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pmid:31275959

Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer.

Li Li · Haiyan Gu · Lingying Chen · Ping Zhu · Li Zhao · Yuzhuo Wang · Xiang Zhao · Xingguo Zhang · Yonghu Zhang · Peng Shu

BioMed research international · 2019 doi:10.1155/2019/1056431

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Experiment

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Data

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer.
doi
10.1155/2019/1056431
pmid
31275959
authors array · 10 items
[0]
Li Li
[1]
Haiyan Gu
[2]
Lingying Chen
[3]
Ping Zhu
[4]
Li Zhao
[5]
Yuzhuo Wang
[6]
Xiang Zhao
[7]
Xingguo Zhang
[8]
Yonghu Zhang
[9]
Peng Shu
journal
BioMed research international
year
2019
abstract
BACKGROUND: Epithelial ovarian cancer (EOC) is a heterogeneous disease, which has been recently classified into four molecular subtypes, of which the mesenchymal subtype exhibited the worst prognosis. We aimed to identify a microRNA- (miRNA-) based signature by incorporating the molecular modalities involved in the mesenchymal subtype for risk stratification, which would allow the identification of patients who might benefit from more rigorous treatments. METHOD: We characterized the regulatory mechanisms underlying the mesenchymal subtype using network analyses integrating gene and miRNA expression profiles from The Cancer Genome Atlas (TCGA) cohort to identify a miRNA signature for prognosis prediction. RESULTS: We identified four miRNAs as the master regulators of the mesenchymal subtype and developed a risk score model. The 4-miRNA signature significantly predicted overall survival (OS) and progression-free survival (PFS) in discovery (p=0.004 and p=0.04) and two independent public datasets (GSE73582: OS, HR: 2.26 (1.26-4.05), p=0.005, PFS, HR: 2.03 (1.34-3.09), p<0.001; GSE25204: OS, HR: 3.07 (1.73-5.46), p<0.001, PFS, HR: 2.59 (1.72-3.88), p<0.001). Moreover, in multivariate analyses, the miRNA signature maintained as an independent prognostic predictor and achieved superior efficiency compared to the currently used clinical factors. CONCLUSIONS: In conclusion, our network analysis identified a 4-miRNA signature which has prognostic value superior to currently reported clinical covariates. This signature warrants further testing and validation for use in clinical practice.
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To examine the association of the 4-miRNA signature with response to first-line platinum-based therapy [26], we analyzed the chemotherapy response within different risk groups in the GSE25204 cohort and identified an association between the 4-miRNA signature and chemotherapy response (p<0.001, Fisher's exact test; Figure 4).
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sections[12] "3.4. An Association between the 4-miRNA Signature and Chemotherapy Response" paragraph 2
quote
To examine the association of the 4-miRNA signature with response to first-line platinum-based therapy [26], we analyzed the chemotherapy response within different risk groups in the GSE25204 cohort and identified an association between the 4-miRNA signature and chemotherapy response (p<0.001, Fisher's exact test; Figure 4).
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sections[17] "Data Availability" paragraph 2
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The data used to support the findings of this study are available from the corresponding author upon request.
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microRNA alterations associated to clinical response in advanced stage ovarian cancer patients
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3.3. Validation of the 4-miRNA Signature
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To examine the association of the 4-miRNA signature with response to first-line platinum-based therapy [26], we analyzed the chemotherapy response within different risk groups in the GSE25204 cohort and identified an association between the 4-miRNA signature and chemotherapy response (p<0.001, Fisher's exact test; Figure 4).
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To examine the association of the 4-miRNA signature with response to first-line platinum-based therapy [26], we analyzed the chemotherapy response within different risk groups in the GSE25204 cohort and identified an association between the 4-miRNA signature and chemotherapy response (p<0.001, Fisher's exact test; Figure 4).
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31275959", "kind": "science-record", "revision": 8, "content_hash": "sha256:ed93dd85d5566c3febb8bea1a48287a59e75d27a0788330e26334a82c4337132", "created_at": "2026-11-01T15:40:47Z", "updated_at": "2026-11-01T22:44:03Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer.", "doi": "10.1155/2019/1056431", "pmid": "31275959", "authors": ["Li Li", "Haiyan Gu", "Lingying Chen", "Ping Zhu", "Li Zhao", "Yuzhuo Wang", "Xiang Zhao", "Xingguo Zhang", "Yonghu Zhang", "Peng Shu"], "journal": "BioMed research international", "year": 2019, "abstract": "BACKGROUND: Epithelial ovarian cancer (EOC) is a heterogeneous disease, which has been recently classified into four molecular subtypes, of which the mesenchymal subtype exhibited the worst prognosis. We aimed to identify a microRNA- (miRNA-) based signature by incorporating the molecular modalities involved in the mesenchymal subtype for risk stratification, which would allow the identification of patients who might benefit from more rigorous treatments.\nMETHOD: We characterized the regulatory mechanisms underlying the mesenchymal subtype using network analyses integrating gene and miRNA expression profiles from The Cancer Genome Atlas (TCGA) cohort to identify a miRNA signature for prognosis prediction.\nRESULTS: We identified four miRNAs as the master regulators of the mesenchymal subtype and developed a risk score model. The 4-miRNA signature significantly predicted overall survival (OS) and progression-free survival (PFS) in discovery (p=0.004 and p=0.04) and two independent public datasets (GSE73582: OS, HR: 2.26 (1.26-4.05), p=0.005, PFS, HR: 2.03 (1.34-3.09), p<0.001; GSE25204: OS, HR: 3.07 (1.73-5.46), p<0.001, PFS, HR: 2.59 (1.72-3.88), p<0.001). Moreover, in multivariate analyses, the miRNA signature maintained as an independent prognostic predictor and achieved superior efficiency compared to the currently used clinical factors.\nCONCLUSIONS: In conclusion, our network analysis identified a 4-miRNA signature which has prognostic value superior to currently reported clinical covariates. This signature warrants further testing and validation for use in clinical practice.", "claims": [{"id": "claim-method", "statement": "To examine the association of the 4-miRNA signature with response to first-line platinum-based therapy [26], we analyzed the chemotherapy response within different risk groups in the GSE25204 cohort and identified an association between the 4-miRNA signature and chemotherapy response (p<0.001, Fisher's exact test; Figure 4).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:31275959", "locator": "sections[12] \"3.4. 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