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Published on: August 2, 2024
MiR-193a-5p serves as an inhibitor in ovarian cancer cells through RAB11A
Yazhuo Wang1, Na Li2, Jing Zhao1
1Department of Gynecology, Hebei General Hospital, China.
Abstract:
Ovarian cancer is often not diagnosed until it is in advanced stages and its cure rate is relatively low. Thus, this investigation is concerned about the pathogenesis of this cancer. Differential expression analysis was undertaken on messenger RNA (mRNA) and microRNA (miRNA) data of ovarian cancer in Gene Expression Profiling Interactive Analysis and Gene Expression Omnibus databases. RAB11A mRNA and miR-193a-5p expression levels were tested by quantitative polymerase chain reaction. The targeting relationship between RAB11A and miR-193a-5p was verified by dual-luciferase assay. Cell behaviors of ovarian cancer were tested by Cell-Counting-Kit-8, colony formation and transwell assays. Expression of RAB11A protein and the proteins associated with Wnt/β-catenin was tested by western blot. RAB11A high expression and miR-193a-5p low expression were found in ovarian cancer cells. RAB11A was targeted by miR-193a-5p. Cellular function experiments proved that RAB11A facilitated Wnt/β-catenin signaling activation and deteriorated ovarian cancer progression. Rescue experiments exhibited two results: miR-193a-5p hindered proliferation, migration and invasion of ovarian cancer cells, and this suppression was counteracted by overexpression of RAB11A and miR-193a-5p. Furthermore, miR-193a-5p repressed RAB11A-mediated Wnt/β-catenin activation. Altogether, miR-193a-5p served as a modulator in ovarian cancer cells via targeting RAB11A.
Insights
MicroRNA-193a-5p targets RAB11A, inhibiting ovarian cancer progression. This microRNA (miRNA) suppresses proliferation and invasion by repressing Wnt/β-catenin signaling, offering a potential therapeutic target for ovarian cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Ovarian cancer diagnosis is often delayed, leading to low cure rates.
- Understanding the pathogenesis of ovarian cancer is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of RAB11A messenger RNA (mRNA) and microRNA (miRNA) in ovarian cancer pathogenesis.
- To elucidate the regulatory relationship between RAB11A and miR-193a-5p and their impact on ovarian cancer progression.
Main Methods:
- Differential expression analysis of mRNA and miRNA data from public databases (GEPIA, GEO).
- Quantitative polymerase chain reaction (qPCR) to measure RAB11A and miR-193a-5p levels.
- Dual-luciferase assay to confirm targeting relationship.
- Cellular assays (CCK-8, colony formation, Transwell) to assess cell behaviors.
- Western blot to analyze protein expression (RAB11A, Wnt/β-catenin pathway proteins).
Main Results:
- RAB11A mRNA was highly expressed, while miR-193a-5p was lowly expressed in ovarian cancer cells.
- miR-193a-5p directly targets RAB11A.
- RAB11A promotes ovarian cancer progression by activating Wnt/β-catenin signaling.
- miR-193a-5p inhibits ovarian cancer cell proliferation, migration, and invasion.
- Overexpression of RAB11A counteracted the suppressive effects of miR-193a-5p.
Conclusions:
- miR-193a-5p acts as a tumor suppressor in ovarian cancer by targeting RAB11A.
- The miR-193a-5p/RAB11A axis modulates Wnt/β-catenin signaling, impacting ovarian cancer progression.
- Targeting the miR-193a-5p/RAB11A pathway may offer a novel therapeutic strategy for ovarian cancer.
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