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Updated: Jan 5, 2026

An In Vitro Protocol for Evaluating MicroRNA Levels, Functions, and Associated Target Genes in Tumor Cells
Published on: May 21, 2019
MicroRNA-34a inhibits bladder cancer cell migration and invasion, and upregulates PTEN expression
Zhen-Shan Ding1, Yu-Hui He2, Yi-Sen Deng2
1Department of Urology, China-Japan Friendship Hospital, Beijing 100029, P.R. China.
Abstract:
MicroRNA-34a (miR-34a) serves as a tumor suppressor in a number of different types of cancer. The present study was performed to investigate the involvement of miR-34a in bladder cancer. In the present study, miR-34a was downregulated in patients with bladder cancer compared with the healthy controls in bladder biopsies and plasma. Downregulation of miR-34a distinguished between patients with bladder cancer and the healthy controls. miR-34a expression was associated with tumor metastasis; however, not with tumor size. Transfection of miR-34a mimics upregulated the expression of phosphatase and tensin homolog (PTEN) in bladder cancer cells, and decreased cell migration and invasion. miR-34a may inhibit bladder cancer cell migration and invasion by upregulating PTEN. miR-34a may additionally serve as a potential therapeutic target for bladder cancer.
Insights
MicroRNA-34a (miR-34a) is downregulated in bladder cancer patients, distinguishing them from healthy individuals. This microRNA may suppress bladder cancer progression by upregulating PTEN, inhibiting cell migration and invasion.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-34a (miR-34a) is recognized for its tumor suppressor role across various cancers.
- Its specific involvement in bladder cancer pathogenesis requires further elucidation.
Purpose of the Study:
- To investigate the role and expression of miR-34a in bladder cancer.
- To explore the potential mechanism of miR-34a in regulating bladder cancer cell behavior.
Main Methods:
- Comparative analysis of miR-34a expression in bladder cancer tissues and plasma versus healthy controls.
- Functional assays involving transfection of miR-34a mimics in bladder cancer cells.
- Assessment of phosphatase and tensin homolog (PTEN) expression and cell migration/invasion after miR-34a mimic transfection.
Main Results:
- miR-34a was significantly downregulated in bladder cancer patients (biopsies and plasma) compared to healthy controls.
- Downregulation of miR-34a correlated with tumor metastasis but not tumor size.
- Upregulation of miR-34a via mimics increased PTEN expression and reduced bladder cancer cell migration and invasion.
Conclusions:
- miR-34a is downregulated in bladder cancer and can serve as a biomarker for disease detection.
- miR-34a inhibits bladder cancer cell migration and invasion, potentially through PTEN upregulation.
- miR-34a represents a promising therapeutic target for bladder cancer treatment.
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