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Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach

BACKGROUND: Metabolism is a vital cellular process, and its malfunction can be a major contributor to many human diseases. Metabolites can serve as a metabolic disease biomarker. An detection of such biomarkers plays a significant role in the study of biochemical reaction and signaling networks. Ear...

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Autores principales: Li, Limin, Jiang, Hao, Qiu, Yushan, Ching, Wai-Ki, Vassiliadis, Vassilios S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866256/
https://www.ncbi.nlm.nih.gov/pubmed/24564929
http://dx.doi.org/10.1186/1752-0509-7-S2-S13
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author Li, Limin
Jiang, Hao
Qiu, Yushan
Ching, Wai-Ki
Vassiliadis, Vassilios S
author_facet Li, Limin
Jiang, Hao
Qiu, Yushan
Ching, Wai-Ki
Vassiliadis, Vassilios S
author_sort Li, Limin
collection PubMed
description BACKGROUND: Metabolism is a vital cellular process, and its malfunction can be a major contributor to many human diseases. Metabolites can serve as a metabolic disease biomarker. An detection of such biomarkers plays a significant role in the study of biochemical reaction and signaling networks. Early research mainly focused on the analysis of the metabolic networks. The issue of integrating metabolite networks with other available biological data to reveal the mechanics of disease-metabolite associations is an important and interesting challenge. RESULTS: In this article, we propose two new approaches for the identification of metabolic biomarkers with the incorporation of disease specific gene expression data and the genome-scale human metabolic network. The first approach is to compare the flux interval between the normal and disease sample so as to identify reaction biomarkers. The second one is based on the Reaction-Reaction Network (RRN) to reveal the significant reactions. These two approaches utilize reaction flux obtained by a Linear Programming (LP) based method that can contribute to the discovery of potential novel biomarkers. CONCLUSIONS: Biomarker identification is an important issue in studying biochemical reactions and signaling networks. Two efficient and effective computational methods are proposed for the identification of biomarkers in this article. Furthermore, the biomarkers found by our proposed methods are shown to be significant determinants for diabetes.
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spelling pubmed-38662562013-12-20 Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach Li, Limin Jiang, Hao Qiu, Yushan Ching, Wai-Ki Vassiliadis, Vassilios S BMC Syst Biol Research BACKGROUND: Metabolism is a vital cellular process, and its malfunction can be a major contributor to many human diseases. Metabolites can serve as a metabolic disease biomarker. An detection of such biomarkers plays a significant role in the study of biochemical reaction and signaling networks. Early research mainly focused on the analysis of the metabolic networks. The issue of integrating metabolite networks with other available biological data to reveal the mechanics of disease-metabolite associations is an important and interesting challenge. RESULTS: In this article, we propose two new approaches for the identification of metabolic biomarkers with the incorporation of disease specific gene expression data and the genome-scale human metabolic network. The first approach is to compare the flux interval between the normal and disease sample so as to identify reaction biomarkers. The second one is based on the Reaction-Reaction Network (RRN) to reveal the significant reactions. These two approaches utilize reaction flux obtained by a Linear Programming (LP) based method that can contribute to the discovery of potential novel biomarkers. CONCLUSIONS: Biomarker identification is an important issue in studying biochemical reactions and signaling networks. Two efficient and effective computational methods are proposed for the identification of biomarkers in this article. Furthermore, the biomarkers found by our proposed methods are shown to be significant determinants for diabetes. BioMed Central 2013-12-17 /pmc/articles/PMC3866256/ /pubmed/24564929 http://dx.doi.org/10.1186/1752-0509-7-S2-S13 Text en Copyright © 2013 Li 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Limin
Jiang, Hao
Qiu, Yushan
Ching, Wai-Ki
Vassiliadis, Vassilios S
Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title_full Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title_fullStr Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title_full_unstemmed Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title_short Discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
title_sort discovery of metabolite biomarkers: flux analysis and reaction-reaction network approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866256/
https://www.ncbi.nlm.nih.gov/pubmed/24564929
http://dx.doi.org/10.1186/1752-0509-7-S2-S13
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