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pmid:40613560

Decoding PANoptosis in Gout: Signature Gene Identification and Immune Infiltration Profiling.

Junjie Cao · Aifang Li · Gaiying Luo · Zhen Wu · Yuan Liu

International journal of rheumatic diseases · 2025 doi:10.1111/1756-185X.70344

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complete

Experiment

complete

Data

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Decoding PANoptosis in Gout: Signature Gene Identification and Immune Infiltration Profiling.
doi
10.1111/1756-185X.70344
pmid
40613560
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Junjie Cao
[1]
Aifang Li
[2]
Gaiying Luo
[3]
Zhen Wu
[4]
Yuan Liu
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International journal of rheumatic diseases
year
2025
abstract
BACKGROUND: Gout is an inflammatory disorder triggered by the deposition of monosodium urate (MSU) crystals in joints and periarticular tissues. PANoptosis, a recently identified form of inflammatory cell death, remains uncharacterized in gout pathogenesis. This study aims to identify PANoptosis-related genes that may drive gout progression. METHODS: Gout-related datasets, including the human cohort (GSE160170) and murine model (GSE190138), were retrieved from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were screened using thresholds of |log2 fold change (FC)| ≥ 1 and adjusted P-value < 0.05. PANoptosis-related biomarkers were identified through the combined use of MCODE and cytoHubba algorithms in Cytoscape. Least Absolute Shrinkage and Selection Operator (LASSO) regression was applied to select hub genes. Subsequently, we performed single-sample gene set enrichment analysis (ssGSEA) for the hub genes, analyzed the infiltration levels of immune cells, constructed a miRNA-mRNA-transcription factor (TF) regulatory network, and identified potential therapeutic drugs via the DSigDB database and the Coremine Medical database. Finally, the expression of the diagnostic gene was validated by real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR). RESULTS: The PANoptosis-associated gene SOCS3 was identified via integrative bioinformatics screening. Enrichment analysis and immune infiltration assessment revealed its involvement in gout pathogenesis through pathways linked to inflammation and cell death, with significant correlations observed with specific immune cell subsets. Clinical validation via RT-qPCR confirmed a strong consistency between SOCS3 expression levels in gout patients and computational predictions. CONCLUSION: We identified the hub gene SOCS3 in gout and elucidated its mechanistic roles by integrated bioinformatics analysis, machine learning approach, and clinical validation, providing critical insights for advancing diagnostic biomarkers and therapeutic strategies in gout management.
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rse transcription polymerase chain reaction (RT-qPCR). RESULTS: The PANoptosis-associated gene SO
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immune cell subsets. Clinical validation via RT-qPCR confirmed a strong consistency between SOCS3
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Complete file
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PANoptosis, a recently identified form of inflammatory cell death, remains uncharacterized in gout pathogenesis. This study aims to identify PANoptosis-related genes that may drive gout progression.\nMETHODS: Gout-related datasets, including the human cohort (GSE160170) and murine model (GSE190138), were retrieved from the Gene Expression Omnibus (GEO) database. Differentially expressed genes (DEGs) were screened using thresholds of |log2 fold change (FC)| ≥ 1 and adjusted P-value < 0.05. PANoptosis-related biomarkers were identified through the combined use of MCODE and cytoHubba algorithms in Cytoscape. Least Absolute Shrinkage and Selection Operator (LASSO) regression was applied to select hub genes. Subsequently, we performed single-sample gene set enrichment analysis (ssGSEA) for the hub genes, analyzed the infiltration levels of immune cells, constructed a miRNA-mRNA-transcription factor (TF) regulatory network, and identified potential therapeutic drugs via the DSigDB database and the Coremine Medical database. Finally, the expression of the diagnostic gene was validated by real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR).\nRESULTS: The PANoptosis-associated gene SOCS3 was identified via integrative bioinformatics screening. Enrichment analysis and immune infiltration assessment revealed its involvement in gout pathogenesis through pathways linked to inflammation and cell death, with significant correlations observed with specific immune cell subsets. Clinical validation via RT-qPCR confirmed a strong consistency between SOCS3 expression levels in gout patients and computational predictions.\nCONCLUSION: We identified the hub gene SOCS3 in gout and elucidated its mechanistic roles by integrated bioinformatics analysis, machine learning approach, and clinical validation, providing critical insights for advancing diagnostic biomarkers and therapeutic strategies in gout management.", "claims": [{"id": "claim-method", "statement": "The R package “glmnet” was utilized to further screen candidate genes for gout diagnosis through LASSO‐Cox regression analysis.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40613560", "locator": "sections[8] \"LASSO Regression Model\" paragraph 2", "quote": "The R package “glmnet” was utilized to further screen candidate genes for gout diagnosis through LASSO‐Cox regression analysis."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data that support the findings of this study are available from the corresponding author upon reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40613560", "locator": "sections[30] \"Data Availability Statement\" paragraph 2", "quote": "The data that support the findings of this study are available from the corresponding author upon reasonable request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The PANoptosis-associated gene SOCS3 was identified via integrative bioinformatics screening.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:40613560", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The PANoptosis‐associated gene SOCS3 was identified via integrative bioinformatics screening."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The PANoptosis-associated gene SOCS3 was identified via integrative bioinformatics screening.", "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:40613560"], "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. 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