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pmid:33102593

Screening and Functional Prediction of Key Candidate Genes in Hepatitis B Virus-Associated Hepatocellular Carcinoma.

Xia Chen · Ling Liao · Yuwei Li · Hengliu Huang · Qing Huang · Shaoli Deng

BioMed research international · 2020 doi:10.1155/2020/7653506

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:33102593
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science-record
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2026-11-01T15:41:14Z
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paper object · 10 fields
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title
Screening and Functional Prediction of Key Candidate Genes in Hepatitis B Virus-Associated Hepatocellular Carcinoma.
doi
10.1155/2020/7653506
pmid
33102593
authors array · 6 items
[0]
Xia Chen
[1]
Ling Liao
[2]
Yuwei Li
[3]
Hengliu Huang
[4]
Qing Huang
[5]
Shaoli Deng
journal
BioMed research international
year
2020
abstract
BACKGROUND: The molecular mechanism by which hepatitis B virus (HBV) induces hepatocellular carcinoma (HCC) is still unknown. The genomic expression profile and bioinformatics methods were used to investigate the potential pathogenesis and therapeutic targets for HBV-associated HCC (HBV-HCC). METHODS: The microarray dataset GSE55092 was downloaded from the Gene Expression Omnibus (GEO) database. The data was analyzed by the bioinformatics software to find differentially expressed genes (DEGs). Gene Ontology (GO) enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, ingenuity pathway analysis (IPA), and protein-protein interaction (PPI) network analysis were then performed on DEGs. The hub genes were identified using Centiscape2.2 and Molecular Complex Detection (MCODE) in the Cytoscape software (Cytoscape_v3.7.2). The survival data of these hub genes was downloaded from the Gene Expression Profiling Interactive Analysis (GEPIA). RESULTS: A total of 2264 mRNA transcripts were differentially expressed, including 764 upregulated and 1500 downregulated in tumor tissues. GO analysis revealed that these DEGs were related to the small-molecule metabolic process, xenobiotic metabolic process, and cellular nitrogen compound metabolic process. KEGG pathway analysis revealed that metabolic pathways, complement and coagulation cascades, and chemical carcinogenesis were involved. Diseases and biofunctions showed that DEGs were mainly associated with the following diseases or biological function abnormalities: cancer, organismal injury and abnormalities, gastrointestinal disease, and hepatic system disease. The top 10 upstream regulators were predicted to be activated or inhibited by Z-score and identified 25 networks. The 10 genes with the highest degree of connectivity were defined as the hub genes. Cox regression revealed that all the 10 genes (CDC20, BUB1B, KIF11, TTK, EZH2, ZWINT, NDC80, TPX2, MELK, and KIF20A) were related to the overall survival. CONCLUSION: Our study provided a registry of genes that play important roles in regulating the development of HBV-HCC, assisting us in understanding the molecular mechanisms that underlie the carcinogenesis and progression of HCC.
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title
Viral Expression and Molecular Profiling in Liver Tissue versus Microdissected Hepatocytes in Hepatitis B Virus - Associated Hepatocellular Carcinoma
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Baseline characteristics of the patients with HBV-associated HCC.
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3.1. Differentially Expressed mRNAs in HBV-HCC
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Baseline characteristics of the patients with HBV-associated HCC.
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[1]
10 : 1
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0.88 ± 0.47
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36.18 ± 17.8
[6] array · 2 items
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[1]
39.09 ± 17.0
[7] array · 2 items
[0]
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93.9 ± 83.56
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[0]
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[1]
[9] array · 2 items
[0]
G2 (%)
[1]
64
[10] array · 2 items
[0]
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[1]
27
[11] array · 2 items
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[1]
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[12] array · 2 items
[0]
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[1]
100
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[1]
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[0]
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[1]
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[15] array · 2 items
[0]
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[1]
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Top 10 upstream regulators that are predicted to be activated by Z-score.
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3.4. Upstream Regulator Analysis
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Table 2
caption
Top 10 upstream regulators that are predicted to be activated by Z-score.
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Upstream regulator
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Molecule type
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SB203580
[1]
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Top 10 upstream regulators that are predicted to be inhibited by Z-score.
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PMC7568806
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13
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3.4. Upstream Regulator Analysis
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Table 3
caption
Top 10 upstream regulators that are predicted to be inhibited by Z-score.
