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      Multi-omics machine learning to study host-microbiome interactions in early-onset colorectal cancer

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          Abstract

          The incidence of early-onset colorectal cancer (eoCRC) is rising, and its pathogenesis is not completely understood. We hypothesized that machine learning utilizing paired tissue microbiome and plasma metabolome features could uncover distinct host-microbiome associations between eoCRC and average-onset CRC (aoCRC). Individuals with stages I–IV CRC ( n = 64) were categorized as eoCRC (age ≤ 50, n = 20) or aoCRC (age ≥ 60, n = 44). Untargeted plasma metabolomics and 16S rRNA amplicon sequencing (microbiome analysis) of tumor tissue were performed. We fit DIABLO (Data Integration Analysis for Biomarker Discovery using Latent variable approaches for Omics studies) to construct a supervised machine-learning classifier using paired multi-omics (microbiome and metabolomics) data and identify associations unique to eoCRC. A differential association network analysis was also performed. Distinct clustering patterns emerged in multi-omic dimension reduction analysis. The metabolomics classifier achieved an AUC of 0.98, compared to AUC 0.61 for microbiome-based classifier. Circular correlation technique highlighted several key associations. Metabolites glycerol and pseudouridine (higher abundance in individuals with aoCRC) had negative correlations with Parasutterella, and Ruminococcaceae (higher abundance in individuals with eoCRC). Cholesterol and xylitol correlated negatively with Erysipelatoclostridium and Eubacterium, and showed a positive correlation with Acidovorax with higher abundance in individuals with eoCRC. Network analysis revealed different clustering patterns and associations for several metabolites e.g.: urea cycle metabolites and microbes such as Akkermansia. We show that multi-omics analysis can be utilized to study host-microbiome correlations in eoCRC and demonstrates promising biomarker potential of a metabolomics classifier. The distinct host-microbiome correlations for urea cycle in eoCRC may offer opportunities for therapeutic interventions.

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          Most cited references53

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            DADA2: High resolution sample inference from Illumina amplicon data

            We present DADA2, a software package that models and corrects Illumina-sequenced amplicon errors. DADA2 infers sample sequences exactly, without coarse-graining into OTUs, and resolves differences of as little as one nucleotide. In several mock communities DADA2 identified more real variants and output fewer spurious sequences than other methods. We applied DADA2 to vaginal samples from a cohort of pregnant women, revealing a diversity of previously undetected Lactobacillus crispatus variants.
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              Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2

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                Author and article information

                Contributors
                kamaths@ccf.org
                Journal
                NPJ Precis Oncol
                NPJ Precis Oncol
                NPJ Precision Oncology
                Nature Publishing Group UK (London )
                2397-768X
                17 July 2024
                17 July 2024
                2024
                : 8
                : 146
                Affiliations
                [1 ]Department of Hematology-Oncology, Taussig Cancer Institute, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [2 ]Department of Medical Oncology, Dana-Farber Cancer Institute, ( https://ror.org/02jzgtq86) Boston, MA USA
                [3 ]Microbial Sequencing & Analytics Resource (MSAAR), Lerner Research Institute, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [4 ]Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [5 ]Center for Quantitative Metabolic Research, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [6 ]Department of Surgery, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [7 ]Case Comprehensive Cancer Center, ( https://ror.org/00fpjq451) Cleveland, OH USA
                [8 ]Department of Hematology-Oncology, University Hospital Seidman Cancer Center, ( https://ror.org/02kb97560) Cleveland, OH USA
                [9 ]Center for Young-Onset Colorectal Cancer, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [10 ]Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                [11 ]Population and Cancer Prevention Program, Case Comprehensive Cancer Center, ( https://ror.org/00fpjq451) Cleveland, OH USA
                [12 ]Department of Colorectal Surgery, Digestive Disease & Surgery Institute, Cleveland Clinic, ( https://ror.org/03xjacd83) Cleveland, OH USA
                Author information
                http://orcid.org/0000-0002-3636-0353
                http://orcid.org/0000-0002-5313-9992
                http://orcid.org/0000-0003-0432-2536
                Article
                647
                10.1038/s41698-024-00647-1
                11255257
                39020083
                c8207a8f-18d4-4713-b28f-9a2c35b521a9
                © The Author(s) 2024

                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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 February 2024
                : 9 July 2024
                Funding
                Funded by: The Sondra and Stephen Hardis Chair in Oncology Research
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2024

                biomarkers,translational research,colorectal cancer,metabolomics,sequencing

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