Fillat C, Carrió M, Cascante A, Sangro B
Programa Gens i Malaltia, Centre de Regulació Genòmica, Barcelona, Spain.
Curr Gene Ther. 2003 Feb;3(1):13-26. doi: 10.2174/1566523033347426.
Gene-directed enzyme prodrug therapy (GDEPT) is a two step therapeutic approach for cancer gene therapy. In the first step, the transgene is delivered into the tumor and expressed. In the second step a prodrug is administered and is selectively activated by the expressed enzyme. The first GDEPT system described was the thymidine kinase gene of the Herpes Simplex virus (HSVtk) in combination with the prodrug Ganciclovir (GCV). A large number of experiments have been performed with this system, in different types of tumors and initial studies in animal models were very promising. This encouraged investigators to move into clinical trials although poor results have been obtained so far. A large effort has been made with numerous different strategies to enhance HSVtk/GCV efficacy in cellular and in vivo models and very strong cytotoxic effects have been obtained. The present review describes the current state of preclinical research and summarizes the results of the clinical trials undertaken.
基因导向酶前药疗法(GDEPT)是癌症基因治疗的两步治疗方法。第一步,将转基因导入肿瘤并表达。第二步,给予前药,其被表达的酶选择性激活。所描述的第一个GDEPT系统是单纯疱疹病毒(HSVtk)的胸苷激酶基因与前药更昔洛韦(GCV)结合。已用该系统在不同类型肿瘤中进行了大量实验,动物模型的初步研究很有前景。这鼓励研究人员开展临床试验,尽管迄今为止结果不佳。人们采用了许多不同策略,在细胞和体内模型中大力提高HSVtk/GCV的疗效,并已获得非常强的细胞毒性作用。本综述描述了临床前研究的现状,并总结了所进行的临床试验结果。