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pmid:40951447

Identification of Novel Biomarkers Associated with Corticosteroid Resistance in Asthma by Bioinformatics Analysis and Experimental Validation.

Lingling Xuan · Lulu Ren · Wen Zhang · Zhuoling An

Journal of inflammation research · 2025 doi:10.2147/JIR.S527640

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:40951447
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science-record
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2026-11-01T20:31:02Z
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2026-11-01T22:14:42Z
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paper object · 10 fields
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title
Identification of Novel Biomarkers Associated with Corticosteroid Resistance in Asthma by Bioinformatics Analysis and Experimental Validation.
doi
10.2147/JIR.S527640
pmid
40951447
authors array · 4 items
[0]
Lingling Xuan
[1]
Lulu Ren
[2]
Wen Zhang
[3]
Zhuoling An
journal
Journal of inflammation research
year
2025
abstract
Background: Corticosteroid resistance in asthma, marked by reduced glucocorticoid response, is significantly influenced by cigarette smoke (CS). We sought to explore potential novel biomarkers and therapeutic targets associated with CS-induced corticosteroid resistance in asthma. Methods: GSE230048 (related to corticosteroid resistance) and GSE13896 (from CS-exposed macrophages) were obtained from GEO. Initially, we performed differential gene expression analysis and weighted gene co-expression network analysis (WGCNA) to discover key genes involved in corticosteroid resistance in asthma. Gene Ontology (GO) term and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted. Receiver operating characteristic (ROC) analysis was used to assess the diagnostic accuracy of these markers. CIBERSORT was applied to clarify immune cell infiltration. Expression of the key biomarker was validated in asthma patients and asthma murine models. Results: Five overlapping genes upregulated in corticosteroid-resistant asthma patients and smokers' alveolar macrophages were identified. Subsequently, using WGCNA, the most relevant modules were identified and intersected with differentially expressed genes. Tensin 1 (TNS1), ATP-binding cassette subfamily C member 4 (ABCC4), and TNF receptor superfamily member 21 (TNFRSF21) were identified as critical biomarkers for corticosteroid resistance in asthma. ROC analysis showed an AUC of 0.718 for the three-marker combination. Single-cell RNA sequencing confirmed their expression in macrophages from asthmatic patients. Elevated levels of TNS1, ABCC4, TNFRSF21, and M2 macrophage markers (CD301 and CD206) were observed in CS-exposed murine lung tissues and CS condensate-treated Raw264.7 cells. TNS1 knockdown significantly reduced CD301 and CD206 expression, suggesting its role in promoting macrophage M2 polarization. Conclusion: In conclusion, we identified three hub genes (TNS1, ABCC4, and TNFRSF21) associated with CS-induced corticosteroid resistance in asthma. Additionally, TNS1 may be involved in CS-induced corticosteroid resistance in asthma by promoting macrophage M2 polarization.
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We used the online analysis tool GEO2R to screen the differential genes in dataset GSE230048 and dataset GSE13896.
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sections[5] "Identification of Differentially Expressed Genes (DEGs)" paragraph 2
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We used the online analysis tool GEO2R to screen the differential genes in dataset GSE230048 and dataset GSE13896.
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sections[29] "Data Sharing Statement" paragraph 2
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Data are available from the corresponding author on request.
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Differential-expression and weighted gene co-expression analyses identified TNS1, ABCC4, and TNFRSF21 as critical biomarkers associated with cigarette-smoke-induced corticosteroid resistance in asthma.
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sections[0] "Abstract" paragraph 3
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Tensin 1 (TNS1), ATP-binding cassette subfamily C member 4 (ABCC4), and TNF receptor superfamily member 21 (TNFRSF21) were identified as critical biomarkers for corticosteroid resistance in asthma.
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Differential-expression and weighted gene co-expression analyses identified TNS1, ABCC4, and TNFRSF21 as critical biomarkers associated with cigarette-smoke-induced corticosteroid resistance in asthma.
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Smoking-dependent Reprogramming of Alveolar Macrophage Polarization: Implication for Pathogenesis of COPD
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Gene expression profiling of whole blood and peripheral neutrophils from asthma.
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Chronic Cigarette Smoke Exposure Results in Coordinated Methylation and Gene Expression Changes in Human Alveolar Macrophages
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We used the online analysis tool GEO2R to screen the differential genes in dataset GSE230048 and dataset GSE13896.
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Data are available from the corresponding author on request.
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was validated in asthma patients and asthma murine models. Results: Five overlapping genes upre
