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

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...

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Autores principales: Li, Li, Gu, Haiyan, Chen, Lingying, Zhu, Ping, Zhao, Li, Wang, Yuzhuo, Zhao, Xiang, Zhang, Xingguo, Zhang, Yonghu, Shu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582839/
https://www.ncbi.nlm.nih.gov/pubmed/31275959
http://dx.doi.org/10.1155/2019/1056431
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author Li, Li
Gu, Haiyan
Chen, Lingying
Zhu, Ping
Zhao, Li
Wang, Yuzhuo
Zhao, Xiang
Zhang, Xingguo
Zhang, Yonghu
Shu, Peng
author_facet Li, Li
Gu, Haiyan
Chen, Lingying
Zhu, Ping
Zhao, Li
Wang, Yuzhuo
Zhao, Xiang
Zhang, Xingguo
Zhang, Yonghu
Shu, Peng
author_sort Li, Li
collection PubMed
description 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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spelling pubmed-65828392019-07-04 Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer Li, Li Gu, Haiyan Chen, Lingying Zhu, Ping Zhao, Li Wang, Yuzhuo Zhao, Xiang Zhang, Xingguo Zhang, Yonghu Shu, Peng Biomed Res Int Research Article 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. Hindawi 2019-06-04 /pmc/articles/PMC6582839/ /pubmed/31275959 http://dx.doi.org/10.1155/2019/1056431 Text en Copyright © 2019 Li Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Li
Gu, Haiyan
Chen, Lingying
Zhu, Ping
Zhao, Li
Wang, Yuzhuo
Zhao, Xiang
Zhang, Xingguo
Zhang, Yonghu
Shu, Peng
Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title_full Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title_fullStr Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title_full_unstemmed Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title_short Integrative Network Analysis Reveals a MicroRNA-Based Signature for Prognosis Prediction of Epithelial Ovarian Cancer
title_sort integrative network analysis reveals a microrna-based signature for prognosis prediction of epithelial ovarian cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582839/
https://www.ncbi.nlm.nih.gov/pubmed/31275959
http://dx.doi.org/10.1155/2019/1056431
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