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Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes

Cancer can be generally defined as a cluster of systematic diseases triggered by abnormal cell proliferation and growth. With the development of biological sciences and biotechnologies, the etiology of cancer is partially revealed, including some of the most substantial pathogenic factors [either en...

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Autores principales: Chen, Lei, Li, Zhandong, Zeng, Tao, Zhang, Yu-Hang, Liu, Dejing, Li, Hao, Huang, Tao, Cai, Yu-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672214/
https://www.ncbi.nlm.nih.gov/pubmed/33330634
http://dx.doi.org/10.3389/fmolb.2020.604794
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author Chen, Lei
Li, Zhandong
Zeng, Tao
Zhang, Yu-Hang
Liu, Dejing
Li, Hao
Huang, Tao
Cai, Yu-Dong
author_facet Chen, Lei
Li, Zhandong
Zeng, Tao
Zhang, Yu-Hang
Liu, Dejing
Li, Hao
Huang, Tao
Cai, Yu-Dong
author_sort Chen, Lei
collection PubMed
description Cancer can be generally defined as a cluster of systematic diseases triggered by abnormal cell proliferation and growth. With the development of biological sciences and biotechnologies, the etiology of cancer is partially revealed, including some of the most substantial pathogenic factors [either endogenous (genetics) or exogenous (environmental)]. However, some remaining factors that contribute to the tumorigenesis but have not been analyzed and discussed in detail remain. For instance, some typical correlations between microorganisms and tumorigenesis have been reported already, but previous studies are just sporadic studies on single microorganism–cancer subtype pairs and do not explain and validate the specific contribution of microbiome on tumorigenesis. On the basis of the systematic microbiome analyses of blood and cancer-associated tissues in cancer patients/controls in public domain, we performed interpretable analyses. We identified several core regulatory microorganisms that contribute to the classification of multiple tumor subtypes and established quantitative predictive models for interpretable prediction by using multiple machine learning methods. We also compared the optimal features (microorganisms) and rules identified from microbiome profiles processed using the Kraken and the SHOGUN. Collectively, our study identified new microbiome signatures and their interpretable classification rules for cancer discrimination and carried out reliable methodological comparison for robust cancer microbiome analyses, thereby promoting the development of tumor etiology at the microbiome level.
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spelling pubmed-76722142020-12-15 Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes Chen, Lei Li, Zhandong Zeng, Tao Zhang, Yu-Hang Liu, Dejing Li, Hao Huang, Tao Cai, Yu-Dong Front Mol Biosci Molecular Biosciences Cancer can be generally defined as a cluster of systematic diseases triggered by abnormal cell proliferation and growth. With the development of biological sciences and biotechnologies, the etiology of cancer is partially revealed, including some of the most substantial pathogenic factors [either endogenous (genetics) or exogenous (environmental)]. However, some remaining factors that contribute to the tumorigenesis but have not been analyzed and discussed in detail remain. For instance, some typical correlations between microorganisms and tumorigenesis have been reported already, but previous studies are just sporadic studies on single microorganism–cancer subtype pairs and do not explain and validate the specific contribution of microbiome on tumorigenesis. On the basis of the systematic microbiome analyses of blood and cancer-associated tissues in cancer patients/controls in public domain, we performed interpretable analyses. We identified several core regulatory microorganisms that contribute to the classification of multiple tumor subtypes and established quantitative predictive models for interpretable prediction by using multiple machine learning methods. We also compared the optimal features (microorganisms) and rules identified from microbiome profiles processed using the Kraken and the SHOGUN. Collectively, our study identified new microbiome signatures and their interpretable classification rules for cancer discrimination and carried out reliable methodological comparison for robust cancer microbiome analyses, thereby promoting the development of tumor etiology at the microbiome level. Frontiers Media S.A. 2020-11-04 /pmc/articles/PMC7672214/ /pubmed/33330634 http://dx.doi.org/10.3389/fmolb.2020.604794 Text en Copyright © 2020 Chen, Li, Zeng, Zhang, Liu, Li, Huang and Cai. 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 Molecular Biosciences
Chen, Lei
Li, Zhandong
Zeng, Tao
Zhang, Yu-Hang
Liu, Dejing
Li, Hao
Huang, Tao
Cai, Yu-Dong
Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title_full Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title_fullStr Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title_full_unstemmed Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title_short Identifying Robust Microbiota Signatures and Interpretable Rules to Distinguish Cancer Subtypes
title_sort identifying robust microbiota signatures and interpretable rules to distinguish cancer subtypes
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672214/
https://www.ncbi.nlm.nih.gov/pubmed/33330634
http://dx.doi.org/10.3389/fmolb.2020.604794
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