Weichselbaum R R, Kufe D W, Advani S J, Roizman B
Department of Radiation and Cellular Oncology, The Pritzker School of Medicine, The University of Chicago, Illinois 60637, USA.
Acta Oncol. 2001;40(6):735-8. doi: 10.1080/02841860152619151.
The full promise of gene therapy has been limited by the lack of specificity of vectors for tumor tissue as well as the lack of antitumor efficacy of transgenes encoded by gene delivery systems. In this paper we review our studies investigating two modifications of gene therapy combined with radiotherapy. The first investigations described include studies of radiation inducible gene therapy. In this paradigm, radio-inducible DNA sequences from the CarG elements of the Egr-1 promoter are cloned upstream of a cDNA encoding TNFalpha. The therapeutic gene (TNFalpha) is induced by radiation within the tumor microenvironment. In the second paradigm, genetically engineered herpes simplex virus (HSV-1) is induced by ionizing radiation to proliferate within the tumor volume. These modifications of radiotherapy and gene therapy may enhance the efficacy of both treatments.
基因治疗的全部潜力受到载体对肿瘤组织缺乏特异性以及基因递送系统所编码转基因的抗肿瘤功效不足的限制。在本文中,我们回顾了我们对两种基因治疗与放射治疗相结合的研究。所描述的首批研究包括辐射诱导基因治疗的研究。在这种模式中,来自Egr-1启动子的CarG元件的辐射诱导DNA序列被克隆到编码肿瘤坏死因子α(TNFα)的cDNA上游。治疗性基因(TNFα)在肿瘤微环境中由辐射诱导。在第二种模式中,基因工程改造的单纯疱疹病毒(HSV-1)由电离辐射诱导在肿瘤体积内增殖。放射治疗和基因治疗的这些改进可能会提高两种治疗的疗效。