Key result
Analysis identifies 10 hub genes regulating post-MI ventricular remodeling in non-infarcted myocardium.
Why the study?
There are few diagnostic and therapeutic targets for myocardial remodeling in the salvageable non-infarcted myocardium.
Identifies 10 hub genes that may serve as novel therapeutic targets for mitigating adverse ventricular remodeling in non-infarcted myocardium following AMI.
Answers are grounded in this paper and cite their sources.
Hub genes may nominate targets for post-MI remodeling; leaves open validation and translation in human studies.
(1) Background: There are few diagnostic and therapeutic targets for myocardial remodeling in the salvageable non-infarcted myocardium. (2) Methods: Hub genes were identified through comprehensive bioinformatics analysis (GSE775, GSE19322, and GSE110209 from the gene expression omnibus (GEO) database) and the biological functions of hub genes were examined by gene ontology (GO) functional enrichment and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment. Furthermore, the differential expression of hub genes in various cell populations between the acute myocardial infarction (AMI) and sham-operation groups was analyzed by processing scRNA data (E-MTAB-7376 from the ArrayExpress database) and RNA-seq data (GSE183168). (3) Results: Ten strongly interlinked hub genes (Timp1, Sparc, Spp1, Tgfb1, Decr1, Vim, Serpine1, Serpina3n, Thbs2, and Vcan) were identified by the construction of a protein–protein interaction network from 135 differentially expressed genes identified through comprehensive bioinformatics analysis and their reliability was verified using GSE119857. In addition, the 10 hub genes were found to influence the ventricular remodeling of non-infarcted tissue by modulating the extracellular matrix (ECM)-mediated myocardial fibrosis, macrophage-driven inflammation, and fatty acid metabolism. (4) Conclusions: Ten hub genes were identified, which may provide novel potential targets for the improvement and treatment of AMI and its complications.
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Wang et al. (2022) studied Myocardial remodeling following acute myocardial infarction (n=27). Acute myocardial infarction vs. Sham operation was evaluated on Identification of differentially expressed hub genes. Ten hub genes (Timp1, Sparc, Spp1, Tgfb1, Decr1, Vim, Serpine1, Serpina3n, Thbs2, and Vcan) were identified as key regulators of ventricular remodeling in the non-infarcted myocardium following acute myocardial infarction.
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