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

BackgroundMetabolism 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.ResultsIn 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.ConclusionsBiomarker 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.

[1]  D. Fell Understanding the Control of Metabolism , 1996 .

[2]  Xiaobo Zhou,et al.  Predicting enzyme targets for cancer drugs by profiling human Metabolic reactions in NCI-60 cell lines , 2010, BMC Bioinformatics.

[3]  R. Codario Type 2 Diabetes, Pre-Diabetes, and the Metabolic Syndrome , 2005 .

[4]  Vassilios S. Vassiliadis,et al.  Metabolite biomarker discovery for metabolic diseases by flux analysis , 2012, 2012 IEEE 6th International Conference on Systems Biology (ISB).

[5]  Xiang-Sun Zhang,et al.  Two-stage flux balance analysis of metabolic networks for drug target identification , 2011, BMC Systems Biology.

[6]  G. Bell,et al.  Intrapancreatic delivery of human umbilical cord blood aldehyde dehydrogenase-producing cells promotes islet regeneration , 2012, Diabetologia.

[7]  Michael E. Lassman,et al.  Malonyl CoenzymeA Decarboxylase Regulates Lipid and Glucose Metabolism in Human Skeletal Muscle , 2008, Diabetes.

[8]  Anil K. Jain,et al.  Data clustering: a review , 1999, CSUR.

[9]  N. Saitou,et al.  The neighbor-joining method: a new method for reconstructing phylogenetic trees. , 1987, Molecular biology and evolution.

[10]  Chris H. Q. Ding,et al.  Link Analysis: Hubs and Authorities on the World Wide Web , 2004, SIAM Rev..

[11]  Yi Lu,et al.  Incremental genetic K-means algorithm and its application in gene expression data analysis , 2004, BMC Bioinformatics.

[12]  M. Andrades,et al.  Glycolaldehyde Induces Oxidative Stress in the Heart: A Clue to Diabetic Cardiomyopathy? , 2010, Cardiovascular Toxicology.

[13]  D. Ramkrishna,et al.  Metabolic Engineering from a Cybernetic Perspective. 1. Theoretical Preliminaries , 1999, Biotechnology progress.

[14]  S. Kaneko,et al.  Profile of rhythmic gene expression in the livers of obese diabetic KK-A(y) mice. , 2006, Biochemical and biophysical research communications.

[15]  J. Reich,et al.  Energy metabolism of the cell : a theoretical treatise , 1981 .

[16]  Yin Zhang,et al.  Solving large-scale linear programs by interior-point methods under the Matlab ∗ Environment † , 1998 .

[17]  Arnold M Saxton,et al.  Comparison of threshold selection methods for microarray gene co-expression matrices , 2009, BMC Research Notes.

[18]  D. Bonthron,et al.  Both isoforms of ketohexokinase are dispensable for normal growth and development. , 2010, Physiological genomics.

[19]  J. Bailey Complex biology with no parameters , 2001, Nature Biotechnology.

[20]  K. O'dea,et al.  The Longitudinal Effect of Inhibiting Fatty Acid Oxidation in Diabetic Rats Fed a High Fat Diet , 1992, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[21]  E. Ruppin,et al.  Predicting metabolic biomarkers of human inborn errors of metabolism , 2009, Molecular systems biology.

[22]  T. Hansen,et al.  Bioinformatics-Driven Identification and Examination of Candidate Genes for Non-Alcoholic Fatty Liver Disease , 2011, PloS one.

[23]  J. MacQueen Some methods for classification and analysis of multivariate observations , 1967 .

[24]  Patrik D'haeseleer,et al.  How does gene expression clustering work? , 2005, Nature Biotechnology.

[25]  Sanjay Ranka,et al.  An Iterative Algorithm for Metabolic Network-Based Drug Target Identification , 2006, Pacific Symposium on Biocomputing.

[26]  C. Newgard,et al.  Fatty Acid Oxidation and Insulin Action , 2008, Diabetes.

[27]  H. Ni,et al.  Etomoxir-induced oxidative stress in HepG2 cells detected by differential gene expression is confirmed biochemically. , 2002, Toxicological sciences : an official journal of the Society of Toxicology.

[28]  S. Kono,et al.  Genetic Polymorphisms of Alcohol Dehydrogenase and Aldehyde Dehydrogenase: Alcohol Use and Type 2 Diabetes in Japanese Men , 2011 .

[29]  Luonan Chen,et al.  Detecting drug targets with minimum side effects in metabolic networks. , 2009, IET systems biology.

[30]  Monica L. Mo,et al.  Global reconstruction of the human metabolic network based on genomic and bibliomic data , 2007, Proceedings of the National Academy of Sciences.

[31]  R. Codario Comprar Type 2 Diabetes, Pre-Diabetes, And The Metabolic Syndrome | Ronald A. Codario | 9781603274401 | Humana Press , 2011 .

[32]  Michael E. Lassman,et al.  MALONYL COENZYME A DECARBOXYLASE REGULATES LIPID AND GLUCOSE METABOLISM IN HUMAN SKELETAL MUSCLE , 2008 .

[33]  Kenneth J. Kauffman,et al.  Advances in flux balance analysis. , 2003, Current opinion in biotechnology.

[34]  David G. Stork,et al.  Pattern Classification , 1973 .

[35]  L. Rédei CHAPTER I – SET-THEORETICAL PRELIMINARIES , 1967 .

[36]  I. Goryanin,et al.  Human metabolic network reconstruction and its impact on drug discovery and development. , 2008, Drug discovery today.

[37]  N. Bhagavan,et al.  Carbohydrate Metabolism II: Gluconeogenesis, Glycogen Synthesis and Breakdown, and Alternative Pathways , 2002 .

[38]  Albert-László Barabási,et al.  The Activity Reaction Core and Plasticity of Metabolic Networks , 2005, PLoS Comput. Biol..

[39]  H. Öhlin,et al.  Aldehyde Dehydrogenase Activity and Large Vessel Disease in Diabetes Mellitus: A Preliminary Study , 1986, Diabetes.

[40]  Sergey Brin,et al.  The Anatomy of a Large-Scale Hypertextual Web Search Engine , 1998, Comput. Networks.

[41]  Michael A. Langston,et al.  Threshold selection in gene co-expression networks using spectral graph theory techniques , 2009, BMC Bioinformatics.

[42]  Benno Schwikowski,et al.  Graph-based methods for analysing networks in cell biology , 2006, Briefings Bioinform..

[43]  Bin Song,et al.  Mining Metabolic Networks for Optimal Drug Targets , 2007, Pacific Symposium on Biocomputing.

[44]  Yasuhiro Nakamura,et al.  The farnesoid X receptor regulates transcription of 3β-hydroxysteroid dehydrogenase type 2 in human adrenal cells , 2009, Molecular and Cellular Endocrinology.

[45]  R. Goodacre,et al.  Metabolic Profiling: Its Role in Biomarker Discovery and Gene Function Analysis , 2003, Springer US.

[46]  B. Palsson The challenges of in silico biology , 2000, Nature Biotechnology.