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Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
Identification of lncRNA-miRNA-mRNA regulatory network associated with epithelial ovarian cancer cisplatin-resistant
Xin Zhao1, Dong-Yang Tang2, Xu Zuo1
1Department of Pharmacy, Xinxiang Central Hospital, Xinxiang, Henan, P. R. China.
Abstract:
To construct a long noncoding RNA (lncRNA)-microRNA (miRNA)-messenger RNA (mRNA) regulatory network related to epithelial ovarian cancer (EOC) cisplatin-resistant, differentially expressed genes (DEGs), differentially expressed lncRNAs (DELs), and differentially expressed miRNAs (DEMs) between MDAH and TOV-112D cells lines were identified. Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were conducted to analyze the biological functions of DEGs. Downstream mRNAs or upstream lncRNAs for miRNAs were analyzed at miRTarBase 7.0 or DIANA-LncBase V2, respectively. A total of 485 significant DEGs, 85 DELs, and 5 DEMs were identified. Protein-protein interaction (PPI) network of DEGs contrains 81 nodes and 141 edges was constructed, and 25 hub genes related to EOC cisplatin-resistant were identified. Subsequently, a lncRNA-miRNA-mRNA regulatory network contains 4 lncRNAs, 4 miRNAs, and 35 mRNAs was established. Taken together, our study provided evidence concerning the alteration genes involved in EOC cisplatin-resistant, which will help to unravel the mechanisms underlying drug resistant.
Insights
This study identifies key genes and regulatory networks involved in cisplatin resistance in epithelial ovarian cancer (EOC). The findings offer insights into the molecular mechanisms driving drug resistance in EOC.
Area of Science:
- Genomics
- Molecular Biology
- Oncology
Background:
- Epithelial ovarian cancer (EOC) often develops resistance to cisplatin chemotherapy.
- Understanding the molecular mechanisms of cisplatin resistance is crucial for improving treatment outcomes.
Purpose of the Study:
- To construct a long noncoding RNA (lncRNA)-microRNA (miRNA)-messenger RNA (mRNA) regulatory network associated with cisplatin resistance in EOC.
- To identify differentially expressed genes (DEGs), lncRNAs (DELs), and miRNAs (DEMs) in cisplatin-resistant EOC cells.
Main Methods:
- Differential gene, lncRNA, and miRNA expression analysis between cisplatin-resistant and sensitive cell lines.
- Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.
- Construction of protein-protein interaction (PPI) networks and lncRNA-miRNA-mRNA regulatory networks using databases like miRTarBase and DIANA-LncBase.
Main Results:
- Identified 485 significant DEGs, 85 DELs, and 5 DEMs.
- Constructed a PPI network revealing 25 hub genes critical for cisplatin resistance.
- Established a lncRNA-miRNA-mRNA regulatory network comprising 4 lncRNAs, 4 miRNAs, and 35 mRNAs.
Conclusions:
- The study elucidates crucial gene alterations and regulatory networks implicated in EOC cisplatin resistance.
- These findings contribute to understanding the molecular basis of drug resistance and may guide future therapeutic strategies.
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