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CD301 and CD206) were observed in CS-exposed murine lung tissues and CS condensate-treated Raw26
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ients and in Corticosteroid-Resistant Asthma Murine Models Data from the Human Protein Atlas sho
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oid resistance in asthma, OVA-induced asthma mice were exposed to CS as detailed in methods. sRaw w
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C of 0.718 for the three-marker combination. Single-cell RNA sequencing confirmed their expression in macrophages fr
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or the three-marker combination. Single-cell RNA sequencing confirmed their expression in macrophages fr
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d CS condensate-treated Raw264.7 cells. TNS1 knockdown significantly reduced CD301 and CD206 expres
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ed corticosteroid-resistant murine models by RT-qPCR. CS exposure increased TNS1, ABCC4 and TNFRS
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corticosteroid-resistant murine models by RT-qPCR. CS exposure increased TNS1, ABCC4 and TNFRS
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:40951447", "kind": "science-record", "revision": 3, "content_hash": "sha256:25fa610cee47ef8de14bd985176b00cc945cc43d15369d1b0eaa48c3838a3e9c", "created_at": "2026-11-01T20:31:02Z", "updated_at": "2026-11-01T22:14:42Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of Novel Biomarkers Associated with Corticosteroid Resistance in Asthma by Bioinformatics Analysis and Experimental Validation.", "doi": "10.2147/JIR.S527640", "pmid": "40951447", "authors": ["Lingling Xuan", "Lulu Ren", "Wen Zhang", "Zhuoling An"], "journal": "Journal of inflammation research", "year": 2025, "abstract": "Background: Corticosteroid resistance in asthma, marked by reduced glucocorticoid response, is significantly influenced by cigarette smoke (CS). We sought to explore potential novel biomarkers and therapeutic targets associated with CS-induced corticosteroid resistance in asthma.\nMethods: GSE230048 (related to corticosteroid resistance) and GSE13896 (from CS-exposed macrophages) were obtained from GEO. Initially, we performed differential gene expression analysis and weighted gene co-expression network analysis (WGCNA) to discover key genes involved in corticosteroid resistance in asthma. Gene Ontology (GO) term and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were conducted. Receiver operating characteristic (ROC) analysis was used to assess the diagnostic accuracy of these markers. CIBERSORT was applied to clarify immune cell infiltration. Expression of the key biomarker was validated in asthma patients and asthma murine models.\nResults: Five overlapping genes upregulated in corticosteroid-resistant asthma patients and smokers' alveolar macrophages were identified. Subsequently, using WGCNA, the most relevant modules were identified and intersected with differentially expressed genes. Tensin 1 (TNS1), ATP-binding cassette subfamily C member 4 (ABCC4), and TNF receptor superfamily member 21 (TNFRSF21) were identified as critical biomarkers for corticosteroid resistance in asthma. ROC analysis showed an AUC of 0.718 for the three-marker combination. Single-cell RNA sequencing confirmed their expression in macrophages from asthmatic patients. Elevated levels of TNS1, ABCC4, TNFRSF21, and M2 macrophage markers (CD301 and CD206) were observed in CS-exposed murine lung tissues and CS condensate-treated Raw264.7 cells. TNS1 knockdown significantly reduced CD301 and CD206 expression, suggesting its role in promoting macrophage M2 polarization.\nConclusion: In conclusion, we identified three hub genes (TNS1, ABCC4, and TNFRSF21) associated with CS-induced corticosteroid resistance in asthma. Additionally, TNS1 may be involved in CS-induced corticosteroid resistance in asthma by promoting macrophage M2 polarization.", "claims": [{"id": "claim-method", "statement": "We used the online analysis tool GEO2R to screen the differential genes in dataset GSE230048 and dataset GSE13896.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40951447", "locator": "sections[5] \"Identification of Differentially Expressed Genes (DEGs)\" paragraph 2", "quote": "We used the online analysis tool GEO2R to screen the differential genes in dataset GSE230048 and dataset GSE13896."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Data are available from the corresponding author on request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:40951447", "locator": "sections[29] \"Data Sharing Statement\" paragraph 2", "quote": "Data are available from the corresponding author on request."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Differential-expression and weighted gene co-expression analyses identified TNS1, ABCC4, and TNFRSF21 as critical biomarkers associated with cigarette-smoke-induced corticosteroid resistance in asthma.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:40951447", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Tensin 1 (TNS1), ATP-binding cassette subfamily C member 4 (ABCC4), and TNF receptor superfamily member 21 (TNFRSF21) were identified as critical biomarkers for corticosteroid resistance in asthma."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Differential-expression and weighted gene co-expression analyses identified TNS1, ABCC4, and TNFRSF21 as critical biomarkers associated with cigarette-smoke-induced corticosteroid resistance in asthma.", "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:40951447"], "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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