Ovarian cancer gene therapy: Repeated treatment with thymidine kinase in an adenovirus vector and ganciclovir improves survival in a novel immunocompetent murine model

被引:33
作者
Al-Hendy, A
Magliocco, AM
Al-Tweigeri, T
Braileanu, G
Crellin, N
Li, H
Strong, T
Curiel, D
Chedrese, PJ
机构
[1] Univ Saskatchewan, Dept Obstet Gynecol & Reprod Sci, Saskatoon, SK S7N 0W8, Canada
[2] Univ Saskatchewan, Dept Pathol, Saskatoon, SK S7N 0W8, Canada
[3] Univ Saskatchewan, Ctr Canc, Saskatoon, SK S7N 0W8, Canada
[4] Univ Alabama, Ctr Comprehens Canc, Birmingham, AL 35294 USA
基金
英国医学研究理事会;
关键词
adenovirus; antibodies; gene therapy; ovarian cancer;
D O I
10.1067/mob.2000.104837
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Our purpose was to assess the effect of multiple injections of the system of herpes simplex virus thymidine kinase in an adenovirus vector and ganciclovir on survival in a murine model of human epithelial ovarian cancer. STUDY DESIGN: In this work we tested the ability of the system of thymidine kinase delivered by an adenovirus vector and ganciclovir to treat ovarian cancer in a novel murine model for epithelial ovarian cancer, SaskMouse. SaskMouse was developed by injecting LM-1 cells, a murine epithelial ovarian cancer cell line, intraperitoneally into a syngeneic C57BL/6N x C3H/He mouse strain. The cells developed into multiple cancer implants on different abdominal organs, leading to ascites and rapid death. The model has an intact immune system, as evidenced by the inability of different human cancer cells to develop into cancers when injected into the mice intraperitoneally. RESULTS: The system of thymidine kinase delivered by an adenovirus vector and ganciclovir was applied to SaskMouse. Mice were either untreated (group 1), treated with one intraperitoneal injection of adenovirus-thymidine kinase at 250 plaque-forming units/cell (group 2), or treated with two intraperitoneal injections of adenovirus-thymidine kinase at 250 plaque-forming units/cell on days 0 and 23 (group 3). Survivals were 23 +/- 2, 27 +/- 2, and 35 +/- 4 days, respectively (P <.05). Antiadenoviral antibodies were assayed both in the serum and in the peritoneal fluid of treated mice. Despite high antibody titers in serum, there were no detectable antibodies in the peritoneal fluid. CONCLUSION: Our data suggest that multiple intraperitoneal injections of the combination of thymidine kinase delivered by an adenovirus Vector and ganciclovir are effective in prolonging survival in the presence of ovarian cancer. There are potential implications for other abdominal malignancies.
引用
收藏
页码:553 / 559
页数:7
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