Fig. 3From: Metabolic control of PPAR activity by aldehyde dehydrogenase regulates invasive cell behavior and predicts survival in hepatocellular and renal clear cell carcinomaPathway and gene set enrichment analysis. a Workflow of pathway and gene set enrichment analysis between ALDH7A1 high and low expression groups of LIHC and KIRC patients. Low expressed genes were filtered out by requiring RSEM >ā10 in >ā33% of patients. Genes differentially expressed between the low and high ALDH7A1 mRNA tumor groups were selected using a minimum threshold of +/āā0.4 log2-fold change, with an adjusted p-value of <ā0.05. Fold change and p-values were used according to requirements of each specific method. Six different R packages (ESEA, GRAPHITE, SPIA, CEPA, PIANO and GAGE) were applied to the Reactome, BioCarta, NCI andĀ KEGG pathway databases and the MsigDB gene set annotation collections, as indicated. b Summary of significantly affected pathways and biological processes after filtering. ā - pathway inactivated /down regulated; ā pathway activated /up regulated, ā - direction not provided. Light blue ā amino acid metabolism; bright red ā PPAR signaling pathway; light violet ā energy metabolism; dark red ā bile acid metabolism; light green ā lipid, fatty acid metabolism; light orange - processes related to cell motility. c Map of the PPAR signaling pathway from the KEGG database, showing genes that were differentially expressed in LIHC tumors with low ALDH7A1 expression. Scale ā log2FC; Blue: lower expression in tumors. Red: higher expression in tumors. Image rendered by Pathview [28]Back to article page