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pmid:35223598

Identification of Hub Genes in Pancreatic Ductal Adenocarcinoma Using Bioinformatics Analysis.

Congcong Wang · Jianping Guo · Xiaoyang Zhao · Jia Jia · Wenting Xu · Peng Wan · Changgang Sun

Iranian journal of public health · 2021 doi:10.18502/ijph.v50i11.7578

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

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:35223598
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science-record
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2026-11-01T17:36:59Z
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2026-11-01T22:48:34Z
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paper object · 10 fields
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title
Identification of Hub Genes in Pancreatic Ductal Adenocarcinoma Using Bioinformatics Analysis.
doi
10.18502/ijph.v50i11.7578
pmid
35223598
authors array · 7 items
[0]
Congcong Wang
[1]
Jianping Guo
[2]
Xiaoyang Zhao
[3]
Jia Jia
[4]
Wenting Xu
[5]
Peng Wan
[6]
Changgang Sun
journal
Iranian journal of public health
year
2021
abstract
BACKGROUND: To address the biomarkers that correlated with the prognosis of patients with PDCA using bioinformatics analysis. METHODS: The raw data of genes were obtained from the Gene Expression Omnibus. We screened differently expressed genes (DEGs) by Rstudio. Database for Annotation, Visualization and Intergrated Discovery was used to investigate their biological function by Gene Ontology(GO) and Kyoto Encyclopedia of Genes (KEGG) analysis. Protein-protein interaction of these DEGs were analyzed based on the Search Tool for the Retrieval of Interacting Genes database (STRING) and visualized by Cytoscape. Genes calculated by Cyto-Hubba with degree >10 were identified as hub genes. Then, the identified hub genes were verified by UALCAN online analysis tool to evaluate the prognostic value in PDCA. RESULTS: Three expression profiles (GSE15471, GSE16515 and GSE32676) were downloaded from GEO database. The three sets of DEGs exhibited an intersection consisting of 223 genes (214 upregulated DEGs and 9 downregulated DEGs). GO analysis showed that the 223 DEGs were significantly enriched in extracellular exosome, plasma membrane and extracellular space. ECM-receptor interaction, PI3K-Akt signaling pathway and Focal adhesion were the most significantly enriched pathway according to KEGG analysis. By combining the results of Cytohubba, 30 hub genes with a high degree of connectivity were picked out. Finally, we candidated 3 biomarkers by UALCAN online survival analysis, including CEP55, ANLN and PRC1. CONCLUSION: we identified CEP55, ANLN and PRC1 may be the potential biomarkers and therapeutic targets of PDCA, which used for prognostic assessment and scheme selection.
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The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues.
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sections[5] "Identification of DEGs" paragraph 2
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The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues.
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The study identified 223 common PDCA-related DEGs and nominated CEP55, ANLN and PRC1 as potential prognostic biomarkers and therapeutic targets.
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The three sets of DEGs exhibited an intersection consisting of 223 genes (214 upregulated DEGs and 9 downregulated DEGs).
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sections[0] "Abstract" paragraph 3
quote
Finally, we candidated 3 biomarkers by UALCAN online survival analysis, including CEP55, ANLN and PRC1.
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sections[0] "Abstract" paragraph 4
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we identified CEP55, ANLN and PRC1 may be the potential biomarkers and therapeutic targets of PDCA, which used for prognostic assessment and scheme selection.
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The study identified 223 common PDCA-related DEGs and nominated CEP55, ANLN and PRC1 as potential prognostic biomarkers and therapeutic targets.
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Whole-Tissue Gene Expression Study of Pancreatic Ductal Adenocarcinoma
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The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues.
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[2]
fdr_bh
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues.
order_basis
analysis_only
id
assay:1
Complete file
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We screened differently expressed genes (DEGs) by Rstudio. Database for Annotation, Visualization and Intergrated Discovery was used to investigate their biological function by Gene Ontology(GO) and Kyoto Encyclopedia of Genes (KEGG) analysis. Protein-protein interaction of these DEGs were analyzed based on the Search Tool for the Retrieval of Interacting Genes database (STRING) and visualized by Cytoscape. Genes calculated by Cyto-Hubba with degree >10 were identified as hub genes. Then, the identified hub genes were verified by UALCAN online analysis tool to evaluate the prognostic value in PDCA.\nRESULTS: Three expression profiles (GSE15471, GSE16515 and GSE32676) were downloaded from GEO database. The three sets of DEGs exhibited an intersection consisting of 223 genes (214 upregulated DEGs and 9 downregulated DEGs). GO analysis showed that the 223 DEGs were significantly enriched in extracellular exosome, plasma membrane and extracellular space. ECM-receptor interaction, PI3K-Akt signaling pathway and Focal adhesion were the most significantly enriched pathway according to KEGG analysis. By combining the results of Cytohubba, 30 hub genes with a high degree of connectivity were picked out. Finally, we candidated 3 biomarkers by UALCAN online survival analysis, including CEP55, ANLN and PRC1.\nCONCLUSION: we identified CEP55, ANLN and PRC1 may be the potential biomarkers and therapeutic targets of PDCA, which used for prognostic assessment and scheme selection.", "claims": [{"id": "claim-method", "statement": "The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35223598", "locator": "sections[5] \"Identification of DEGs\" paragraph 2", "quote": "The Limma package in Bioconductor was used to screen DEGs in PDCA tissues compared normal pancreatic tissues."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All of the raw data were freely available online", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35223598", "locator": "sections[3] \"Gene expression data\" paragraph 2", "quote": "All of the raw data were freely available online"}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified 223 common PDCA-related DEGs and nominated CEP55, ANLN and PRC1 as potential prognostic biomarkers and therapeutic targets.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35223598", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "The three sets of DEGs exhibited an intersection consisting of 223 genes (214 upregulated DEGs and 9 downregulated DEGs)."}, {"asset": "source:pmid:35223598", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Finally, we candidated 3 biomarkers by UALCAN online survival analysis, including CEP55, ANLN and PRC1."}, {"asset": "source:pmid:35223598", "locator": "sections[0] \"Abstract\" paragraph 4", "quote": "we identified CEP55, ANLN and PRC1 may be the potential biomarkers and therapeutic targets of PDCA, which used for prognostic assessment and scheme selection."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "The study identified 223 common PDCA-related DEGs and nominated CEP55, ANLN and PRC1 as potential prognostic biomarkers and therapeutic targets.", "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:35223598"], "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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