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Updated: Apr 18, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
MicroRNA miR-125a-3p modulates molecular pathway of motility and migration in prostate cancer cells
Lihi Ninio-Many1,2, Hadas Grossman1, Mattan Levi1
1Department of Cell and Developmental Biology, Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Abstract:
Fyn kinase is implicated in prostate cancer. We illustrate the role of miR-125a-3p in cellular pathways accounted for motility and migration of prostate cancer cells, probably through its regulation on Fyn expression and Fyn-downstream proteins. Prostate cancer PC3 cells were transiently transfected with empty miR-Vec (control) or with miR-125a-3p. Overexpression of miR-125a-3p reduced migration of PC3 cells and increased apoptosis. Live cell confocal imaging indicated that overexpression of miR-125a-3p reduced the cells' track speed and length and impaired phenotype. Fyn, FAK and paxillin, displayed reduced activity following miR-125a-3p overexpression. Accordingly, actin rearrangement and cells' protrusion formation were impaired. An inverse correlation between miR-125a-3p and Gleason score was observed in human prostate cancer tissues. Our study demonstrated that miR-125a-3p may regulate migration of prostate cancer cells.
Insights
MicroRNA-125a-3p suppresses prostate cancer cell migration and invasion by targeting Fyn kinase. This microRNA may serve as a therapeutic target for reducing prostate cancer progression.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Fyn kinase plays a role in prostate cancer progression.
- MicroRNAs regulate gene expression and are involved in cancer development.
Purpose of the Study:
- To investigate the role of miR-125a-3p in prostate cancer cell motility and migration.
- To determine if miR-125a-3p regulates Fyn kinase expression and downstream signaling pathways.
Main Methods:
- Prostate cancer PC3 cells were transfected with miR-125a-3p mimics or control vectors.
- Cell migration, apoptosis, and live cell imaging were assessed.
- Expression and activity of Fyn, FAK, and paxillin were analyzed.
- Correlation with Gleason score in patient tissues was examined.
Main Results:
- Overexpression of miR-125a-3p reduced PC3 cell migration and increased apoptosis.
- Live cell imaging showed decreased cell track speed, length, and impaired phenotype.
- miR-125a-3p overexpression led to reduced activity of Fyn, FAK, and paxillin.
- Actin rearrangement and cell protrusion formation were impaired.
- An inverse correlation between miR-125a-3p and Gleason score was observed in patient tissues.
Conclusions:
- miR-125a-3p inhibits prostate cancer cell migration and invasion, potentially by regulating Fyn kinase.
- miR-125a-3p may serve as a prognostic biomarker and therapeutic target for prostate cancer.
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