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An Orthotopic Bladder Cancer Model for Gene Delivery Studies
Published on: December 1, 2013
A miR-124-3p/PKC-δ Regulatory Axis Restrains Bladder Cancer Growth and Malignant Progression
Yu-Cheng Kuo1,2, Hsiao-Yu Wang3, Tsai-Lan Liao4
1School of Medicine, College of Medicine, China Medical University, Taichung, Taiwan, R.O.C.
In Vivo (Athens, Greece)
|June 30, 2026
Summary
MicroRNA-124-3p suppresses bladder cancer progression by targeting Protein Kinase C delta (PKC-δ). This novel axis inhibits cell migration, invasion, and stemness, offering potential therapeutic strategies for bladder cancer.
Area of Science:
- Oncology
- Molecular Biology
- Gene Regulation
Background:
- Bladder cancer exhibits high recurrence and metastasis rates, necessitating new molecular targets.
- Protein kinase C delta (PKC-δ) is implicated in tumor progression, but its regulation in bladder cancer is unclear.
- MicroRNAs (miRNAs) are key regulators; miR-124-3p acts as a tumor suppressor, but its role with PKC-δ in bladder cancer is unestablished.
Purpose of the Study:
- To investigate the regulatory role of the miR-124-3p/PKC-δ axis.
- To determine the impact of this axis on bladder cancer cell malignant phenotypes.
Main Methods:
- Utilized human bladder cancer cell lines (TSGH8301, T24).
- Administered PKC inhibitor rottlerin and transfected with miR-124-3p mimic.
- Assessed cell viability, proliferation, migration, invasion, epithelial-mesenchymal transition (EMT), and stemness via various assays and western blotting.
Main Results:
- PKC inhibition (rottlerin) suppressed proliferation and increased miR-124-3p expression.
- miR-124-3p overexpression reduced PKC-δ expression and phosphorylation.
- Overexpression of miR-124-3p inhibited migration, invasion, EMT, and stemness, mimicking PKC inhibition effects.
Conclusions:
- A novel miR-124-3p/PKC-δ axis negatively regulates PKC-δ signaling in bladder cancer.
- This axis suppresses bladder cancer progression, indicating potential therapeutic value.
