Biederer Carola, Ries Stefan, Brandts Christian H, McCormick Frank
SWITCH Biotech AG, Fraunhofer Strasse 10, 82152 Martinsried, Germany.
J Mol Med (Berl). 2002 Mar;80(3):163-75. doi: 10.1007/s00109-001-0295-1. Epub 2001 Dec 20.
Advances in our understanding of the molecular basis of cancer and the availability of technology to genetically engineer viruses have led to the development of replication-competent viruses to treat cancer. In theory, replication-selective viruses offer several appealing properties as biological agents for cancer therapy: they kill tumor cells selectively, and their replication leads to amplification of their oncolytic potential. Most preclinical experiments in tissue culture and in animal models support this notion. Clinical data on the first generation of replication-selective viruses are now rapidly accruing. The therapeutic index, and ultimately the clinical outcome, will depend on a complex balance between host and viral factors. This review discusses strategies to kill cancer cells based on our understanding of their molecular defects and the progress being made using replication-competent viruses for tumor therapy. We focus our discussion on a replication-selective adenovirus called ONYX-015 that has recently demonstrated encouraging results in clinical trials
我们对癌症分子基础认识的进展以及基因工程改造病毒技术的出现,促使了具有复制能力的病毒用于癌症治疗的发展。理论上,复制选择性病毒作为癌症治疗的生物制剂具有几个吸引人的特性:它们能选择性地杀死肿瘤细胞,并且其复制会导致溶瘤潜力的放大。大多数组织培养和动物模型中的临床前实验都支持这一观点。关于第一代复制选择性病毒的临床数据现在正在迅速积累。治疗指数以及最终的临床结果将取决于宿主和病毒因素之间的复杂平衡。本综述基于我们对癌细胞分子缺陷的理解,讨论了杀死癌细胞的策略以及使用具有复制能力的病毒进行肿瘤治疗所取得的进展。我们将讨论重点放在一种名为ONYX - 015的复制选择性腺病毒上,该病毒最近在临床试验中显示出令人鼓舞的结果