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pmid:41472944

Identification and Analysis of PANoptosis Associated with Coronary Artery Disease Using Integrated Bioinformatics Methods.

Yu Liu · Ziyuan Wang · Zhichao Ye · Enjie Zhou · Yifan Wang

Iranian journal of biotechnology · 2026 doi:10.30498/ijb.2025.507255.4080

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complete

Experiment

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Data

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pmid:41472944
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title
Identification and Analysis of PANoptosis Associated with Coronary Artery Disease Using Integrated Bioinformatics Methods.
doi
10.30498/ijb.2025.507255.4080
pmid
41472944
authors array · 5 items
[0]
Yu Liu
[1]
Ziyuan Wang
[2]
Zhichao Ye
[3]
Enjie Zhou
[4]
Yifan Wang
journal
Iranian journal of biotechnology
year
2026
abstract
Background: Coronary artery disease (CAD) is the leading cause of death in the world. Traditional imaging diagnostic techniques are difficult to be popularized due to the limitations of equipment and technical threshold. PANoptosis, as a synergistic integration form of apoptosis, necroptosis and pyroptosis, regulates multiple death pathways through PANoptosome complex, which is closely related to inflammation and organ damage. Objective: This study aims to integrate bioinformatics methods, comprehensively analyze the association between CAD and PANoptosis, and screen the key diagnostic markers. Materials and Methods: Three gene chip datasets (GSE12288, GSE20680 and GSE20681) were obtained from the GEO database, and 7 PANoptosis related differentially expressed genes (PRDEGs) were identified by Venn diagram overlap analysis to construct a CAD diagnostic model. The functional enrichment analysis of these PRDEGs was performed, and human umbilical vein endothelial cells (HUVEC) were used for in vitro functional verification. Results: FADD, PSTPIP2 and CASP8 were the core regulatory genes of CAD, and the logistic regression model based on three genes showed the best diagnostic efficiency (AUC=0.92). PRDEGs were mainly enriched in inflammatory factor signaling pathway, cell necrosis and pyroptosis pathway. Overexpression of FADD/CASP8 inhibited HUVEC proliferation and promoted apoptosis, while PSTPIP2 showed the opposite effect. Conclusion: This study reveals the molecular network of PANoptosis in CAD, and the constructed FADD-PSTPIP2-CASP8 diagnostic model provides a new tool for non-invasive screening.
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The R limma package was used to identify DEGs between the CAD group and the corresponding control groups.
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sample_count
198
group_sizes
null
group_sizes_basis
null
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4133
taxon
Homo sapiens
title
Whole Blood Cell Gene Expression Profiling in Patients with Coronary Artery Disease from the PREDICT Trial
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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The R limma package was used to identify DEGs between the CAD group and the corresponding control groups.
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specific
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data object · 6 fields
tier
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statements array · 1 item
[0]
The Datasets (GSE12288, GSE20680, and GSE20681) in this study are obtained from GEO database (www.ncbi.nlm.nih.gov/geo).
basis
The paper names GSE12288, GSE20680, GSE20681 in GEO database 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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[0]
ptosis, as a synergistic integration form of apoptosis, necroptosis and pyroptosis, regulates multi
[1]
8 inhibited HUVEC proliferation and promoted apoptosis, while PSTPIP2 showed the opposite effect. C
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41472944", "kind": "science-record", "revision": 4, "content_hash": "sha256:12adf6a4cac8504543c47d377eac3771f7b7ad25701e84d5e0a3f7aa4cd197b8", "created_at": "2026-11-01T20:31:27Z", "updated_at": "2026-11-01T22:57:40Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification and Analysis of PANoptosis Associated with Coronary Artery Disease Using Integrated Bioinformatics Methods.", "doi": "10.30498/ijb.2025.507255.4080", "pmid": "41472944", "authors": ["Yu Liu", "Ziyuan Wang", "Zhichao Ye", "Enjie Zhou", "Yifan Wang"], "journal": "Iranian journal of biotechnology", "year": 2026, "abstract": "Background: Coronary artery disease (CAD) is the leading cause of death in the world. Traditional imaging diagnostic techniques are difficult to be popularized due to the limitations of equipment and technical threshold. PANoptosis, as a synergistic integration form of apoptosis, necroptosis and pyroptosis, regulates multiple death pathways through PANoptosome complex, which is closely related to inflammation and organ damage.\nObjective: This study aims to integrate bioinformatics methods, comprehensively analyze the association between CAD and PANoptosis, and screen the key diagnostic markers.\nMaterials and Methods: Three gene chip datasets (GSE12288, GSE20680 and GSE20681) were obtained from the GEO database, and 7 PANoptosis related differentially expressed genes (PRDEGs) were identified by Venn diagram overlap analysis to construct a CAD diagnostic model. The functional enrichment analysis of these PRDEGs was performed, and human umbilical vein endothelial cells (HUVEC) were used for in vitro functional verification.\nResults: FADD, PSTPIP2 and CASP8 were the core regulatory genes of CAD, and the logistic regression model based on three genes showed the best diagnostic efficiency (AUC=0.92). PRDEGs were mainly enriched in inflammatory factor signaling pathway, cell necrosis and pyroptosis pathway. Overexpression of FADD/CASP8 inhibited HUVEC proliferation and promoted apoptosis, while PSTPIP2 showed the opposite effect.\nConclusion: This study reveals the molecular network of PANoptosis in CAD, and the constructed FADD-PSTPIP2-CASP8 diagnostic model provides a new tool for non-invasive screening.", "claims": [{"id": "claim-method", "statement": "The R limma package was used to identify DEGs between the CAD group and the corresponding control groups.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41472944", "locator": "sections[5] \"3.2. 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This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE12288"], "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:GSE12288"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:41472944", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.30498/ijb.2025.507255.4080", "sha256": "sha256:ea0ec762c2665543227b8895a832d8b2dc987829020a1f030a1fa90a7a913b37", "bytes": 55118, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.30498/ijb.2025.507255.4080", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC12745712", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE12288", "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=GSE12288", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE12288", "version": null, "note": "The Datasets (GSE12288, GSE20680, and GSE20681) in this study are obtained from GEO database (www.ncbi.nlm.nih.gov/geo).", 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