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Updated: Jun 17, 2026

An Orthotopic Bladder Tumor Model and the Evaluation of Intravesical saRNA Treatment
Published on: July 28, 2012
Androgen receptor is a potential therapeutic target for bladder cancer
Ji-Tao Wu1, Bang-Min Han, Sheng-Qiang Yu
1Department of Urology, First People's Hospital Affiliated to Shanghai, Jiao Tong University, Shanghai, China.
Objectives:
To investigate whether androgen receptor (AR) could serve as a potential molecular target for the treatment of bladder cancer.
Methods:
Cell proliferation, apoptosis, and migration capacity were determined in human transitional carcinoma cell lines T24 and 253-J treated with small interfering RNA directed against AR, and expression levels of growth- and metastasis-related genes were assessed using quantitative reverse transcriptase-polymerase chain reaction. Tumor cell growth and apoptosis were also evaluated in vivo in T24 tumor-bearing nude mice receiving electroporation-assisted administration of anti-AR small interfering RNA.
Results:
AR expression knockdown produced increased apoptosis, decreased proliferation, and migration of bladder cancer cells. Cyclin D1, Bcl-x(L), and matrix metallopeptidase-9 gene expression were also reduced with AR knockdown, which might have contributed to the altered biological behavior of cancer cells. In vivo experiments showed that silencing AR expression, by interference aided by electroporation, significantly suppressed AR-positive bladder tumor growth with decreased cell proliferation and increased apoptotic rates.
Conclusions:
Downregulation of AR expression inhibits bladder cancer cell growth in vitro and in vivo, implying that its use might be a potential therapeutic target for the treatment of bladder cancer.
Insights
Targeting the androgen receptor (AR) significantly inhibits bladder cancer growth by reducing proliferation and increasing apoptosis. This suggests AR is a potential therapeutic target for bladder cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Bladder cancer remains a significant health concern with limited targeted therapies.
- The androgen receptor (AR) plays a role in various cancers, but its specific role in bladder cancer requires further investigation.
Purpose of the Study:
- To determine if the androgen receptor (AR) can be a viable molecular target for treating bladder cancer.
- To investigate the effects of AR downregulation on bladder cancer cell behavior and tumor growth.
Main Methods:
- Utilized human transitional carcinoma cell lines (T24 and 253-J) treated with small interfering RNA (siRNA) targeting AR.
- Assessed cell proliferation, apoptosis, and migration in vitro.
- Quantified expression of growth and metastasis-related genes using quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR).
- Evaluated tumor growth and apoptosis in vivo using T24 tumor-bearing nude mice treated with electroporation-assisted anti-AR siRNA.
Main Results:
- AR expression knockdown led to increased apoptosis, reduced proliferation, and inhibited migration of bladder cancer cells.
- Silencing AR decreased the expression of Cyclin D1, Bcl-x(L), and matrix metallopeptidase-9.
- In vivo studies demonstrated that AR silencing significantly suppressed tumor growth, decreased proliferation, and increased apoptosis in AR-positive bladder tumors.
Conclusions:
- Downregulation of AR expression effectively inhibits bladder cancer cell growth both in vitro and in vivo.
- These findings indicate that the androgen receptor (AR) is a promising therapeutic target for bladder cancer treatment.
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