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pmid:41365992

Identification of potential biomarkers associated with mitochondrial oxidative stress in idiopathic pulmonary arterial hypertension via bioinformatic and experimental analysis.

Yanting Zhu · Xiaoming Wang · Xiaohui Yan · Yan Sun · Qiong Wang · Cui Zhai

Scientific reports · 2025 doi:10.1038/s41598-025-31150-7

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complete

Experiment

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Data

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title
Identification of potential biomarkers associated with mitochondrial oxidative stress in idiopathic pulmonary arterial hypertension via bioinformatic and experimental analysis.
doi
10.1038/s41598-025-31150-7
pmid
41365992
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[0]
Yanting Zhu
[1]
Xiaoming Wang
[2]
Xiaohui Yan
[3]
Yan Sun
[4]
Qiong Wang
[5]
Cui Zhai
journal
Scientific reports
year
2025
abstract
Idiopathic pulmonary arterial hypertension (IPAH) is a progressive and devastating disorder. Mitochondrial oxidative stress has been found to be involved in PAH development. This study aims to explore potential mitochondrial oxidative stress-related biomarkers in IPAH via integrated bioinformatics, validate these genes in MCT-induced rat PAH model and examine the functional roles of COX6B1 and HMGCL in mitochondrial oxidative stress in PDGF-induced pulmonary arterial smooth muscle cells (PASMCs). GSE15197 was downloaded from GEO database. Genes associated with mitochondria and oxidative stress were obtained from Molecular Signatures Database and MitoCarta3.0 databases. Weighted gene co-expression network analysis (WGCNA) was used. GO and KEGG enrichment analysis were utilized. Furthermore, machine learning algorithms (LASSO, SVM-RFE and RF) were constructed to screen hub genes. A nomogram model based on the hub genes were performed for evaluation the diagnostic value, and the expression of hub genes were validated by real-time quantitative PCR and Western blot in MCT-induced rat PAH model. Finally, COX6B1 and HMGCL specific siRNAs were transfected into PDGF-induced PASMCs, mitochondrial ROS (mtROS) level and MnSOD activity were examined. A total of 18 genes related to mitochondrial oxidative stress were identified in IPAH. Two hub genes (COX6B1 and HMGCL) were finally determined as potential biomarkers. Based on the 2 genes, a nomogram model was constructed. This model exhibited remarkable diagnostic efficiency values for IPAH. The expressions of COX6B1 and HMGCL were found to be upregulated in MCT-induced PAH model, in agreement with the findings of bioinformatics analysis. While, transfection with either COX6B1 siRNA or HMGCL siRNA suppressed the abnormal accumulation of mtROS and restored MnSOD activity in PDGF-induced PASMCs. Our results indicated that two mitochondrial oxidative stress-related genes (COX6B1 and HMGCL) were identified as diagnostic biomarkers and may serve as potential targets for IPAH development, although further research is necessary.
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Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification.
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sections[13] "Identification of DEGs" paragraph 2
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Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification.
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Datasets (GSE15197) used in the study can be downloaded from the public GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE15197). The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.
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The study identified COX6B1 and HMGCL as mitochondrial oxidative stress-related candidate biomarkers for IPAH, with the two-gene diagnostic model achieving an AUC of 0.974.
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Furthermore, a combined ROC analysis of the 2 hub genes showed an AUC was 0.974, extremely high diagnostic efficiency (Fig. 5C).
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Two hub genes (COX6B1 and HMGCL) were finally determined as potential biomarkers.
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Furthermore, a combined ROC analysis of the 2 hub genes showed an AUC was 0.974, extremely high diagnostic efficiency (Fig. 5C).
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The study identified COX6B1 and HMGCL as mitochondrial oxidative stress-related candidate biomarkers for IPAH, with the two-gene diagnostic model achieving an AUC of 0.974.
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RNA Expression Profiling of Lung Tissue Identifies Mutually Distinct Molecular Signatures in PAH and PH Secondary to IPF
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Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification.
