Related Experiment Video
Updated: Mar 15, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
miR-451 suppresses bladder cancer cell migration and invasion via directly targeting c-Myc
Jun Wang1, Xiaomei Zhao1, Jianhua Shi1
1Department of Urology, The First Clinical Medical School of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Abstract:
MicroRNA (miRNA) expression is shown dysregulated in tumors. It has been reported that miR-451 alters gene expression and regulates tumorigenesis in various cancer tissues. However, its underlying biological significance in bladder cancer remains to be clarified. In the present study, we investigated the function and molecular mechanism of miR-451 involved in bladder cancer cell migration and invasion. Our results showed that miR-451 was downregulated in clinical bladder carcinoma tissues compared with adjacent bladder tissues. Overexpression of miR-451 significantly retarded the proliferation, migration and invasion of bladder cancer T24 and 5637 cells in vitro. Moreover, the attenuated cell migration and invasion by miR-451 was correlated with increased apoptosis. However, our dual-luciferase reporter assay validated that c-Myc, an oncogene in many tumors, was a direct target gene of miR-451 in bladder cancer. The expression of c-Myc was repressed by miR-451 in bladder cancer cells, and knockdown of c-Myc mimicked the effects of miR-451 overexpression. This discovery suggested that miR-451 is a tumor suppressor modulating bladder cancer cell migration and invasion by directly targeting c-Myc. In addition, apoptosis promoted by miR-451 may participates in this biological behavior. Therefore, target miR-451 may be a novel therapeutic intervention for bladder cancer.
Insights
MicroRNA-451 (miR-451) acts as a tumor suppressor in bladder cancer by inhibiting cell migration and invasion. It targets the oncogene c-Myc, offering a potential therapeutic strategy for bladder cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miRNA) dysregulation is common in tumors, affecting gene expression and tumorigenesis.
- The specific role of miR-451 in bladder cancer progression requires further investigation.
Purpose of the Study:
- To investigate the function and molecular mechanism of miR-451 in bladder cancer cell migration and invasion.
- To determine if miR-451 acts as a tumor suppressor in bladder cancer.
Main Methods:
- Quantitative analysis of miR-451 expression in clinical bladder cancer tissues.
- In vitro experiments assessing the effects of miR-451 overexpression on bladder cancer cell proliferation, migration, invasion, and apoptosis.
- Dual-luciferase reporter assays to validate c-Myc as a direct target of miR-451.
- c-Myc knockdown experiments to confirm its role.
Main Results:
- miR-451 was significantly downregulated in bladder carcinoma tissues.
- Overexpression of miR-451 suppressed bladder cancer cell proliferation, migration, and invasion, and increased apoptosis.
- miR-451 directly targets and represses c-Myc expression in bladder cancer cells.
- Knockdown of c-Myc replicated the inhibitory effects of miR-451 overexpression.
Conclusions:
- miR-451 functions as a tumor suppressor in bladder cancer by inhibiting cell migration and invasion, partly through direct targeting of c-Myc.
- miR-451-induced apoptosis may contribute to its tumor-suppressive effects.
- Targeting miR-451 presents a potential novel therapeutic strategy for bladder cancer.
Related Concept Videos
Induced Pluripotent Stem Cells
Somatic...
Abnormal Proliferation
MicroRNAs
MicroRNAs
Targeted Cancer Therapies
There are several types of targeted therapies against...

