Chmura S J, Gupta N, Advani S J, Kufe D W, Weichselbaum R R
Department of Radiation and Cellular Oncology, University of Chicago, Chicago, IL 60637, USA.
Semin Radiat Oncol. 2001 Oct;11(4):338-45. doi: 10.1053/srao.2001.26019.
Ionizing radiation (IR) has been extensively used to treat a variety of solid tumors to improve local control and overall survival in patients. Gene therapy strategies represent one experimental direction to improve radiocurability. These gene therapy strategies include (1) replacement of mutated or deleted tumor-suppressor genes, (2) delivery of prodrugs, (3) transduction of genes under the control of radiation-inducible promoters, and (4) genetically engineered viruses that replicate preferentially in tumor cells after IR. Although any one of these viral-based gene therapy approaches is unlikely to succeed independently, experimental results suggest that clinically important antitumor can be achieved when these strategies are combined with IR. Several of these strategies are currently being or soon will be evaluated in clinical trials. This review focuses on molecular mechanisms and potential clinical application of these viral-based gene therapy strategies to improve the therapeutic index of IR.
电离辐射(IR)已被广泛用于治疗各种实体瘤,以提高患者的局部控制率和总生存率。基因治疗策略是提高放射可治愈性的一个实验方向。这些基因治疗策略包括:(1)替换突变或缺失的肿瘤抑制基因;(2)递送前药;(3)转导受辐射诱导启动子控制的基因;(4)基因工程病毒,其在IR后优先在肿瘤细胞中复制。尽管这些基于病毒的基因治疗方法中的任何一种都不太可能独立成功,但实验结果表明,当这些策略与IR联合使用时,可以实现具有临床意义的抗肿瘤效果。目前,这些策略中的几种正在或即将在临床试验中进行评估。本综述重点关注这些基于病毒的基因治疗策略的分子机制及其潜在的临床应用,以提高IR的治疗指数。