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pmid:35810383

Construction of miRNA-lncRNA-mRNA co-expression network affecting EMT-mediated cisplatin resistance in ovarian cancer.

Amirhosein Naghsh-Nilchi · Laleh Ebrahimi Ghahnavieh · Fariba Dehghanian

Journal of cellular and molecular medicine · 2022 doi:10.1111/jcmm.17477

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:35810383
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science-record
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2026-11-01T18:14:51Z
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paper object · 10 fields
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title
Construction of miRNA-lncRNA-mRNA co-expression network affecting EMT-mediated cisplatin resistance in ovarian cancer.
doi
10.1111/jcmm.17477
pmid
35810383
authors array · 3 items
[0]
Amirhosein Naghsh-Nilchi
[1]
Laleh Ebrahimi Ghahnavieh
[2]
Fariba Dehghanian
journal
Journal of cellular and molecular medicine
year
2022
abstract
Platinum resistance is one of the major concerns in ovarian cancer treatment. Recent evidence shows the critical role of epithelial-mesenchymal transition (EMT) in this resistance. Epithelial-like ovarian cancer cells show decreased sensitivity to cisplatin after cisplatin treatment. Our study prospected the association between epithelial phenotype and response to cisplatin in ovarian cancer. Microarray dataset GSE47856 was acquired from the GEO database. After identifying differentially expressed genes (DEGs) between epithelial-like and mesenchymal-like cells, the module identification analysis was performed using weighted gene co-expression network analysis (WGCNA). The gene ontology (GO) and pathway analyses of the most considerable modules were performed. The protein-protein interaction network was also constructed. The hub genes were specified using Cytoscape plugins MCODE and cytoHubba, followed by the survival analysis and data validation. Finally, the co-expression of miRNA-lncRNA-TF with the hub genes was reconstructed. The co-expression network analysis suggests 20 modules relating to the Epithelial phenotype. The antiquewhite4, brown and darkmagenta modules are the most significant non-preserved modules in the Epithelial phenotype and contain the most differentially expressed genes. GO, and KEGG pathway enrichment analyses on these modules divulge that these genes were primarily enriched in the focal adhesion, DNA replication pathways and stress response processes. ROC curve and overall survival rate analysis show that the co-expression pattern of the brown module's hub genes could be a potential prognostic biomarker for ovarian cancer cisplatin resistance.
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After identifying differentially expressed genes (DEGs) between epithelial‐like and mesenchymal‐like cells, the module identification analysis was performed using weighted gene co‐expression network analysis (WGCNA).
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After identifying differentially expressed genes (DEGs) between epithelial‐like and mesenchymal‐like cells, the module identification analysis was performed using weighted gene co‐expression network analysis (WGCNA).
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The data that support the findings of this study are openly available in the NCBI Gene Expression Omnibus (GEO) at (https://www.ncbi.nlm.nih.gov/geo/), reference number (GSE47856, GSE149146).
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sections[28] "DATA AVAILABILITY STATEMENT" paragraph 2
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The data that support the findings of this study are openly available in the NCBI Gene Expression Omnibus (GEO) at (https://www.ncbi.nlm.nih.gov/geo/), reference number (GSE47856, GSE149146).
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ROC curve and overall survival rate analysis show that the co‐expression pattern of the brown module's hub genes could be a potential prognostic biomarker for ovarian cancer cisplatin resistance.
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ROC curve and overall survival rate analysis show that the co‐expression pattern of the brown module's hub genes could be a potential prognostic biomarker for ovarian cancer cisplatin resistance.
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ROC curve and overall survival rate analysis show that the co‐expression pattern of the brown module's hub genes could be a potential prognostic biomarker for ovarian cancer cisplatin resistance.
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Genomic analysis of chromatin conformation and DNA damage distribution in ovarian cancer cell lines derived following acquired resistance to chemotherapy [RNA-Seq]
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Expression data from cultured human ovarian carcinoma cell lines with and without Cisplatin treatment
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After identifying differentially expressed genes (DEGs) between epithelial‐like and mesenchymal‐like cells, the module identification analysis was performed using weighted gene co‐expression network analysis (WGCNA).
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and response to cisplatin in ovarian cancer. Microarray dataset GSE47856 was acquired from the GEO d
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id
assay:1
[1] object · 11 fields
role
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definition_version
f2132e96ae6c7a4e
required_operations array · 3 items
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centrality_scores
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pathway_enrich
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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order_basis
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id
assay:2
Complete file
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Epithelial-like ovarian cancer cells show decreased sensitivity to cisplatin after cisplatin treatment. Our study prospected the association between epithelial phenotype and response to cisplatin in ovarian cancer. Microarray dataset GSE47856 was acquired from the GEO database. After identifying differentially expressed genes (DEGs) between epithelial-like and mesenchymal-like cells, the module identification analysis was performed using weighted gene co-expression network analysis (WGCNA). The gene ontology (GO) and pathway analyses of the most considerable modules were performed. The protein-protein interaction network was also constructed. The hub genes were specified using Cytoscape plugins MCODE and cytoHubba, followed by the survival analysis and data validation. Finally, the co-expression of miRNA-lncRNA-TF with the hub genes was reconstructed. The co-expression network analysis suggests 20 modules relating to the Epithelial phenotype. 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