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Staging of colorectal cancer using lipid biomarkers and machine learning

INTRODUCTION: Colorectal cancer (CRC) is the third most commonly diagnosed cancer worldwide. Alteration in lipid metabolism and chemokine expression are considered hallmark characteristics of malignant progression and metastasis of CRC. Validated diagnostic and prognostic biomarkers are urgently nee...

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Autores principales: Krishnan, Sanduru Thamarai, Winkler, David, Creek, Darren, Anderson, Dovile, Kirana, Chandra, Maddern, Guy J, Fenix, Kevin, Hauben, Ehud, Rudd, David, Voelcker, Nicolas Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511619/
https://www.ncbi.nlm.nih.gov/pubmed/37731020
http://dx.doi.org/10.1007/s11306-023-02049-z
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author Krishnan, Sanduru Thamarai
Winkler, David
Creek, Darren
Anderson, Dovile
Kirana, Chandra
Maddern, Guy J
Fenix, Kevin
Hauben, Ehud
Rudd, David
Voelcker, Nicolas Hans
author_facet Krishnan, Sanduru Thamarai
Winkler, David
Creek, Darren
Anderson, Dovile
Kirana, Chandra
Maddern, Guy J
Fenix, Kevin
Hauben, Ehud
Rudd, David
Voelcker, Nicolas Hans
author_sort Krishnan, Sanduru Thamarai
collection PubMed
description INTRODUCTION: Colorectal cancer (CRC) is the third most commonly diagnosed cancer worldwide. Alteration in lipid metabolism and chemokine expression are considered hallmark characteristics of malignant progression and metastasis of CRC. Validated diagnostic and prognostic biomarkers are urgently needed to define molecular heterogeneous CRC clinical stages and subtypes, as liver dominant metastasis has poor survival outcomes. OBJECTIVES: The aim of this study was to integrate lipid changes, concentrations of chemokines, such as platelet factor 4 and interleukin 8, and gene marker status measured in plasma samples, with clinical features from patients at different CRC stages or who had progressed to stage-IV colorectal liver metastasis (CLM). METHODS: High-resolution liquid chromatography-mass spectrometry (HR-LC-MS) was used to determine the levels of candidate lipid biomarkers in each CRC patient’s preoperative plasma samples and combined with chemokine, gene and clinical data. Machine learning models were then trained using known clinical outcomes to select biomarker combinations that best classify CRC stage and group. RESULTS: Bayesian neural net and multilinear regression-machine learning identified candidate biomarkers that classify CRC (stages I-III), CLM patients and control subjects (cancer-free or patients with polyps/diverticulitis), showing that integrating specific lipid signatures and chemokines (platelet factor-4 and interluken-8; IL-8) can improve prognostic accuracy. Gene marker status could contribute to disease prediction, but requires ubiquitous testing in clinical cohorts. CONCLUSION: Our findings demonstrate that correlating multiple disease related features with lipid changes could improve CRC prognosis. The identified signatures could be used as reference biomarkers to predict CRC prognosis and classify stages, and monitor therapeutic intervention. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-02049-z.
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spelling pubmed-105116192023-09-22 Staging of colorectal cancer using lipid biomarkers and machine learning Krishnan, Sanduru Thamarai Winkler, David Creek, Darren Anderson, Dovile Kirana, Chandra Maddern, Guy J Fenix, Kevin Hauben, Ehud Rudd, David Voelcker, Nicolas Hans Metabolomics Original Article INTRODUCTION: Colorectal cancer (CRC) is the third most commonly diagnosed cancer worldwide. Alteration in lipid metabolism and chemokine expression are considered hallmark characteristics of malignant progression and metastasis of CRC. Validated diagnostic and prognostic biomarkers are urgently needed to define molecular heterogeneous CRC clinical stages and subtypes, as liver dominant metastasis has poor survival outcomes. OBJECTIVES: The aim of this study was to integrate lipid changes, concentrations of chemokines, such as platelet factor 4 and interleukin 8, and gene marker status measured in plasma samples, with clinical features from patients at different CRC stages or who had progressed to stage-IV colorectal liver metastasis (CLM). METHODS: High-resolution liquid chromatography-mass spectrometry (HR-LC-MS) was used to determine the levels of candidate lipid biomarkers in each CRC patient’s preoperative plasma samples and combined with chemokine, gene and clinical data. Machine learning models were then trained using known clinical outcomes to select biomarker combinations that best classify CRC stage and group. RESULTS: Bayesian neural net and multilinear regression-machine learning identified candidate biomarkers that classify CRC (stages I-III), CLM patients and control subjects (cancer-free or patients with polyps/diverticulitis), showing that integrating specific lipid signatures and chemokines (platelet factor-4 and interluken-8; IL-8) can improve prognostic accuracy. Gene marker status could contribute to disease prediction, but requires ubiquitous testing in clinical cohorts. CONCLUSION: Our findings demonstrate that correlating multiple disease related features with lipid changes could improve CRC prognosis. The identified signatures could be used as reference biomarkers to predict CRC prognosis and classify stages, and monitor therapeutic intervention. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11306-023-02049-z. Springer US 2023-09-20 2023 /pmc/articles/PMC10511619/ /pubmed/37731020 http://dx.doi.org/10.1007/s11306-023-02049-z 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/) .
spellingShingle Original Article
Krishnan, Sanduru Thamarai
Winkler, David
Creek, Darren
Anderson, Dovile
Kirana, Chandra
Maddern, Guy J
Fenix, Kevin
Hauben, Ehud
Rudd, David
Voelcker, Nicolas Hans
Staging of colorectal cancer using lipid biomarkers and machine learning
title Staging of colorectal cancer using lipid biomarkers and machine learning
title_full Staging of colorectal cancer using lipid biomarkers and machine learning
title_fullStr Staging of colorectal cancer using lipid biomarkers and machine learning
title_full_unstemmed Staging of colorectal cancer using lipid biomarkers and machine learning
title_short Staging of colorectal cancer using lipid biomarkers and machine learning
title_sort staging of colorectal cancer using lipid biomarkers and machine learning
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511619/
https://www.ncbi.nlm.nih.gov/pubmed/37731020
http://dx.doi.org/10.1007/s11306-023-02049-z
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