Department of Clinical Neuroscience, Karolinska Institutet, Center for Molecular Medicine, KarolinskaUniversity Hospital, Stockholm, Sweden.
Neuro Oncol. 2010 Jun;12(6):549-58. doi: 10.1093/neuonc/nop067. Epub 2010 Feb 13.
The prognosis for malignant gliomas remains poor, and new treatments are urgently needed. Targeted suicide gene therapy exploits the enzymatic conversion of a prodrug, such as a nucleoside analog, into a cytotoxic compound. Although this therapeutic strategy has been considered a promising regimen for central nervous system (CNS) tumors, several obstacles have been encountered such as inefficient gene transfer to the tumor cells, limited prodrug penetration into the CNS, and inefficient enzymatic activity of the suicide gene. We report here the cloning and successful application of a novel thymidine kinase 1 (TK1) from the tomato plant, with favorable characteristics in vitro and in vivo. This enzyme (toTK1) is highly specific for the nucleoside analog prodrug zidovudine (azidothymidine, AZT), which is known to penetrate the blood-brain barrier. An important feature of toTK1 is that it efficiently phosphorylates its substrate AZT not only to AZT monophosphate, but also to AZT diphosphate, with excellent kinetics. The efficiency of the toTK1/AZT system was confirmed when toTK1-transduced human glioblastoma (GBM) cells displayed a 500-fold increased sensitivity to AZT compared with wild-type cells. In addition, when neural progenitor cells were used as delivery vectors for toTK1 in intracranial GBM xenografts in nude rats, substantial attenuation of tumor growth was achieved in animals exposed to AZT, and survival of the animals was significantly improved compared with controls. The novel toTK1/AZT suicide gene therapy system in combination with stem cell-mediated gene delivery promises new treatment of malignant gliomas.
恶性神经胶质瘤的预后仍然很差,急需新的治疗方法。靶向自杀基因治疗利用酶将前体药物(如核苷类似物)转化为细胞毒性化合物。尽管这种治疗策略被认为是中枢神经系统(CNS)肿瘤的一种有前途的治疗方案,但仍遇到了一些障碍,例如基因向肿瘤细胞的转移效率低、前体药物向 CNS 的渗透有限以及自杀基因的酶活性效率低。我们在此报告从番茄植物中克隆并成功应用了一种新型胸苷激酶 1(TK1),该酶具有体外和体内的良好特性。这种酶(toTK1)对核苷类似物前体药物齐多夫定(叠氮胸苷,AZT)具有高度特异性,AZT 已知可穿透血脑屏障。toTK1 的一个重要特征是,它不仅能有效地将其底物 AZT 磷酸化为 AZT 单磷酸,还能磷酸化为 AZT 二磷酸,具有极好的动力学。当转染 toTK1 的人神经胶质瘤(GBM)细胞对 AZT 的敏感性比野生型细胞增加了 500 倍时,toTK1/AZT 系统的效率得到了证实。此外,当神经祖细胞作为转染 toTK1 的载体用于裸鼠颅内 GBM 异种移植时,暴露于 AZT 的动物的肿瘤生长明显减弱,与对照组相比,动物的存活率显著提高。新型 toTK1/AZT 自杀基因治疗系统与干细胞介导的基因传递相结合,有望为恶性神经胶质瘤提供新的治疗方法。