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