Hepatocellular carcinoma (HCC) is a global health problem with a complex etiology and pathogenesis.Microarray data is increasingly being used as a novel and effective method for cancer pathogenesis analysis. To unravel the potential prognosis of HCC, an integrative study of mRNA and miRNA for HCC was conducted. Two microarray datasets (GSE89377 and GSE101685) and two miRNAs expression pro les (GSE112264 and GSE113740) were obtained from Gene Expression Omnibus (GEO) database. A total of 177 DEGs and 80 DEMs were screened out. Functional enrichment of DEGs was proceeded by Clue GO, including GO and KEGG pathway analysis. These genes were signi cantly enriched in chemical carcinogenesis. PPI network was then established on the STRING platform, and ten hub genes (CDC20, TOP2A, ASPM, NCAPG, AURKA, CYP2E1, HMMR, PRC1, TYMS, and CYP4A11) were visualized via Cytoscape software. Then, a miRNA-target network was established to identify the dysregulated miRNA.A key miRNA (hsa-miR-124-3p) was ltered. Finally, the miRNA-target-transcription factor networks were constructed for hsa-miR-124-3p. The network for hsa-miR-124-3p included two transcription factors (TFs) and ve targets. These identi ed DEGs and DEMs, TFs, targets, and regulatory networks may help advance our understanding the underlying pathogenesis of HCC.