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Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models
BACKGROUND: Colorectal cancer (CRC) is a heterogeneous disease, with subtypes that have different clinical behaviours and subsequent prognoses. There is a growing body of evidence suggesting that right-sided colorectal cancer (RCC) and left-sided colorectal cancer (LCC) also differ in treatment succ...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337110/ https://www.ncbi.nlm.nih.gov/pubmed/37434131 http://dx.doi.org/10.1186/s12885-023-10848-9 |
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author | Kolisnik, Tyler Sulit, Arielle Kae Schmeier, Sebastian Frizelle, Frank Purcell, Rachel Smith, Adam Silander, Olin |
author_facet | Kolisnik, Tyler Sulit, Arielle Kae Schmeier, Sebastian Frizelle, Frank Purcell, Rachel Smith, Adam Silander, Olin |
author_sort | Kolisnik, Tyler |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is a heterogeneous disease, with subtypes that have different clinical behaviours and subsequent prognoses. There is a growing body of evidence suggesting that right-sided colorectal cancer (RCC) and left-sided colorectal cancer (LCC) also differ in treatment success and patient outcomes. Biomarkers that differentiate between RCC and LCC are not well-established. Here, we apply random forest (RF) machine learning methods to identify genomic or microbial biomarkers that differentiate RCC and LCC. METHODS: RNA-seq expression data for 58,677 coding and non-coding human genes and count data for 28,557 human unmapped reads were obtained from 308 patient CRC tumour samples. We created three RF models for datasets of human genes-only, microbes-only, and genes-and-microbes combined. We used a permutation test to identify features of significant importance. Finally, we used differential expression (DE) and paired Wilcoxon-rank sum tests to associate features with a particular side. RESULTS: RF model accuracy scores were 90%, 70%, and 87% with area under curve (AUC) of 0.9, 0.76, and 0.89 for the human genomic, microbial, and combined feature sets, respectively. 15 features were identified as significant in the model of genes-only, 54 microbes in the model of microbes-only, and 28 genes and 18 microbes in the model with genes-and-microbes combined. PRAC1 expression was the most important feature for differentiating RCC and LCC in the genes-only model, with HOXB13, SPAG16, HOXC4, and RNLS also playing a role. Ruminococcus gnavus and Clostridium acetireducens were the most important in the microbial-only model. MYOM3, HOXC4, Coprococcus eutactus, PRAC1, lncRNA AC012531.25, Ruminococcus gnavus, RNLS, HOXC6, SPAG16 and Fusobacterium nucleatum were most important in the combined model. CONCLUSIONS: Many of the identified genes and microbes among all models have previously established associations with CRC. However, the ability of RF models to account for inter-feature relationships within the underlying decision trees may yield a more sensitive and biologically interconnected set of genomic and microbial biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10848-9. |
format | Online Article Text |
id | pubmed-10337110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103371102023-07-13 Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models Kolisnik, Tyler Sulit, Arielle Kae Schmeier, Sebastian Frizelle, Frank Purcell, Rachel Smith, Adam Silander, Olin BMC Cancer Research BACKGROUND: Colorectal cancer (CRC) is a heterogeneous disease, with subtypes that have different clinical behaviours and subsequent prognoses. There is a growing body of evidence suggesting that right-sided colorectal cancer (RCC) and left-sided colorectal cancer (LCC) also differ in treatment success and patient outcomes. Biomarkers that differentiate between RCC and LCC are not well-established. Here, we apply random forest (RF) machine learning methods to identify genomic or microbial biomarkers that differentiate RCC and LCC. METHODS: RNA-seq expression data for 58,677 coding and non-coding human genes and count data for 28,557 human unmapped reads were obtained from 308 patient CRC tumour samples. We created three RF models for datasets of human genes-only, microbes-only, and genes-and-microbes combined. We used a permutation test to identify features of significant importance. Finally, we used differential expression (DE) and paired Wilcoxon-rank sum tests to associate features with a particular side. RESULTS: RF model accuracy scores were 90%, 70%, and 87% with area under curve (AUC) of 0.9, 0.76, and 0.89 for the human genomic, microbial, and combined feature sets, respectively. 15 features were identified as significant in the model of genes-only, 54 microbes in the model of microbes-only, and 28 genes and 18 microbes in the model with genes-and-microbes combined. PRAC1 expression was the most important feature for differentiating RCC and LCC in the genes-only model, with HOXB13, SPAG16, HOXC4, and RNLS also playing a role. Ruminococcus gnavus and Clostridium acetireducens were the most important in the microbial-only model. MYOM3, HOXC4, Coprococcus eutactus, PRAC1, lncRNA AC012531.25, Ruminococcus gnavus, RNLS, HOXC6, SPAG16 and Fusobacterium nucleatum were most important in the combined model. CONCLUSIONS: Many of the identified genes and microbes among all models have previously established associations with CRC. However, the ability of RF models to account for inter-feature relationships within the underlying decision trees may yield a more sensitive and biologically interconnected set of genomic and microbial biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10848-9. BioMed Central 2023-07-11 /pmc/articles/PMC10337110/ /pubmed/37434131 http://dx.doi.org/10.1186/s12885-023-10848-9 Text en © The Author(s) 2023 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 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kolisnik, Tyler Sulit, Arielle Kae Schmeier, Sebastian Frizelle, Frank Purcell, Rachel Smith, Adam Silander, Olin Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title | Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title_full | Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title_fullStr | Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title_full_unstemmed | Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title_short | Identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
title_sort | identifying important microbial and genomic biomarkers for differentiating right- versus left-sided colorectal cancer using random forest models |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10337110/ https://www.ncbi.nlm.nih.gov/pubmed/37434131 http://dx.doi.org/10.1186/s12885-023-10848-9 |
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