IMPROVING SUICIDE GENES FOR CANCER GENE THERAPY

改善自杀基因以进行癌症基因治疗

• 批准号: 6633697
• 负责人: MARGARET E BLACK
• 金额: $ 19.31万
• 依托单位: WASHINGTON STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-05-11 至 2005-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6633697
• 关键词: aminohydrolases; chemical models; chimeric proteins; combination cancer therapy; fusion gene; gene mutation; gene therapy; herpes simplex virus 1; laboratory mouse; model design /development; neoplasm /cancer therapy; prodrugs; site directed mutagenesis; thymidine kinase; tissue /cell culture

Gene therapy offers the prospect of selectively introducing genes into cancer cells, leaving them susceptible to specific antitumor drugs. Current protocols to elicit tumor reduction utilize Herpes Simplex Virus type 1(HSV) thymidine kinase (TK) with the prodrug ganciclovir (GCV) or the E. coli cytosine deaminase with the prodrug 5-fluorocytosine (5FC). While the wild-type TK is functional as a suicide gene, a number of caveats restrict its full effectiveness. These include a poor Km or binding affinity for GCV (approximately 47muM) and the toxicity associated with high doses of GCV. Another prodrug, acyclovir (ACV), predominantly used as an anti-herpetic drug, does not demonstrate the immunosuppressive attributes of GCV, even at very high doses. However, the very high Km that HSV TK displays towards ACV (approximately 320 muM), precludes its use as a prodrug in ablative gene therapy. Similarly, there are caveats with cytosine deaminase and 5FC that preclude its potential as a safe and effective suicide gene. We seek to identify the optimal suicide gene and prodrug combination for the safest and most effective cancer gene therapy. Towards this end we seek 1) to understand the structure-function relationship of nucleoside metabolizing enzymes important to suicide gene therapy and 2) to manipulate HSV-1 thymidine kinase and cytosine deaminase genes for superior performance in ablative gene therapy settings. The goal of this work is to 1) create novel genes by mutagenesis, 2) evaluate mutant genes for improved tumor sensitivity to various prodrugs, 3) construct mini-pathways and 4) create fusion proteins with other genes to enhance prodrug activation and tumor ablation. Not only will the results from the project impact the choice of gene(s) used for cancer treatment, but it also has wide-reaching applications including graft versus host disease, restenosis, AIDS, tumor imaging, cell lineage ablation studies, in negative selection systems and selection against non-homologous recombination for the generation of transgenic mice. Furthermore, understanding the molecular basis of nucleoside metabolizing enzyme function and interaction with current drugs will have far-reaching ramifications in the design, development and use of novel antiviral, antifungal and antibacterial drugs.

基因治疗提供了选择性地将基因导入癌细胞的前景，使它们对特定的抗肿瘤药物敏感。 目前引起肿瘤缩小的方案利用单纯疱疹病毒1型（HSV）胸苷激酶（TK）与前药更昔洛韦（GCV）或E.大肠杆菌胞嘧啶脱氨酶与前体药物5-氟胞嘧啶（5 FC）。 虽然野生型TK具有自杀基因的功能，但一些注意事项限制了其完全有效性。 这些包括对GCV的Km或结合亲和力差（约47 μ M）和与高剂量GCV相关的毒性。 另一种主要用作抗疱疹药物的前体药物阿昔洛韦（ACV），即使在非常高的剂量下也没有表现出GCV的免疫抑制属性。然而，HSV TK对ACV显示出非常高的Km（约320 μ M），排除了其在消融基因治疗中作为前药的用途。 同样，胞嘧啶脱氨酶和5 FC也存在一些问题，这些问题排除了其作为安全有效的自杀基因的潜力。我们寻求确定最佳的自杀基因和前药组合的最安全和最有效的癌症基因治疗。 为此，我们寻求1）了解对自杀基因治疗重要的核苷代谢酶的结构-功能关系和2）操纵HSV-1胸苷激酶和胞嘧啶脱氨酶基因，以在消融基因治疗环境中获得上级性能。 这项工作的目标是1）通过诱变产生新的基因，2）评估突变基因以改善肿瘤对各种前药的敏感性，3）构建微通路，4）与其他基因产生融合蛋白以增强前药活化和肿瘤消融。该项目的结果不仅将影响用于癌症治疗的基因的选择，而且还具有广泛的应用，包括移植物抗宿主病，再狭窄，艾滋病，肿瘤成像，细胞谱系消融研究，在阴性选择系统和针对非同源重组的选择中产生转基因小鼠。此外，了解核苷代谢酶功能的分子基础以及与现有药物的相互作用将对新型抗病毒、抗真菌和抗细菌药物的设计、开发和使用产生深远的影响。