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pmid:38886500

Regulatory network analysis based on integrated miRNA-TF reveals key genes in heart failure.

Ziyue Zhang · Ziying Zou · Hui Zhang · Dai-Min Zhang

Scientific reports · 2024 doi:10.1038/s41598-024-64732-y

Paper

complete

Experiment

complete

Data

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Analysis

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Regulatory network analysis based on integrated miRNA-TF reveals key genes in heart failure.
doi
10.1038/s41598-024-64732-y
pmid
38886500
authors array · 4 items
[0]
Ziyue Zhang
[1]
Ziying Zou
[2]
Hui Zhang
[3]
Dai-Min Zhang
journal
Scientific reports
year
2024
abstract
The etiology and pathophysiology of heart failure are still unknown. Increasing evidence suggests that abnormal microRNAs (miRNAs) and transcription factors (TFs) expression may be associated with the development of heart failure. Therefore, this study aims to explore key miRNAs, TFs, and related genes in heart failure to gain a greater understanding of the pathogenesis of heart failure. To search and download the dataset of mRNA chips related to heart failure from the GEO database (GSE59867, GSE9128, and GSE134766), we analyzed differential genes and screened the common differentially expressed genes on two chips using R language software. The binary interactions and circuits among miRNAs, TFs, and corresponding genes were determined by Pearson correlation coefficient. A regulatory network of miRNAs, TFs, and target genes was constructed based on bioinformatics. By comparing the sequences of patients with and without heart failure, five downregulated genes with hypermethylated mRNA and three upregulated genes with hypomethylated mRNA were identified. The miRNA-TF gene regulatory network consisted of 26 miRNAs, 22 TFs and six genes. GO and KEGG analysis results revealed that BP terms like cellular response to organic substance, cellular response to cytokine stimulus, and KEGG pathways like osteoclast differentiation, MAPK signaling pathway, and legionellosis were enriched of the DEGs. TMEM87A, PPP2R2A, DUSP1, and miR-92a have great potential as biomarkers for heart failure. The integrated analysis of the mRNA expression spectrum and microRNA-transcription factor-gene revealed the regulatory network of heart failure, which may provide clues to its alternative treatment.
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The empirical Bayes method in limma package was used to screen DEGs with the screening threshold as the corrected P-value < 0.05 and | logFC |≥ 1.
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The empirical Bayes method in limma package was used to screen DEGs with the screening threshold as the corrected P-value < 0.05 and | logFC |≥ 1.
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Publicly available datasets were analyzed in this study. This data can be found here: Gene Expression Omnibus: GSE59867, GSE9128, GSE134766. Data is provided within the manuscript or supplementary information files.
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Publicly available datasets were analyzed in this study. This data can be found here: Gene Expression Omnibus: GSE59867, GSE9128, GSE134766. Data is provided within the manuscript or supplementary information files.
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TMEM87A, PPP2R2A, DUSP1, and miR-92a have great potential as biomarkers for heart failure.
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TMEM87A, PPP2R2A, DUSP1, and miR-92a have great potential as biomarkers for heart failure.
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TMEM87A, PPP2R2A, DUSP1, and miR-92a have great potential as biomarkers for heart failure.
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sample_count
436
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platform
6244
taxon
Homo sapiens
title
Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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data:geo:GSE9128
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Publicly available datasets were analyzed in this study. This data can be found here: Gene Expression Omnibus: GSE59867, GSE9128, GSE134766. Data is provided within the manuscript or supplementary information files.
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Publicly available datasets were analyzed in this study. This data can be found here: Gene Expression Omnibus: GSE59867, GSE9128, GSE134766. Data is provided within the manuscript or supplementary information files.
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sample_count
11
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null
platform
96
taxon
Homo sapiens
title
Expression data from heart failure vs control peripheral blood mononuclear cells.
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2026-11-01T18:06:44Z
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identifier_resolution_only_no_download_no_licence_read
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The empirical Bayes method in limma package was used to screen DEGs with the screening threshold as the corrected P-value < 0.05 and | logFC |≥ 1.
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evidence object · 3 fields
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capability object · 3 fields
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Automated Assays Laravel application and simulated adapters
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The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
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Publicly available datasets were analyzed in this study. This data can be found here: Gene Expression Omnibus: GSE59867, GSE9128, GSE134766. Data is provided within the manuscript or supplementary information files.
basis
The paper names GSE59867, GSE9128, GSE134766 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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minimax
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minimax
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independence
single_reader
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:38886500", "kind": "science-record", "revision": 4, "content_hash": "sha256:95263f9f55c173e0846dec8b5db753f498b1dcc187f4c4bedc288ca6634e4889", "created_at": "2026-11-01T20:28:57Z", "updated_at": "2026-11-01T22:54:30Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Regulatory network analysis based on integrated miRNA-TF reveals key genes in heart failure.", "doi": "10.1038/s41598-024-64732-y", "pmid": "38886500", "authors": ["Ziyue Zhang", "Ziying Zou", "Hui Zhang", "Dai-Min Zhang"], "journal": "Scientific reports", "year": 2024, "abstract": "The etiology and pathophysiology of heart failure are still unknown. Increasing evidence suggests that abnormal microRNAs (miRNAs) and transcription factors (TFs) expression may be associated with the development of heart failure. Therefore, this study aims to explore key miRNAs, TFs, and related genes in heart failure to gain a greater understanding of the pathogenesis of heart failure. To search and download the dataset of mRNA chips related to heart failure from the GEO database (GSE59867, GSE9128, and GSE134766), we analyzed differential genes and screened the common differentially expressed genes on two chips using R language software. The binary interactions and circuits among miRNAs, TFs, and corresponding genes were determined by Pearson correlation coefficient. A regulatory network of miRNAs, TFs, and target genes was constructed based on bioinformatics. By comparing the sequences of patients with and without heart failure, five downregulated genes with hypermethylated mRNA and three upregulated genes with hypomethylated mRNA were identified. The miRNA-TF gene regulatory network consisted of 26 miRNAs, 22 TFs and six genes. GO and KEGG analysis results revealed that BP terms like cellular response to organic substance, cellular response to cytokine stimulus, and KEGG pathways like osteoclast differentiation, MAPK signaling pathway, and legionellosis were enriched of the DEGs. TMEM87A, PPP2R2A, DUSP1, and miR-92a have great potential as biomarkers for heart failure. 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