Identification of colorectal cancer related genes with mRMR and shortest path in protein-protein interaction network

• Published in: PloS one 2012-04, Vol.7 (4), p.e33393-e33393
• Main Authors: Li, Bi-Qing, Huang, Tao, Liu, Lei, Cai, Yu-Dong, Chou, Kuo-Chen
• Format: Article
• Language: English
• Subjects: Algorithms; Apoptosis; Biology; Biomarkers, Tumor - genetics; Biomarkers, Tumor - metabolism; Cancer; Cancer genetics; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - genetics; Colorectal Neoplasms - metabolism; Computational Biology; Computer applications; Computer Simulation; Enzymes; Gastrointestinal diseases; Gene expression; Gene Expression Profiling; Gene Regulatory Networks; Genes; Genetic aspects; Humans; Kinases; Laboratories; Life sciences; Localization; Medicine; Mutation; Oligonucleotide Array Sequence Analysis; Prostate cancer; Protein interaction; Protein Interaction Maps; Protein-protein interactions; Proteins; Redundancy; Shortest-path problems; Signal Transduction; Software; Tissues; Transcription factors; Tumors
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0033393

One of the most important and challenging problems in biomedicine and genomics is how to identify the disease genes. In this study, we developed a computational method to identify colorectal cancer-related genes based on (i) the gene expression profiles, and (ii) the shortest path analysis of functional protein association networks. The former has been used to select differentially expressed genes as disease genes for quite a long time, while the latter has been widely used to study the mechanism of diseases. With the existing protein-protein interaction data from STRING (Search Tool for the Retrieval of Interacting Genes), a weighted functional protein association network was constructed. By means of the mRMR (Maximum Relevance Minimum Redundancy) approach, six genes were identified that can distinguish the colorectal tumors and normal adjacent colonic tissues from their gene expression profiles. Meanwhile, according to the shortest path approach, we further found an additional 35 genes, of which some have been reported to be relevant to colorectal cancer and some are very likely to be relevant to it. Interestingly, the genes we identified from both the gene expression profiles and the functional protein association network have more cancer genes than the genes identified from the gene expression profiles alone. Besides, these genes also had greater functional similarity with the reported colorectal cancer genes than the genes identified from the gene expression profiles alone. All these indicate that our method as presented in this paper is quite promising. The method may become a useful tool, or at least plays a complementary role to the existing method, for identifying colorectal cancer genes. It has not escaped our notice that the method can be applied to identify the genes of other diseases as well.