Antitumor efficacy of regional oncolytic viral therapy for peritoneally disseminated cancer

被引:50
作者
Bennett, JJ
Kooby, DA
Delman, K
McAuliffe, P
Halterman, MW
Federoff, H
Fong, YM
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10021 USA
[2] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Neurosci, Rochester, NY 14642 USA
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2000年 / 78卷 / 03期
关键词
peritoneal tumor; herpes simplex virus; stomach cancer; gene therapy;
D O I
10.1007/s001090000092
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Oncolytic viral therapy is a promising new method of cancer treatment. Peritoneal dissemination of cancer is a common and fatal clinical condition seen in many malignancies, with few effective therapies available. G207, a multimutated replication-competent herpes simplex virus type-1, effectively treats disseminated peritoneal cancer This study evaluates viral proliferation and subsequent tumoricidal effects in vitro and in vivo after regional viral delivery. In vitro studies demonstrate that G207 efficiently kills five human gastric cancer cell lines, and that permissiveness to viral replication is correlated with cytotoxicity. In a murine xenograft model of human gastric carcinomatosis, peritoneal delivery of G207 effectively kills tumor and prolongs survival. Data from quantitative PCR characterizes peritoneal clearance of virus after intraperitoneal injection, and identifies G207 replication within tumor cells in vivo, similar to in vitro proliferation. Further analysis of various organs confirms that G207 does not replicate within normal tissue after peritoneal delivery. Wild-type KOS viral replication was also demonstrated in vivo, with significant toxicity secondary to dissemination and encephalitis. In vivo viral proliferation of G207 is restricted to tumor cells, is correlated with in vitro assays, and is an important mechanism of anticancer efficacy.
引用
收藏
页码:166 / 174
页数:9
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