Evidence map›Paper›PMID 42310773›Full record

ArticleJournal of cardiothoracic surgery2026

Identification of PANoptosis-related hub genes in acute myocardial infarction: diagnostic potential, immune correlates, and therapeutic insights.

Xuebing Wang, Xunli Yin, Linlin Teng, Dong Tao

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Article in Journal of cardiothoracic surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xuebing WangDepartment of Cardiovascular Medicine, The Seventh People's Hospital of Jinan, No. 21, Gongyebei Road, Licheng District, Shandong, 250100, Jinan, P.R. China.
Xunli YinDepartment of Cardiovascular Medicine, The Seventh People's Hospital of Jinan, No. 21, Gongyebei Road, Licheng District, Shandong, 250100, Jinan, P.R. China.
Linlin TengDepartment of Cardiovascular Medicine, The Seventh People's Hospital of Jinan, No. 21, Gongyebei Road, Licheng District, Shandong, 250100, Jinan, P.R. China.
Dong TaoDepartment of Cardiovascular Medicine, The Seventh People's Hospital of Jinan, No. 21, Gongyebei Road, Licheng District, Shandong, 250100, Jinan, P.R. China. 15688875136@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPANoptosis is an innate immune-inflammatory programmed cell death pathway that integrates the key features of apoptosis, pyroptosis, and necroptosis. However, the diagnostic potential and immune relevance of PANoptosis-related genes in acute myocardial infarction (AMI) remain unclear.

methodsTranscriptional data were obtained from the GEO database, including the training set GSE66360 and validation set GSE59867. Differential expression, protein-protein interaction networks, and random forest analyses were conducted to identify PANoptosis-related hub genes associated with AMI pathogenesis. The diagnostic model and nomogram were built, and the diagnostic value was evaluated using receiver operating characteristic analysis. Immune infiltration, functional enrichment, and regulatory network analyses were performed to explore potential molecular mechanisms. Blood samples from healthy controls and AMI patients were collected to validate the expression of hub genes.

resultsA total of 438 DEGs and 109 PANoptosis-related genes were obtained. After intersecting these, 8 PANoptosis genes associated with AMI were found, enriched in apoptosis, immune, and inflammatory pathways. Two hub genes, IL1B and NLRP3, were identified as hub genes, with diagnostic models and nomograms showing good performance in both training and validation sets. These genes were significantly correlated with most immune cells that were dysregulated in AMI, revealing their immunomodulatory function. CEBPB and SPI1 were identified as common transcriptional regulators of the hub genes. Five drugs associated with hub genes were predicted from the DSigDB database. IL1B and NLRP3 showed consistent expression patterns across the training set, validation set, and real-time qPCR analysis.

conclusionIL1B and NLRP3 may serve as PANoptosis-related biomarkers with potential immunomodulation in AMI, offering preliminary insights into the potential molecular mechanisms of PANoptosis in AMI.

trial registrationNot applicable.

Indexed as

Interleukin-1betaMyocardial InfarctionNLR Family, Pyrin Domain-Containing 3 ProteinApoptosisGene Expression ProfilingHumansIL1B protein, humanInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanAcute myocardial infarctionDiagnostic biomarkersInterleukin 1 beta (IL1B)NOD-like receptor family pyrin domain containing 3 (NLRP3)PANoptosis

Identifiers

PMID42310773
PMCPMC13459456

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.