Motivation and Aim: Glioblastoma is the most aggressive type of brain tumors resistant to a number of antitumor drugs. The problem of therapy and drug treatment course is complicated by extremely high heterogeneity in the benign cell populations, the random arrangement of tumor cells, and polymorphism of their nuclei. The pathogenesis of gliomas needs to be studied using modern technologies to find new therapy targets. For an object such as gliomas, it is necessary to conduct new studies based on modern cellular technologies, genome-wide technologies for high-throughput sequencing, and the integration of available information from international databases and genomic projects [2].
Methods and Algorithms:There are open international databases on gene expression including glioblastoma (microarrays and sequencing data of GEO NCBI, http://www.ncbi.nlm.nih.gov/geoprofiles/), expression in various types of tumor cells (The Cancer Gene Atlas, cancergenome.nih.gov), gene expression for brain compartments (Allen Brain Atlas), protein interactions databases such as HPRD (http://hprd.org/), KEGG biochemical reactions (http://www.genome.jp/kegg/), Interactome (http://interactome.org/), sequenced tumor genomes, including gliomas and glioblastomas (https://cghub.ucsc.edu/). The Allen Institute has developed the Ivy Glioblastoma Atlas Project database (http://glioblastoma.alleninstitute.org/) according to patients with glioma. We demonstrate that these publicly available online bioinformatics tools can give helpful information for annotation of gene list for glioblastoma, reconstruction of gene network and comparative analysis of the related diseases. This approach for gene network analysis of list of gene names using online bioinformatics tools presents application of bioinformatics methods to annotation of complex human diseases. We used DAVID (Database for Annotation, Visualization and Integrated Discovery) tool (https://david.ncifcrf.gov/summary.jsp) and the PANTHER (Protein ANalysis THrough Evolutionary Relationships) (http://pantherdb.org/) resource for gene ontology analysis. Then we applied gene network reconstruction tools. Prioritization of genes was performed using the resource ToppGene: Candidate gene prioritization (https://toppgene.cchmc.org).