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Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:41365992", "kind": "science-record", "revision": 4, "content_hash": "sha256:fa99811aa39a02f30cc645bf6a55b4b31b0203bb977d5f3c3c7f00933dc49016", "created_at": "2026-11-01T20:31:22Z", "updated_at": "2026-11-01T22:57:35Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Identification of potential biomarkers associated with mitochondrial oxidative stress in idiopathic pulmonary arterial hypertension via bioinformatic and experimental analysis.", "doi": "10.1038/s41598-025-31150-7", "pmid": "41365992", "authors": ["Yanting Zhu", "Xiaoming Wang", "Xiaohui Yan", "Yan Sun", "Qiong Wang", "Cui Zhai"], "journal": "Scientific reports", "year": 2025, "abstract": "Idiopathic pulmonary arterial hypertension (IPAH) is a progressive and devastating disorder. Mitochondrial oxidative stress has been found to be involved in PAH development. This study aims to explore potential mitochondrial oxidative stress-related biomarkers in IPAH via integrated bioinformatics, validate these genes in MCT-induced rat PAH model and examine the functional roles of COX6B1 and HMGCL in mitochondrial oxidative stress in PDGF-induced pulmonary arterial smooth muscle cells (PASMCs). GSE15197 was downloaded from GEO database. Genes associated with mitochondria and oxidative stress were obtained from Molecular Signatures Database and MitoCarta3.0 databases. Weighted gene co-expression network analysis (WGCNA) was used. GO and KEGG enrichment analysis were utilized. Furthermore, machine learning algorithms (LASSO, SVM-RFE and RF) were constructed to screen hub genes. A nomogram model based on the hub genes were performed for evaluation the diagnostic value, and the expression of hub genes were validated by real-time quantitative PCR and Western blot in MCT-induced rat PAH model. Finally, COX6B1 and HMGCL specific siRNAs were transfected into PDGF-induced PASMCs, mitochondrial ROS (mtROS) level and MnSOD activity were examined. A total of 18 genes related to mitochondrial oxidative stress were identified in IPAH. Two hub genes (COX6B1 and HMGCL) were finally determined as potential biomarkers. Based on the 2 genes, a nomogram model was constructed. This model exhibited remarkable diagnostic efficiency values for IPAH. The expressions of COX6B1 and HMGCL were found to be upregulated in MCT-induced PAH model, in agreement with the findings of bioinformatics analysis. While, transfection with either COX6B1 siRNA or HMGCL siRNA suppressed the abnormal accumulation of mtROS and restored MnSOD activity in PDGF-induced PASMCs. Our results indicated that two mitochondrial oxidative stress-related genes (COX6B1 and HMGCL) were identified as diagnostic biomarkers and may serve as potential targets for IPAH development, although further research is necessary.", "claims": [{"id": "claim-method", "statement": "Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41365992", "locator": "sections[13] \"Identification of DEGs\" paragraph 2", "quote": "Differentially expressed genes (DEGs) between IPAH patients and normal controls in GSE15197 dataset were screened using limma package in R software. The fold change (FC) in gene expression was calculated. The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification."}], "state": "complete"}, {"id": "claim-data-access", "statement": "Datasets (GSE15197) used in the study can be downloaded from the public GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE15197). The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:41365992", "locator": "sections[34] \"Data availability\" paragraph 2", "quote": "Datasets (GSE15197) used in the study can be downloaded from the public GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE15197). The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified COX6B1 and HMGCL as mitochondrial oxidative stress-related candidate biomarkers for IPAH, with the two-gene diagnostic model achieving an AUC of 0.974.", "kind": "quantitative", "target": {"value": 0.974, "unit": "auc", "tolerance": null, "source": "Furthermore, a combined ROC analysis of the 2 hub genes showed an AUC was 0.974, extremely high diagnostic efficiency (Fig. 5C)."}, "evidence": [{"asset": "source:pmid:41365992", "locator": "sections[0] \"Abstract\" paragraph 1", "quote": "Two hub genes (COX6B1 and HMGCL) were finally determined as potential biomarkers."}, {"asset": "source:pmid:41365992", "locator": "sections[6] \"Establishment of a diagnostic model of IPAH samples based on hub genes\" paragraph 2", "quote": "Furthermore, a combined ROC analysis of the 2 hub genes showed an AUC was 0.974, extremely high diagnostic efficiency (Fig. 5C)."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified COX6B1 and HMGCL as mitochondrial oxidative stress-related candidate biomarkers for IPAH, with the two-gene diagnostic model achieving an AUC of 0.974.", "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:41365992"], "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:GSE15197"], "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": {"fdr_threshold": "the Benjamini-Hochberg false discovery rate method"}, "inputs": ["data:geo:GSE15197"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:41365992", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1038/s41598-025-31150-7", "sha256": "sha256:92640730333c68f75524f614b05d191e11e5c1982054fbf62d29667591568ac8", "bytes": 49521, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1038/s41598-025-31150-7", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC12800125", "source": "europe_pmc_fulltext", "coverage": "whole_body", "text_hash_scope": "rendered_section_body"}}, {"id": "data:geo:GSE15197", "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=GSE15197", "sha256": null, "bytes": null, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "GSE15197", "version": null, "note": "Datasets (GSE15197) used in the study can be downloaded from the public GEO database (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE15197). 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The p-value was adjusted for multiple testing using the Benjamini-Hochberg false discovery rate (FDR) method. |log2FC| ≥ 0.85 and FDR-adjusted P-value < 0.05 was defined as criteria for DEGs identification."], "order_basis": "consumes_earlier_output", "id": "assay:5"}]}