摘要
We performed weighted gene coexpression network analysis （WGCNA） to gain insights into the molecular aspects of hepatocellular carcinoma （HCC）. Raw microarray datasets （including 488 samples） were downloaded from the Gene Expression Omnibus （GEO） website. Data were normalized using the RMA algorithm. We utilized the WGCNA to identify the coexpressed genes （modules） after non-specific filtering. Correlation and survival analyses were conducted using the modules, and gene ontology （GO） enrichment was applied to explore the possible mechanisms. Eight distinct modules were identified by the WGCNA. Pink and red modules were associated with liver function, whereas turquoise and black modules were inversely correlated with tumor staging. Poor outcomes were found in the low expression group in the turquoise module and in the high expression group in the red module. In addition, GO enrichment analysis suggested that inflammation, immune, virus-related, and interferon-mediated pathways were enriched in the turquoise module. Several potential biomarkers, such as cyclin-dependent kinase 1 （CDK1）, topoisomerase 2α （TOP2A）, and serpin peptidase inhibitor clade C （antithrombin） member 1 （SERPINC1）, were also identified. In conclusion, gene signatures identified from the genome-based assays could contribute to HCC stratification. WGCNA was able to identify significant groups of genes associated with cancer prognosis.
We performed weighted gene coexpression network analysis （WGCNA） to gain insights into the molecular aspects of hepatocellular carcinoma （HCC）. Raw microarray datasets （including 488 samples） were downloaded from the Gene Expression Omnibus （GEO） website. Data were normalized using the RMA algorithm. We utilized the WGCNA to identify the coexpressed genes （modules） after non-specific filtering. Correlation and survival analyses were conducted using the modules, and gene ontology （GO） enrichment was applied to explore the possible mechanisms. Eight distinct modules were identified by the WGCNA. Pink and red modules were associated with liver function, whereas turquoise and black modules were inversely correlated with tumor staging. Poor outcomes were found in the low expression group in the turquoise module and in the high expression group in the red module. In addition, GO enrichment analysis suggested that inflammation, immune, virus-related, and interferon-mediated pathways were enriched in the turquoise module. Several potential biomarkers, such as cyclin-dependent kinase 1 （CDK1）, topoisomerase 2α （TOP2A）, and serpin peptidase inhibitor clade C （antithrombin） member 1 （SERPINC1）, were also identified. In conclusion, gene signatures identified from the genome-based assays could contribute to HCC stratification. WGCNA was able to identify significant groups of genes associated with cancer prognosis.
基金
This manuscript was supported by the National Natural Science Foundation of China （No. 81402022） and the Fund of China Scholarship Council （No. 201406280106）.
