Abstract
Ovarian cancer is a major clinical problem with no rewarding treatment protocol currently available. In other malignancies transfer of the herpes simplex virus thymidine kinase (HSV-tk) gene into tumor cells using a viral vector followed by administration of ganciclovir (GCV) provides a potentially effective strategy for treatment. In this work human ovarian epithelial cancer cell lines were infected with a recombinant adenoviral vector expressing the HSV-tk (AdRSV-tk) and were rendered sensitive to doses of GCV that were 100-200 times less than for untransfected cells. A strong bystander effect was noted with significant killing at a ratio of infected:uninfected cells of only 1:20 and maximal killing at 1:3. Normal human ovarian surface epithelial cells were also highly sensitive to the AdRSV-tk/GCV system. This study demonstrates the potential efficacy of the HSV-tk/GCV approach in ovarian cancer gene therapy.
Original language | English (US) |
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Pages (from-to) | 268-275 |
Number of pages | 8 |
Journal | Gynecologic and Obstetric Investigation |
Volume | 43 |
Issue number | 4 |
DOIs | |
State | Published - Jan 1 1997 |
Keywords
- Adenovirus
- Ganciclovir
- Gene therapy
- Ovarian cancer
- Thymidine kinase
ASJC Scopus subject areas
- Reproductive Medicine
- Obstetrics and Gynecology