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Updated: Aug 4, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Tissue-specific promoters in gene therapy for the treatment of prostate cancer
1Department of Urology, Kobe University School of Medicine, Kobe, Japan. toshiro@kobe-u.ac.jp
Abstract:
Delivery of therapeutic toxic genes to and their expression in tumor cells through the use of tissue-specific promoters could decrease their toxic effect on neighboring normal cells when virus-mediated gene delivery results in their infection. We have demonstrated the utility of two prostate cancer-specific promoters, long PSA and osteocalcin, for tissue-specific toxic gene therapy for prostate cancer. The two promoters were highly active in both androgen-dependent and androgen-independent prostate cancer cells. We also introduce the Phase I trial of osteocalcin promoter-based toxic gene therapy for bone metastases of prostate cancer, which is in progress at the University of Virginia.
Insights
This study shows prostate cancer-specific promoters can target toxic gene therapy to tumors, reducing harm to normal cells. A Phase I trial is underway for bone metastases using this approach.
Area of Science:
- Oncology
- Gene Therapy
- Molecular Biology
Background:
- Virus-mediated gene delivery can harm normal cells.
- Tissue-specific promoters offer targeted therapeutic gene expression.
- Prostate cancer presents challenges for localized treatment.
Purpose of the Study:
- To evaluate prostate cancer-specific promoters for targeted toxic gene therapy.
- To assess promoter activity in different prostate cancer cell types.
- To introduce a Phase I clinical trial for osteocalcin promoter-based therapy.
Main Methods:
- Utilized long PSA and osteocalcin promoters.
- Tested promoter activity in androgen-dependent and independent prostate cancer cells.
- Initiated a Phase I clinical trial for bone metastases.
Main Results:
- Both long PSA and osteocalcin promoters showed high activity in prostate cancer cells.
- Demonstrated utility for tissue-specific toxic gene therapy.
- Confirmed promoter activity across different cancer cell dependencies.
Conclusions:
- Prostate cancer-specific promoters are effective for targeted toxic gene therapy.
- Osteocalcin promoter shows promise for treating bone metastases.
- Ongoing Phase I trial will further validate this therapeutic strategy.
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