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pmid:32460775

Identification of transcription factors MYC and C/EBPβ mediated regulatory networks in heart failure based on gene expression omnibus datasets.

Haiwei Wang · Xinrui Wang · Liangpu Xu · Hua Cao

BMC cardiovascular disorders · 2020 doi:10.1186/s12872-020-01527-9

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complete

Experiment

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:32460775
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title
Identification of transcription factors MYC and C/EBPβ mediated regulatory networks in heart failure based on gene expression omnibus datasets.
doi
10.1186/s12872-020-01527-9
pmid
32460775
authors array · 4 items
[0]
Haiwei Wang
[1]
Xinrui Wang
[2]
Liangpu Xu
[3]
Hua Cao
journal
BMC cardiovascular disorders
year
2020
abstract
BACKGROUND: Heart failure is one of leading cause of death worldwide. However, the transcriptional profiling of heart failure is unclear. Moreover, the signaling pathways and transcription factors involving the heart failure development also are largely unknown. Using published Gene Expression Omnibus (GEO) datasets, in the present study, we aim to comprehensively analyze the differentially expressed genes in failing heart tissues, and identified the critical signaling pathways and transcription factors involving heart failure development. METHODS: The transcriptional profiling of heart failure was identified from previously published gene expression datasets deposited in GSE5406, GSE16499 and GSE68316. The enriched signaling pathways and transcription factors were analyzed using Database for Annotation, Visualization and Integrated Discovery (DAVID) website and gene set enrichment analysis (GSEA) assay. The transcriptional networks were created by Cytoscape. RESULTS: Compared with the normal heart tissues, 90 genes were particularly differentially expressed in failing heart tissues, and those genes were associated with multiple metabolism signaling pathways and insulin signaling pathway. Metabolism and insulin signaling pathway were both inactivated in failing heart tissues. Transcription factors MYC and C/EBPβ were both negatively associated with the expression profiling of failing heart tissues in GSEA assay. Moreover, compared with normal heart tissues, MYC and C/EBPβ were down regulated in failing heart tissues. Furthermore, MYC and C/EBPβ mediated downstream target genes were also decreased in failing heart tissues. MYC and C/EBPβ were positively correlated with each other. At last, we constructed MYC and C/EBPβ mediated regulatory networks in failing heart tissues, and identified the MYC and C/EBPβ target genes which had been reported involving the heart failure developmental progress. CONCLUSIONS: Our results suggested that metabolism pathways and insulin signaling pathway, transcription factors MYC and C/EBPβ played critical roles in heart failure developmental progress.
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Statistical analysis was performed using the two-tailed paired Student’s t test using R software.
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The datasets used and analyzed during the current study are available from the corresponding author on reasonable request. Accession numbers of the datasets used in current study are GSE5406, GSE16499 and GSE68316 in Gene Expression Omnibus.
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source:pmid:32460775
agent
agent:minimax-reader
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activity-resolve-GSE16499
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accession_resolution
used array · 1 item
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data:geo:GSE16499
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agent:corpus-assay-engine
agents array · 2 items
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id
agent:corpus-assay-engine
type
software
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id
agent:minimax-reader
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source_run_id
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dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
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gaps array · 11 items
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asset:data:geo:GSE16499 licence not read
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[2]
asset:data:geo:GSE5406 licence not read
[3]
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[4]
asset:data:geo:GSE68316 licence not read
[5]
asset:data:geo:GSE68316 not downloaded
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pathway_enrich
support_state
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f2132e96ae6c7a4e
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:32460775", "kind": "science-record", "revision": 6, "content_hash": "sha256:589a44c041fc1db429af65af73cd2a093ceee794bec200da8c80b3a650666dda", "created_at": "2026-11-01T15:41:02Z", "updated_at": "2026-11-01T21:23:17Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of transcription factors MYC and C/EBPβ mediated regulatory networks in heart failure based on gene expression omnibus datasets.", "doi": "10.1186/s12872-020-01527-9", "pmid": "32460775", "authors": ["Haiwei Wang", "Xinrui Wang", "Liangpu Xu", "Hua Cao"], "journal": "BMC cardiovascular disorders", "year": 2020, "abstract": "BACKGROUND: Heart failure is one of leading cause of death worldwide. However, the transcriptional profiling of heart failure is unclear. Moreover, the signaling pathways and transcription factors involving the heart failure development also are largely unknown. Using published Gene Expression Omnibus (GEO) datasets, in the present study, we aim to comprehensively analyze the differentially expressed genes in failing heart tissues, and identified the critical signaling pathways and transcription factors involving heart failure development.\nMETHODS: The transcriptional profiling of heart failure was identified from previously published gene expression datasets deposited in GSE5406, GSE16499 and GSE68316. The enriched signaling pathways and transcription factors were analyzed using Database for Annotation, Visualization and Integrated Discovery (DAVID) website and gene set enrichment analysis (GSEA) assay. The transcriptional networks were created by Cytoscape.\nRESULTS: Compared with the normal heart tissues, 90 genes were particularly differentially expressed in failing heart tissues, and those genes were associated with multiple metabolism signaling pathways and insulin signaling pathway. Metabolism and insulin signaling pathway were both inactivated in failing heart tissues. Transcription factors MYC and C/EBPβ were both negatively associated with the expression profiling of failing heart tissues in GSEA assay. Moreover, compared with normal heart tissues, MYC and C/EBPβ were down regulated in failing heart tissues. Furthermore, MYC and C/EBPβ mediated downstream target genes were also decreased in failing heart tissues. MYC and C/EBPβ were positively correlated with each other. At last, we constructed MYC and C/EBPβ mediated regulatory networks in failing heart tissues, and identified the MYC and C/EBPβ target genes which had been reported involving the heart failure developmental progress.\nCONCLUSIONS: Our results suggested that metabolism pathways and insulin signaling pathway, transcription factors MYC and C/EBPβ played critical roles in heart failure developmental progress.", "claims": [{"id": "claim-method", "statement": "Statistical analysis was performed using the two-tailed paired Student’s t test using R software.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:32460775", "locator": "sections[11] \"Statistical analysis\" paragraph 2", "quote": "Statistical analysis was performed using the two-tailed paired Student’s t test using R software."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The datasets used and analyzed during the current study are available from the corresponding author on reasonable request. 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Accession numbers of the datasets used in current study are GSE5406, GSE16499 and GSE68316 in Gene Expression Omnibus."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:32460775"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE16499"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE16499"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:32460775", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s12872-020-01527-9", "sha256": "sha256:ce2cde7e2951a81cc00e82a7e185e6a06e4a505284b041109d5130a5efb7c0b3", "bytes": 25036, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1186/s12872-020-01527-9", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC7251862", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE16499", "role": "raw", "format": "geo-series", "media_type": "application/vnd.ncbi.geo-series+json", "uri": "https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE16499", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE16499", "version": null, "note": "The datasets used and analyzed during the current study are available from the corresponding author on reasonable request. Accession numbers of the datasets used in current study are GSE5406, GSE16499 and GSE68316 in Gene Expression Omnibus.", "structure": {"repository": "GEO", "access_route": "GEO accession URL", "access_statement_verbatim": "The datasets used and analyzed during the current study are available from the corresponding author on reasonable request. 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