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Correlation between elevated HCLS1 levels and heart failure: A diagnostic biomarker
Chunguang Li1, Li Zhang2, Long Zhang3
1Clinical Lab Center, Beijing Luhe Hospital, Capital Medical University, Beijing, China.
Insights
Hematopoietic cell-specific lyn substrate 1 (HCLS1) is highly expressed in heart failure (HF). This study identifies HCLS1 and other core genes involved in HF pathogenesis, suggesting potential diagnostic markers.
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- Genomics
Background:
- The relationship between hematopoietic cell-specific lyn substrate 1 (HCLS1) expression and heart failure (HF) is not well understood.
- Investigating gene expression patterns in HF can reveal novel insights into disease mechanisms.
Purpose of the Study:
- To explore the correlation between HCLS1 expression and heart failure.
- To identify key genes and pathways involved in the pathogenesis of heart failure.
Main Methods:
- Analysis of heart failure datasets (GSE192886, GSE196656) from the Gene Expression Omnibus (GEO) database.
- Utilized weighted gene co-expression network analysis, protein-protein interaction (PPI) networks, and functional enrichment analysis.
- Screened microRNAs (miRNAs) targeting differentially expressed genes (DEGs) using TargetScan.
Main Results:
- Identified 500 DEGs primarily associated with leukocyte activation, protein phosphorylation, cell adhesion, PI3K Akt, Notch signaling pathways, and right ventricular cardiomyopathy.
- The PPI network highlighted 15 core genes, including HCLS1, FERMT3, and LYN.
- Four genes (EP300, CD53, HCLS1, LYN) showed high expression in HF tissues and were linked to cardiovascular diseases, inflammation, and necrosis.
Conclusions:
- HCLS1 is significantly upregulated in heart failure tissues.
- The identified core genes and pathways offer potential targets for understanding and treating heart failure.
- HCLS1 may serve as a potential biomarker for heart failure.
Abstract:
The correlation between hematopoietic cell-specific lyn substrate 1 (HCLS1) expression levels and heart failure (HF) remains unclear. HF datasets GSE192886 and GSE196656 profiles were generated from GPL24676 and GPL20301 platforms in gene expression omnibus (GEO) database and differentially expressed genes (DEGs) were obtained, which was followed by weighted gene co-expression network analysis, protein-protein interaction (PPI) networks, functional enrichment analysis and comparative toxicogenomics database (CTD) analysis. Heatmaps of gene expression levels were plotted. TargetScan was used to screen miRNAs regulating central DEGs. A total of 500 DEGs were found and mainly concentrated in leukocyte activation, protein phosphorylation, and protein complexes involved in cell adhesion, PI3K Akt signaling pathway, Notch signaling pathway, and right ventricular cardiomyopathy. PPI network identified 15 core genes (HCLS1, FERMT3, CD53, CD34, ITGAL, EP300, LYN, VAV1, ITGAX, LEP, ITGB1, IGF1, MMP9, SMAD2, RAC2). Heatmap shows that 4 genes (EP300, CD53, HCLS1, LYN) are highly expressed in HF tissue samples. We found that 4 genes (EP300, CD53, HCLS1, LYN) were associated with heart diseases, cardiovascular diseases, edema, rheumatoid arthritis, necrosis, and inflammation. HCLS1 is highly expressed in HF and maybe its target.
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