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摘要
Glioblastoma is the most prevalent malignant glioma in WHO grade IV and its median overall survival is 12-15 months. This study identifies the primary glioblastoma. prognostic genes. Gene expression data in primary glioblastomas with short-term (<12 months, N=16), intermediate (12-36 months, N=31), and long-term (>36 months, N=23) overall survival wore downloaded from Gene Expression Omnibus (GSE53733). Limma determined the differentially expressed genes (DEGs) between different groups (|log2 fold change| >0.5 and p-value <0.05). STRING database and Cytoscape were used to predict protein-protein interactions between DEGs and to construct the PPI network (PPI, medium confidence >= 0.4), and CytoNCA plugin in Cytoscape calculated each DEG's degree, betweenness, sub-graph and closeness centralities. Long-term/ short-term survival-related DEGs were defined as those with increased/decreased expression values and survival time. The following DEGs were identified; 161 between intermediate and short-term glioblastomas, 465 betwoen long-term and short-term and 624 betwoen long-term and intermediate tumors. Hie common FLRT1 and LINGO1 up-regulated DEGs and common down-regulated C7orf31 were identified in these three DEG sets. PPI networks wore established, and VEGFA was the key DEG in each PPI network. The short-term survival-related DEGs were enriched in 3 cancer-related pathways. Moreover, FLRTl and LINGO1 were long-term survival-related DEGs and C7orf31 and VEGFA were short-term survival DEGs. LINGO1, C7orf31, and VEGFA wore confirmed using a further dataset, and we therefore conclude that LINGO1 might be a positive primary glioblastoma prognostic gene and C7orf31 and VEGFA might be negative prognosticators.
- 出版日期2018
- 单位山东大学; 济南市中心医院
