• DocumentCode
    1345568
  • Title

    Cross-platform method for identifying candidate network biomarkers for prostate cancer

  • Author

    Jin, Guang ; Zhou, Xiaoxin ; Cui, K. ; Zhang, X.S. ; Chen, Luo-nan ; Wong, Stephen T. C.

  • Author_Institution
    Weill Cornell Med. Coll., Med. Syst. Biol. Lab., Cornell Univ., Houston, TX, USA
  • Volume
    3
  • Issue
    6
  • fYear
    2009
  • Firstpage
    505
  • Lastpage
    512
  • Abstract
    Discovering biomarkers using mass spectrometry (MS) and microarray expression profiles is a promising strategy in molecular diagnosis. Here, the authors proposed a new pipeline for biomarker discovery that integrates disease information for proteins and genes, expression profiles in both genomic and proteomic levels, and protein-protein interactions (PPIs) to discover high confidence network biomarkers. Using this pipeline, a total of 474 molecules (genes and proteins) related to prostate cancer were identified and a prostate-cancer-related network (PCRN) was derived from the integrative information. Thus, a set of candidate network biomarkers were identified from multiple expression profiles composed by eight microarray datasets and one proteomics dataset. The network biomarkers with PPIs can accurately distinguish the prostate patients from the normal ones, which potentially provide more reliable hits of biomarker candidates than conventional biomarker discovery methods.
  • Keywords
    biological organs; cancer; genetics; genomics; mass spectroscopic chemical analysis; medical computing; proteins; proteomics; tumours; biomarkers; cross-platform method; disease information; gene expression; genomic level; mass spectrometry; microarray datasets; microarray expression profile; molecular diagnosis; prostate cancer; protein-protein interactions; proteomics;
  • fLanguage
    English
  • Journal_Title
    Systems Biology, IET
  • Publisher
    iet
  • ISSN
    1751-8849
  • Type

    jour

  • DOI
    10.1049/iet-syb.2008.0168
  • Filename
    5344680