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The degree values of top 10 hub genes.
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15
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3.6. Key Candidate Gene Identification with DEG PPI Network
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Table 4
caption
The degree values of top 10 hub genes.
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[0] array · 4 items
[0]
Gene symbol
[1]
Gene description
[2]
Fold change
[3]
Degree
[1] array · 4 items
[0]
CDC20
[1]
Cell division cycle 20
[2]
4.16
[3]
36
[2] array · 4 items
[0]
BUB1B
[1]
BUB1 mitotic checkpoint serine
[2]
6.17
[3]
30
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[0]
KIF11
[1]
Kinesin family member 11
[2]
3.66
[3]
29
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[0]
TTK
[1]
TTK protein kinase
[2]
5.02
[3]
28
[5] array · 4 items
[0]
EZH2
[1]
Enhancer of zeste homolog 2
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3.24
[3]
28
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[0]
ZWINT
[1]
ZW10 interacting kinetochore protein
[2]
3.55
[3]
27
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[0]
NDC80
[1]
NDC80 kinetochore complex component
[2]
7.72
[3]
27
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[0]
TPX2
[1]
Microtubule nucleation factor
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2.31
[3]
27
[9] array · 4 items
[0]
MELK
[1]
Maternal embryonic leucine zipper kinase
[2]
7.15
[3]
27
[10] array · 4 items
[0]
KIF20A
[1]
Kinesin family member 20A
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5.58
[3]
26
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[0]
asset:data:geo:GSE55092 not downloaded
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asset:data:geo:GSE55092 licence not read
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r HBV-associated HCC (HBV-HCC). METHODS: The microarray dataset GSE55092 was downloaded from the Gen
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33102593", "kind": "science-record", "revision": 7, "content_hash": "sha256:bedf1d8f80c93d8953856ed19d6d83893dc67f76eeab28c6d7c38f5100108257", "created_at": "2026-11-01T15:41:14Z", "updated_at": "2026-11-01T22:02:23Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Screening and Functional Prediction of Key Candidate Genes in Hepatitis B Virus-Associated Hepatocellular Carcinoma.", "doi": "10.1155/2020/7653506", "pmid": "33102593", "authors": ["Xia Chen", "Ling Liao", "Yuwei Li", "Hengliu Huang", "Qing Huang", "Shaoli Deng"], "journal": "BioMed research international", "year": 2020, "abstract": "BACKGROUND: The molecular mechanism by which hepatitis B virus (HBV) induces hepatocellular carcinoma (HCC) is still unknown. The genomic expression profile and bioinformatics methods were used to investigate the potential pathogenesis and therapeutic targets for HBV-associated HCC (HBV-HCC).\nMETHODS: The microarray dataset GSE55092 was downloaded from the Gene Expression Omnibus (GEO) database. The data was analyzed by the bioinformatics software to find differentially expressed genes (DEGs). Gene Ontology (GO) enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, ingenuity pathway analysis (IPA), and protein-protein interaction (PPI) network analysis were then performed on DEGs. The hub genes were identified using Centiscape2.2 and Molecular Complex Detection (MCODE) in the Cytoscape software (Cytoscape_v3.7.2). The survival data of these hub genes was downloaded from the Gene Expression Profiling Interactive Analysis (GEPIA).\nRESULTS: A total of 2264 mRNA transcripts were differentially expressed, including 764 upregulated and 1500 downregulated in tumor tissues. GO analysis revealed that these DEGs were related to the small-molecule metabolic process, xenobiotic metabolic process, and cellular nitrogen compound metabolic process. KEGG pathway analysis revealed that metabolic pathways, complement and coagulation cascades, and chemical carcinogenesis were involved. Diseases and biofunctions showed that DEGs were mainly associated with the following diseases or biological function abnormalities: cancer, organismal injury and abnormalities, gastrointestinal disease, and hepatic system disease. The top 10 upstream regulators were predicted to be activated or inhibited by Z-score and identified 25 networks. The 10 genes with the highest degree of connectivity were defined as the hub genes. Cox regression revealed that all the 10 genes (CDC20, BUB1B, KIF11, TTK, EZH2, ZWINT, NDC80, TPX2, MELK, and KIF20A) were related to the overall survival.\nCONCLUSION: Our study provided a registry of genes that play important roles in regulating the development of HBV-HCC, assisting us in understanding the molecular mechanisms that underlie the carcinogenesis and progression of HCC.", "claims": [{"id": "claim-data-access", "statement": "The data used to support the findings of this study are available from the corresponding author upon reasonable request.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:33102593", "locator": "sections[20] \"Data Availability\" paragraph 2", "quote": "The data used to support the findings of this study are available from the corresponding author upon reasonable request."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "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:33102593"], "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:GSE55092"], "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:GSE55092"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:33102593", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1155/2020/7653506", "sha256": "sha256:fac3257dd980218cc90491b72626fd600bdeee046eb17523be597e8c00a26e39", "bytes": 35418, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1155/2020/7653506", "version": null, "note": "Full article fetched from PMC; 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