Grill Jacques, Geoerger Birgit, Lamfers Martine, Dirven Clemens, Van Beusechem Victor, Gerritsen Winald, Vassal Gilles
UPRES EA 3535, Pharmacologie et nouveaux traitements des cancers, Institut Gustave-Roussy, 94805 Villejuif.
Bull Cancer. 2003 Dec;90(12):1039-48.
Cancer gene therapy has offered many hopes but its first use in humans revealed some pitfalls and at least three main problems: lack of efficacy and specificity of current vectors to deliver therapeutic genes, poor diffusion of the therapeutic effects inside the tumor (absence of bystander effect), poor distribution of the vectors injected inside the tissue. To address some of these issues, several teams have developed tumor selective replicating adenoviruses, some of them being already in the clinic. First results are promising but complementary studies are needed to define if these agents will take place in the therapeutic armentorium against cancer.
癌症基因治疗带来了诸多希望,但其首次应用于人体时暴露出一些缺陷以及至少三个主要问题:当前用于递送治疗性基因的载体缺乏有效性和特异性、治疗效果在肿瘤内部的扩散不佳(不存在旁观者效应)、注射到组织内的载体分布不均。为解决其中一些问题,多个团队已研发出肿瘤选择性复制腺病毒,其中一些已进入临床试验阶段。初步结果很有前景,但仍需补充研究以确定这些药物是否会纳入抗癌治疗手段之中。