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pmid:35022380

Comprehensive Analysis of Tripterine Anti-Ovarian Cancer Effects Using Weighted Gene Co-Expression Network Analysis and Molecular Docking.

Xi Long · Leping Liu · Qinyu Zhao · Xinyi Xu · Pingan Liu · Guoming Zhang · Jie Lin

Medical science monitor : international medical journal of experimental and clinical research · 2022 doi:10.12659/MSM.932139

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:35022380
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title
Comprehensive Analysis of Tripterine Anti-Ovarian Cancer Effects Using Weighted Gene Co-Expression Network Analysis and Molecular Docking.
doi
10.12659/MSM.932139
pmid
35022380
authors array · 7 items
[0]
Xi Long
[1]
Leping Liu
[2]
Qinyu Zhao
[3]
Xinyi Xu
[4]
Pingan Liu
[5]
Guoming Zhang
[6]
Jie Lin
journal
Medical science monitor : international medical journal of experimental and clinical research
year
2022
abstract
BACKGROUND Ovarian cancer has the highest mortality of gynecological cancers worldwide. The aim of this study was to identify the role of tripterine against ovarian cancer. MATERIAL AND METHODS GSE18520 and GSE12470 data sets were downloaded from the GEO database. WGCNA was used to analyze gene modules and hub genes related to ovarian cancer. These hub genes were intersected with tripterine targets, and GO and KEGG enrichment analyses were performed. HPA and GEPIA determined the expression of tripterine anti-ovarian hub genes in tumor tissues. Kaplan-Meier plotter was used to explore the role of hub genes in ovarian cancer prognosis. AutoDock was used to conduct molecular docking of tripterine and hub genes to observe whether the combination was stable. RESULTS By differential analysis of gene expression and the construction of WGCNA co-expression network, 5 hub genes, ARHGAP11A, MUC1, HBB, RUNX1T1, and FUT8, were screened by module gene screening. Seven biological processes and 20 KEGG-related pathways were obtained by gene enrichment. The expression of tripterine anti-ovarian hub genes ARHGAP11A, MUC1, and FUT8 were obtained by HPA and GEPIA. Using Kaplan-Meier plotter, the survival of ovarian cancer was negatively correlated with ARHGAP11A, MUC1, and FUT8. Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role. CONCLUSIONS Tripterine may be involved in megakaryocyte development and platelet production through potential genes ARHGAP11A, MUC1, HBB, RUNX1T1, and FUT8 and may have an anti-ovarian cancer effect in immune factors signaling, transporting and exchanging oxygen pathways, and autophagy pathways, through these 5 key genes.
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Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role.
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The aim of this study was to identify the role of tripterine against ovarian cancer. MATERIAL AND METHODS GSE18520 and GSE12470 data sets were downloaded from the GEO database. WGCNA was used to analyze gene modules and hub genes related to ovarian cancer. These hub genes were intersected with tripterine targets, and GO and KEGG enrichment analyses were performed. HPA and GEPIA determined the expression of tripterine anti-ovarian hub genes in tumor tissues. Kaplan-Meier plotter was used to explore the role of hub genes in ovarian cancer prognosis. AutoDock was used to conduct molecular docking of tripterine and hub genes to observe whether the combination was stable. RESULTS By differential analysis of gene expression and the construction of WGCNA co-expression network, 5 hub genes, ARHGAP11A, MUC1, HBB, RUNX1T1, and FUT8, were screened by module gene screening. Seven biological processes and 20 KEGG-related pathways were obtained by gene enrichment. The expression of tripterine anti-ovarian hub genes ARHGAP11A, MUC1, and FUT8 were obtained by HPA and GEPIA. Using Kaplan-Meier plotter, the survival of ovarian cancer was negatively correlated with ARHGAP11A, MUC1, and FUT8. Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role. CONCLUSIONS Tripterine may be involved in megakaryocyte development and platelet production through potential genes ARHGAP11A, MUC1, HBB, RUNX1T1, and FUT8 and may have an anti-ovarian cancer effect in immune factors signaling, transporting and exchanging oxygen pathways, and autophagy pathways, through these 5 key genes.", "claims": [{"id": "claim-method", "statement": "WGCNA was used to analyze gene modules and hub genes related to ovarian cancer.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35022380", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "WGCNA was used to analyze gene modules and hub genes related to ovarian cancer."}], "state": "complete"}, {"id": "claim-data-access", "statement": "GSE18520 and GSE12470 data sets were downloaded from the GEO database.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:35022380", "locator": "sections[0] \"Abstract\" paragraph 2", "quote": "GSE18520 and GSE12470 data sets were downloaded from the GEO database."}], "state": "complete"}, {"id": "claim-target-result", "statement": "Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role.", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:35022380", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "Molecular docking showed the combination of tripterine and FUT8 was most stable, having the greatest potential role.", "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:35022380"], "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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