BACKGROUND AND OBJECTIVES: Many genetically engineered viruses have been evaluated for their potential as therapeutic agents in the treatment of malignant tumors. We applied a spontaneously generated, highly attenuated herpes simplex virus (HSV) type-1 clone, HF10, to the treatment of breast cancer. In this study, we investigated the ability of HF10 to infect and lyse human and murine breast cancer cells in vitro and tested its efficacy in an immuno-competent animal model of breast cancer. METHODS: To assess the therapeutic efficacy of HF10 against subcutaneous tumors in vivo, mouse breast cancer cells were injected into the backs of mice, which were then treated with HF10. Tumor volume and survival rate were used as measures of the antitumor effect in the in vivo experiments. In vitro viral cytotoxity assays and replication assays were also performed in human breast cancer cell lines. RESULTS: In the in vivo study, tumor growth was suppressed and long-term survival rates were prolonged. HF10 was effective in producing cytolytic effects in vitro at various multiplicities of infection (MOI) in all cell lines tested. CONCLUSIONS: HF10 demonstrated antitumor effects in our animal model. The viral growth and oncolytic effect of HF10 in the human breast cancer cell line suggest that HF10 is potentially effective in the clinical treatment of human cancer. These results indicate that replication-competent HSV-1 mutants hold significant promise as cancer therapeutic agents. Copyright 2003 Wiley-Liss, Inc.
BACKGROUND AND OBJECTIVES: Many genetically engineered viruses have been evaluated for their potential as therapeutic agents in the treatment of malignant tumors. We applied a spontaneously generated, highly attenuated herpes simplex virus (HSV) type-1 clone, HF10, to the treatment of breast cancer. In this study, we investigated the ability of HF10 to infect and lyse human and murinebreast cancer cells in vitro and tested its efficacy in an immuno-competent animal model of breast cancer. METHODS: To assess the therapeutic efficacy of HF10 against subcutaneous tumors in vivo, mousebreast cancer cells were injected into the backs of mice, which were then treated with HF10. Tumor volume and survival rate were used as measures of the antitumor effect in the in vivo experiments. In vitro viral cytotoxity assays and replication assays were also performed in humanbreast cancer cell lines. RESULTS: In the in vivo study, tumor growth was suppressed and long-term survival rates were prolonged. HF10 was effective in producing cytolytic effects in vitro at various multiplicities of infection (MOI) in all cell lines tested. CONCLUSIONS:HF10 demonstrated antitumor effects in our animal model. The viral growth and oncolytic effect of HF10 in the humanbreast cancer cell line suggest that HF10 is potentially effective in the clinical treatment of humancancer. These results indicate that replication-competent HSV-1 mutants hold significant promise as cancer therapeutic agents. Copyright 2003 Wiley-Liss, Inc.
Authors: S Fujiwara; A Nawa; C Luo; M Kamakura; F Goshima; C Kondo; T Kiyono; F Kikkawa; Y Nishiyama Journal: Cancer Gene Ther Date: 2010-10-01 Impact factor: 5.987