• DocumentCode
    573700
  • Title

    Using NMFAS to identify key biological pathways associated with human diseases

  • Author

    Hao Guo ; Yunping Zhu ; Dong Li ; Fuchu He ; Qijun Liu

  • Author_Institution
    State Key Lab. of Proteomics, Beijing Inst. of Radiat. Med., Beijing, China
  • fYear
    2012
  • fDate
    18-20 Aug. 2012
  • Firstpage
    79
  • Lastpage
    85
  • Abstract
    Gene expression microarray enables us to measure the gene expression levels for thousands of genes at the same time. Here, we constructed the non-negative matrix factorization analysis strategy (NMFAS) to dig the underlying biological pathways related with various diseases by factorizing the pathway expression matrix, which was extracted from microarray matrix using pathway membership information, into the product of row and column vectors. We defined row vector as the pathway activity and column vector as the gene contribution weight. Via comparing the pathway activity of two different sample groups, we can identify significantly expressed pathways. We applied this strategy on two different cases: smoking and type 2 diabetes (DM2). We found 152 differentially expressed pathways by the comparison of pathway activity between smoker and never smoker, including pathways that have been validated in literature, such as “O-Glycans biosynthesis” and “Glutathione metabolism”. We also found important genes related to smoking phenotype, such as NQO, HSPA1A, ALDH3A1. As for DM2 analysis, our results suggested 9 pathways were significantly expressed, including typical pathways like “Oxidative phosphorylation” and “mTOR signaling pathway”, and found genes like CAPNS1, APP, COX7A1, COX7B, which might play important roles in the cellular regulations of DM2. In conclusion, Our strategy can be efficiently used to integrate gene expression profiles and biological pathway information to identify the key processes underlying human disease and can identify gene pathways missed by alternative approaches.
  • Keywords
    bioinformatics; diseases; genetics; knowledge engineering; lab-on-a-chip; matrix decomposition; ALDH3A1; APP; CAPNS1; COX7A1; COX7B; HSPA1A; NMFAS; NQO; disease associated biological pathways; gene contribution weight; gene expression levels; gene expression microarray; glutathione metabolism; mTOR signaling pathway; microarray matrix; nonnegative matrix factorization analysis strategy; o-glycans biosynthesis; oxidative phosphorylation; pathway activity; pathway expression matrix factorization; pathway membership information; smoking data; smoking phenotype; type 2 diabetes data; Biochemistry; Cancer; Diabetes; Diseases; Gene expression; Vectors; microarray; non-negative matrix factorization; pathways; smoking; type 2 diabetes;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Systems Biology (ISB), 2012 IEEE 6th International Conference on
  • Conference_Location
    Xi´an
  • Print_ISBN
    978-1-4673-4396-1
  • Electronic_ISBN
    978-1-4673-4397-8
  • Type

    conf

  • DOI
    10.1109/ISB.2012.6314116
  • Filename
    6314116