Jung Heung-Su, Kwon Byung-Su, Lee Seong-Wook
Department of Molecular Biology, Institute of Nanosensor and Biotechnology, Dankook University, Seoul, 140-714, Korea.
Biotechnol Lett. 2005 Apr;27(8):567-74. doi: 10.1007/s10529-005-2883-6.
Current gene therapy protocols against cancer often have limited target specificity. Here, a novel tumor-specific targeted gene delivery procedure, which is based on Tetrahymena group I intron ribozyme, is presented. This ribozyme can target a cancer-specific transcript and then replace the RNA with new transcripts, resulting in induction of the transgene activity selectively in cancer cells that express the target RNA. The RNA replacement occurs by trans-splicing reaction with high fidelity with the target RNA. In addition, the ribozyme can specifically inhibit function of the targeted gene in the cells expressing the RNA. Moreover, the ribozyme can selectively deliver cytotoxin gene activity into cancer cells expressing the RNA and thereby specifically hampers the survival of these cells. These findings suggest that the trans-splicing ribozyme that targets the cancer-specific RNA could be a potential agent for specific tumor gene therapy.
当前针对癌症的基因治疗方案往往具有有限的靶向特异性。在此,我们提出了一种基于四膜虫I组内含子核酶的新型肿瘤特异性靶向基因递送方法。这种核酶可以靶向癌症特异性转录本,然后用新的转录本替换RNA,从而在表达靶RNA的癌细胞中选择性地诱导转基因活性。RNA替换通过与靶RNA的转剪接反应以高保真度发生。此外,核酶可以在表达RNA的细胞中特异性抑制靶向基因的功能。而且,核酶可以将细胞毒素基因活性选择性地递送到表达RNA的癌细胞中,从而特异性地阻碍这些细胞的存活。这些发现表明,靶向癌症特异性RNA的转剪接核酶可能是一种潜在的特异性肿瘤基因治疗药物。