Why the study?
Epithelial ovarian cancer causes high morbidity and mortality, and investigating the underlying mechanism between lncRNA and epithelial ovarian cancer is important.
LINC01503 is identified as a potential diagnostic and prognostic biomarker and oncogene in epithelial ovarian cancer.
LINC01503 merits exploration as an EOC biomarker and target; animal data leave open clinical translation pending human studies.
Background: Epithelial ovarian cancer (EOC) is a disease with high morbidity and mortality worldwide, which is seriously harmful to female health. LncRNA has an important relationship with the occurrence and development of tumors. Hence, the investigation of the underlying mechanism between LncRNA and EOC is of great importance. Results: In this study, we found that LINC01503 was highly expressed in EOC with a poor prognosis based on microarray datasets GSE119056 and GSE135886 obtained from Gene Expression Omnibus (GEO) database, and this result was verified by RT-qPCR. The database lncBase Predicted v.2 and starBase v2.0 were used to predict the targeted relationship of lncRNA-miRNA-mRNA, then the ceRNA network was established by Cytoscape software. Following, the expression and overall survival (OS) analysis of key lncRNAs were analyzed by GEPIA and Kaplan-Meier plotter database. Gene Ontology (GO) functional enrichment analysis was performed by DAVID database and enriched two cancer related biological processes (BP) that response to endoplasmic reticulum stress and IRE1-mediated unfolded protein. Moreover, we verified that LINC01503 was an oncogene regulated by C-terminal binding protein 1 (CTBP1) to promote cell proliferation, migration and inhibited cell apoptosis in ovarian cancer. Conclusion: In conclusion, these results identified LINC01503 as a potential gene for EOC diagnosis and prognosis.
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Wang et al. (2021) studied this question.
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