Comprehensive Analyses of miRNA-mRNA Network and Potential Drugs in Idiopathic Pulmonary Arterial Hypertension

Abstract EN

Introduction.

Idiopathic pulmonary arterial hypertension (IPAH) is a severe cardiopulmonary disease with a relatively low survival rate.

Moreover, the pathogenesis of IPAH has not been fully recognized.

Thus, comprehensive analyses of miRNA-mRNA network and potential drugs in IPAH are urgent requirements.

Methods.

Microarray datasets of mRNA and microRNA (miRNA) in IPAH were searched and downloaded from Gene Expression Omnibus (GEO).

Differentially expressed genes (DEGs) and differentially expressed miRNAs (DEMIs) were identified.

Then, the DEMI-DEG network was conducted with associated comprehensive analyses including Gene Ontology (GO) analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and protein-protein interaction (PPI) network analysis, while potential drugs targeting hub genes were investigated using L1000 platform.

Results.

30 DEGs and 6 DEMIs were identified in the lung tissue of IPAH.

GO and KEGG pathway analyses revealed that these DEGs were mostly enriched in antimicrobial humoral response and African trypanosomiasis, respectively.

The DEMI-DEG network was conducted subsequently with 4 DEMIs (hsa-miR-34b-5p, hsa-miR-26b-5p, hsa-miR-205-5p, and hsa-miR-199a-3p) and 16 DEGs, among which 5 DEGs (AQP9, SPP1, END1, VCAM1, and SAA1) were included in the top 10 hub genes of the PPI network.

Nimodipine was identified with the highest CMap connectivity score in L1000 platform.

Conclusion.

Our study conducted a miRNA-mRNA network and identified 4 miRNAs as well as 5 mRNAs which may play important roles in the pathogenesis of IPAH.

Moreover, we provided a new insight for future therapies by predicting potential drugs targeting hub genes.