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pmid:35300136

Discovering Novel Biomarkers Associated with the Pathogenesis of Psoriasis: Evidence from Bioinformatic Analysis.

Yang Yang · Shaoqiong Xie · Wencheng Jiang · Suwei Tang · Yuling Shi

International journal of general medicine · 2022 doi:10.2147/IJGM.S354985

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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pmid:35300136
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title
Discovering Novel Biomarkers Associated with the Pathogenesis of Psoriasis: Evidence from Bioinformatic Analysis.
doi
10.2147/IJGM.S354985
pmid
35300136
authors array · 5 items
[0]
Yang Yang
[1]
Shaoqiong Xie
[2]
Wencheng Jiang
[3]
Suwei Tang
[4]
Yuling Shi
journal
International journal of general medicine
year
2022
abstract
Objective: This study aimed to investigate key biomarkers and their molecular pathogenesis in psoriasis. Methods: Differentially expressed genes (DEGs) of datasets (GSE13355, GSE30999, and GSE106992) obtained from Gene Expression Omnibus (GEO) were identified using Venn diagram. Function and pathway enrichment analyses were performed. Protein-protein interaction (PPI) network and the hub genes were constructed. The correlation between normal tissue and infiltrating immune cells was analyzed by CIBERSORT. ROC analysis was performed to distinguish between skin lesion samples and skin non-lesion samples. Analyze the highest expression of single gene in the whole body within the Human Protein Atlas (HPA) database. Effect of CXCL8 expression level on proliferation, invasion, migration and apoptosis of HaCat cells was detected by qPCR. Results: A total of 239 pairs of normal and lesional skin samples were downloaded. PPI network revealed a tight interaction among 197 DEGs. The GO enrichment analysis showed that these genes were markedly enriched in the "defense response to virus", "type I interferon signaling pathway", and "cell response to type I interferon" categories. The KEGG pathway analysis showed that the DEGs were mainly in the NOD-like receptor axis, interaction between cytokine and cytokine receptor and the IL-17 axis. PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells. 6 miRNAs were predicted to be related to CXCL8. CXCL8 was most widely distributed in lymphoid tissues and plays a role in psoriatic inflammatory lesions by promoting cell proliferation, migration, and anti-apoptosis. Conclusion: CXCL8 plays a key role in psoriasis development. This study provided new insights into the exploration of molecular mechanisms and therapeutic targets of psoriasis.
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DEG analysis was done with R 3.4.1ʹs (https://www.r-project.org/) Affy and Limma package.
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sections[30] "Data Sharing Statement" paragraph 2
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All data generated or analysed during this study are included in this published article.
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PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells.
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PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells.
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PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells.
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Cellular and Molecular Changes in Psoriasis Lesions Induced by Ustekinumab: Distinct Differences in Responders vs. Non-Responders
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sample_count
170
group_sizes
null
group_sizes_basis
null
platform
570
taxon
Homo sapiens
title
Expression data from skin biopsy samples from patients with moderate-to-severe psoriasis
resolution_checked_at
2026-11-01T15:39:54Z
resolution_check
identifier_resolution_only_no_download_no_licence_read
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[0]
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[2]
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[3]
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[4]
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[5]
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specific
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evidence object · 3 fields
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DEG analysis was done with R 3.4.1ʹs (https://www.r-project.org/) Affy and Limma package.
[1] object · 10 fields
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[0]
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evidence object · 3 fields
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state
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[6]
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[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
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readiness object · 8 fields
state
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: limma_voom.
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tier
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capability:computational_analysis
availability_state
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basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
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accessions array · 3 items
[0]
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[1]
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resolved_accessions array · 3 items
[0]
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[1]
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[2]
