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Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection

BACKGROUND: Breast cancer belongs to the most frequent and severe cancer types in human. Since excretion of modified nucleosides from increased RNA metabolism has been proposed as a potential target in pathogenesis of breast cancer, the aim of the present study was to elucidate the predictability of...

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Autores principales: Henneges, Carsten, Bullinger, Dino, Fux, Richard, Friese, Natascha, Seeger, Harald, Neubauer, Hans, Laufer, Stefan, Gleiter, Christoph H, Schwab, Matthias, Zell, Andreas, Kammerer, Bernd
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680413/
https://www.ncbi.nlm.nih.gov/pubmed/19344524
http://dx.doi.org/10.1186/1471-2407-9-104
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author Henneges, Carsten
Bullinger, Dino
Fux, Richard
Friese, Natascha
Seeger, Harald
Neubauer, Hans
Laufer, Stefan
Gleiter, Christoph H
Schwab, Matthias
Zell, Andreas
Kammerer, Bernd
author_facet Henneges, Carsten
Bullinger, Dino
Fux, Richard
Friese, Natascha
Seeger, Harald
Neubauer, Hans
Laufer, Stefan
Gleiter, Christoph H
Schwab, Matthias
Zell, Andreas
Kammerer, Bernd
author_sort Henneges, Carsten
collection PubMed
description BACKGROUND: Breast cancer belongs to the most frequent and severe cancer types in human. Since excretion of modified nucleosides from increased RNA metabolism has been proposed as a potential target in pathogenesis of breast cancer, the aim of the present study was to elucidate the predictability of breast cancer by means of urinary excreted nucleosides. METHODS: We analyzed urine samples from 85 breast cancer women and respective healthy controls to assess the metabolic profiles of nucleosides by a comprehensive bioinformatic approach. All included nucleosides/ribosylated metabolites were isolated by cis-diol specific affinity chromatography and measured with liquid chromatography ion trap mass spectrometry (LC-ITMS). A valid set of urinary metabolites was selected by exclusion of all candidates with poor linearity and/or reproducibility in the analytical setting. The bioinformatic tool of Oscillating Search Algorithm for Feature Selection (OSAF) was applied to iteratively improve features for training of Support Vector Machines (SVM) to better predict breast cancer. RESULTS: After identification of 51 nucleosides/ribosylated metabolites in the urine of breast cancer women and/or controls by LC- ITMS coupling, a valid set of 35 candidates was selected for subsequent computational analyses. OSAF resulted in 44 pairwise ratios of metabolite features by iterative optimization. Based on this approach ultimately estimates for sensitivity and specificity of 83.5% and 90.6% were obtained for best prediction of breast cancer. The classification performance was dominated by metabolite pairs with SAH which highlights its importance for RNA methylation in cancer pathogenesis. CONCLUSION: Extensive RNA-pathway analysis based on mass spectrometric analysis of metabolites and subsequent bioinformatic feature selection allowed for the identification of significant metabolic features related to breast cancer pathogenesis. The combination of mass spectrometric analysis and subsequent SVM-based feature selection represents a promising tool for the development of a non-invasive prediction system.
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spelling pubmed-26804132009-05-12 Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection Henneges, Carsten Bullinger, Dino Fux, Richard Friese, Natascha Seeger, Harald Neubauer, Hans Laufer, Stefan Gleiter, Christoph H Schwab, Matthias Zell, Andreas Kammerer, Bernd BMC Cancer Research Article BACKGROUND: Breast cancer belongs to the most frequent and severe cancer types in human. Since excretion of modified nucleosides from increased RNA metabolism has been proposed as a potential target in pathogenesis of breast cancer, the aim of the present study was to elucidate the predictability of breast cancer by means of urinary excreted nucleosides. METHODS: We analyzed urine samples from 85 breast cancer women and respective healthy controls to assess the metabolic profiles of nucleosides by a comprehensive bioinformatic approach. All included nucleosides/ribosylated metabolites were isolated by cis-diol specific affinity chromatography and measured with liquid chromatography ion trap mass spectrometry (LC-ITMS). A valid set of urinary metabolites was selected by exclusion of all candidates with poor linearity and/or reproducibility in the analytical setting. The bioinformatic tool of Oscillating Search Algorithm for Feature Selection (OSAF) was applied to iteratively improve features for training of Support Vector Machines (SVM) to better predict breast cancer. RESULTS: After identification of 51 nucleosides/ribosylated metabolites in the urine of breast cancer women and/or controls by LC- ITMS coupling, a valid set of 35 candidates was selected for subsequent computational analyses. OSAF resulted in 44 pairwise ratios of metabolite features by iterative optimization. Based on this approach ultimately estimates for sensitivity and specificity of 83.5% and 90.6% were obtained for best prediction of breast cancer. The classification performance was dominated by metabolite pairs with SAH which highlights its importance for RNA methylation in cancer pathogenesis. CONCLUSION: Extensive RNA-pathway analysis based on mass spectrometric analysis of metabolites and subsequent bioinformatic feature selection allowed for the identification of significant metabolic features related to breast cancer pathogenesis. The combination of mass spectrometric analysis and subsequent SVM-based feature selection represents a promising tool for the development of a non-invasive prediction system. BioMed Central 2009-04-05 /pmc/articles/PMC2680413/ /pubmed/19344524 http://dx.doi.org/10.1186/1471-2407-9-104 Text en Copyright ©2009 Henneges et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Henneges, Carsten
Bullinger, Dino
Fux, Richard
Friese, Natascha
Seeger, Harald
Neubauer, Hans
Laufer, Stefan
Gleiter, Christoph H
Schwab, Matthias
Zell, Andreas
Kammerer, Bernd
Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title_full Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title_fullStr Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title_full_unstemmed Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title_short Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection
title_sort prediction of breast cancer by profiling of urinary rna metabolites using support vector machine-based feature selection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680413/
https://www.ncbi.nlm.nih.gov/pubmed/19344524
http://dx.doi.org/10.1186/1471-2407-9-104
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