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pmid:35710932

Integrated bioinformatics analysis reveals marker genes and immune infiltration for pulmonary arterial hypertension.

Shengxin Tang · Yue Liu · Bin Liu

Scientific reports · 2022 doi:10.1038/s41598-022-14307-6

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

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:35710932
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science-record
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2026-11-01T18:14:41Z
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2026-11-01T22:49:18Z
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title
Integrated bioinformatics analysis reveals marker genes and immune infiltration for pulmonary arterial hypertension.
doi
10.1038/s41598-022-14307-6
pmid
35710932
authors array · 3 items
[0]
Shengxin Tang
[1]
Yue Liu
[2]
Bin Liu
journal
Scientific reports
year
2022
abstract
Pulmonary arterial hypertension (PAH) is a chronic cardiopulmonary syndrome with high pulmonary vascular load and eventually causing RV heart failure even death. However, the mechanism of pulmonary hypertension remains unclear. The purpose of this research is to detect the underlying key genes and potential mechanism of PAH using several bioinformatic methods. The microarrays GSE22356, GSE131793 and GSE168905 were acquired from the GEO. Subsequently, a host of bioinformatics techniques such as DAVID, STRING, R language and Cytoscape were utilized to investigate DEGs between PAH and healthy controls and conduct GO annotation, KEGG enrichment analysis and PPI network construction etc. Additionally, we predicted the transcription factors regulating DEGs through iRegulon plugin of Cytoscape and CIBERSORT was used to conduct immune infiltration analysis. One thousand two hundred and seventy-seven DEGs (403 up-regulated and 874 down-regulated) were identified from peripheral blood samples of 32 PAH patients and 29 controls, among which SLC4A1, AHSP, ALAS2, CA1, HBD, SNCA, HBM, SELENBP1, SERPINE1 and ITGA2B were detected as hub genes. The functional enrichment changes of DEGs were mainly enriched in protein binding, extracellular exosome, extracellular space, extracellular region and integral component of plasma membrane. The hub genes are chiefly enriched at extracellular exosome, hemoglobin complex, blood microparticle, oxygen transporter activity. Among TF-DEGs network, 42 target DEGs and 6 TFs were predicted with an NES > 4 (TEAD4, TGIF2LY, GATA5, GATA1, GATA2, FOS). Immune infiltration analysis showed that monocytes occupied the largest proportion of immune cells. The trend analysis results of infiltration immune cells illustrated that PAH patients had higher infiltration of NK cell activation, monocyte, T cell CD4 memory activation, and mast cell than healthy controls and lower infiltration of T cell CD4 naive. We detected SLC4A1, AHSP, ALAS2, CA1, HBD, SNCA, HBM, SELENBP1, SERPINE1 and ITGA2B as the most significant markers of PAH. The PAH patients had higher infiltration of NK cell activation, monocyte, T cell CD4 memory activation, and mast cell than healthy controls and lower infiltration of T cell CD4 naive. These identified genes and these immune cells probably have precise regulatory relationships in the development of PAH.
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For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21.
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sections[12] "Identification of DEGs" paragraph 2
quote
For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21.
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The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905).
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sections[21] "Data availability" paragraph 2
quote
The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905).
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Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays.
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sections[3] "Identification of DEGs in PAH" paragraph 2
quote
Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays.
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Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays.
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Meta-analysis of Blood Genome-Wide Expression Profiling Studies in Pulmonary Arterial Hypertension
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The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905).
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Revealing the target of PASMC from PAH patients and mechanism
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The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905).
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Altered immune phenotype in peripheral blood cells of patients with scleroderma-associated pulmonary hypertension
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For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21.
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f2132e96ae6c7a4e
required_operations array · 3 items
[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21.
order_basis
analysis_only
id
assay:1
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35710932", "kind": "science-record", "revision": 5, "content_hash": "sha256:9b0ad601f69dcccc6826718962bed6c6d81c82f9d09912a754d9a4aa0ba98fa1", "created_at": "2026-11-01T18:14:41Z", "updated_at": "2026-11-01T22:49:18Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrated bioinformatics analysis reveals marker genes and immune infiltration for pulmonary arterial hypertension.", "doi": "10.1038/s41598-022-14307-6", "pmid": "35710932", "authors": ["Shengxin Tang", "Yue Liu", "Bin Liu"], "journal": "Scientific reports", "year": 2022, "abstract": "Pulmonary arterial hypertension (PAH) is a chronic cardiopulmonary syndrome with high pulmonary vascular load and eventually causing RV heart failure even death. However, the mechanism of pulmonary hypertension remains unclear. The purpose of this research is to detect the underlying key genes and potential mechanism of PAH using several bioinformatic methods. The microarrays GSE22356, GSE131793 and GSE168905 were acquired from the GEO. Subsequently, a host of bioinformatics techniques such as DAVID, STRING, R language and Cytoscape were utilized to investigate DEGs between PAH and healthy controls and conduct GO annotation, KEGG enrichment analysis and PPI network construction etc. Additionally, we predicted the transcription factors regulating DEGs through iRegulon plugin of Cytoscape and CIBERSORT was used to conduct immune infiltration analysis. One thousand two hundred and seventy-seven DEGs (403 up-regulated and 874 down-regulated) were identified from peripheral blood samples of 32 PAH patients and 29 controls, among which SLC4A1, AHSP, ALAS2, CA1, HBD, SNCA, HBM, SELENBP1, SERPINE1 and ITGA2B were detected as hub genes. The functional enrichment changes of DEGs were mainly enriched in protein binding, extracellular exosome, extracellular space, extracellular region and integral component of plasma membrane. The hub genes are chiefly enriched at extracellular exosome, hemoglobin complex, blood microparticle, oxygen transporter activity. Among TF-DEGs network, 42 target DEGs and 6 TFs were predicted with an NES > 4 (TEAD4, TGIF2LY, GATA5, GATA1, GATA2, FOS). Immune infiltration analysis showed that monocytes occupied the largest proportion of immune cells. The trend analysis results of infiltration immune cells illustrated that PAH patients had higher infiltration of NK cell activation, monocyte, T cell CD4 memory activation, and mast cell than healthy controls and lower infiltration of T cell CD4 naive. We detected SLC4A1, AHSP, ALAS2, CA1, HBD, SNCA, HBM, SELENBP1, SERPINE1 and ITGA2B as the most significant markers of PAH. The PAH patients had higher infiltration of NK cell activation, monocyte, T cell CD4 memory activation, and mast cell than healthy controls and lower infiltration of T cell CD4 naive. These identified genes and these immune cells probably have precise regulatory relationships in the development of PAH.", "claims": [{"id": "claim-method", "statement": "For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35710932", "locator": "sections[12] \"Identification of DEGs\" paragraph 2", "quote": "For the purpose of identifying the significant DEGs between the PAH and the healthy group, Limma (linear models for microarray data) package was adopted processing three datasets with |log2 fold change (FC)|≥ 1 and adjusted p value < 0.05 as the thresholds21."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35710932", "locator": "sections[21] \"Data availability\" paragraph 2", "quote": "The gene expression profiles of GSE22356, GSE131793 and GSE168905 were downloaded from Gene Expression Omnibus (GEO) (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE22356, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE131793 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE168905)."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35710932", "locator": "sections[3] \"Identification of DEGs in PAH\" paragraph 2", "quote": "Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Then, we merged up- regulated and down-regulated DEGs in the three datasets, which revealed a total of 403 up-regulated DEGs and 874 down-regulated DEGs in the microarrays.", "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:35710932"], "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:GSE131793"], "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:GSE131793"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35710932", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1038/s41598-022-14307-6", "sha256": 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