GSE106992
statements array · 1 item
[0]
All data generated or analysed during this study are included in this published article.
basis
The paper names GSE13355, GSE30999, GSE106992 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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[0]
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reader object · 5 fields
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provider
minimax
provider_family
minimax
read_at
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verbatim
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paper
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type
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GEO GSE106992
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[3]
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[4]
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[5]
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[0]
el on proliferation, invasion, migration and apoptosis of HaCat cells was detected by qPCR. Results
[1]
ting cell proliferation, migration, and anti-apoptosis. Conclusion: CXCL8 plays a key role in psori
order_basis
paper_text_order:864
id
assay:1
[1] object · 11 fields
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99e1195c7d6f
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and apoptosis of HaCat cells was detected by qPCR. Results: A total of 239 pairs of normal and
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Materials and Methods Immunohistochemical (HIC) Analysis of Lymph Nodes Through HPA Da
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DEG analysis was done with R 3.4.1ʹs (https://www.r-project.org/) Affy and Limma package.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35300136", "kind": "science-record", "revision": 5, "content_hash": "sha256:a78a6c6072535365de0e38a0f02c13826f246e5ba145e42d472079adda64172e", "created_at": "2026-11-01T18:14:05Z", "updated_at": "2026-11-01T22:48:41Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Discovering Novel Biomarkers Associated with the Pathogenesis of Psoriasis: Evidence from Bioinformatic Analysis.", "doi": "10.2147/IJGM.S354985", "pmid": "35300136", "authors": ["Yang Yang", "Shaoqiong Xie", "Wencheng Jiang", "Suwei Tang", "Yuling Shi"], "journal": "International journal of general medicine", "year": 2022, "abstract": "Objective: This study aimed to investigate key biomarkers and their molecular pathogenesis in psoriasis.\nMethods: Differentially expressed genes (DEGs) of datasets (GSE13355, GSE30999, and GSE106992) obtained from Gene Expression Omnibus (GEO) were identified using Venn diagram. Function and pathway enrichment analyses were performed. Protein-protein interaction (PPI) network and the hub genes were constructed. The correlation between normal tissue and infiltrating immune cells was analyzed by CIBERSORT. ROC analysis was performed to distinguish between skin lesion samples and skin non-lesion samples. Analyze the highest expression of single gene in the whole body within the Human Protein Atlas (HPA) database. Effect of CXCL8 expression level on proliferation, invasion, migration and apoptosis of HaCat cells was detected by qPCR.\nResults: A total of 239 pairs of normal and lesional skin samples were downloaded. PPI network revealed a tight interaction among 197 DEGs. The GO enrichment analysis showed that these genes were markedly enriched in the \"defense response to virus\", \"type I interferon signaling pathway\", and \"cell response to type I interferon\" categories. The KEGG pathway analysis showed that the DEGs were mainly in the NOD-like receptor axis, interaction between cytokine and cytokine receptor and the IL-17 axis. PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells. 6 miRNAs were predicted to be related to CXCL8. CXCL8 was most widely distributed in lymphoid tissues and plays a role in psoriatic inflammatory lesions by promoting cell proliferation, migration, and anti-apoptosis.\nConclusion: CXCL8 plays a key role in psoriasis development. This study provided new insights into the exploration of molecular mechanisms and therapeutic targets of psoriasis.", "claims": [{"id": "claim-method", "statement": "DEG analysis was done with R 3.4.1ʹs (https://www.r-project.org/) Affy and Limma package.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35300136", "locator": "sections[4] \"Screening of DEGs\" paragraph 2", "quote": "DEG analysis was done with R 3.4.1ʹs (https://www.r-project.org/) Affy and Limma package."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All data generated or analysed during this study are included in this published article.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35300136", "locator": "sections[30] \"Data Sharing Statement\" paragraph 2", "quote": "All data generated or analysed during this study are included in this published article."}], "state": "complete"}, {"id": "claim-target-result", "statement": "PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35300136", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "PPI analysis showed that CXCL8 was the novel hub gene of psoriasis and correlated to 22 types of infiltrating immune cells.", "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:35300136"], "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:GSE106992"], "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:GSE106992"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:35300136", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.2147/IJGM.S354985", "sha256": 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