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Cancer Specificity of Promoters of the Genes Involved in Cell Proliferation Control

机译:参与细胞增殖控制的基因启动子的癌症特异性

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摘要

Core promoters with adjacent regions of the human genes CDC6, POLD1, CKS1B, MCM2, and PLK1 were cloned into a pGL3 vector in front of the Photinus pyrails gene Luc in order to study the tumor specificity of the promoters. The cloned promoters were compared in their ability to direct luciferase expression in different human cancer cells and in normal fibroblasts. The cancer-specific promoter BIRC5 and non-specific CMV immediately early gene promoter were used for comparison. All cloned promoters were shown to be substantially more active in cancer cells than in fibroblasts, while the PLK1 promoter was the most cancer-specific and promising one. The specificity of the promoters to cancer cells descended in the series PLK1, CKS1B, POLD1, MCM2, and CDC6. The bidirectional activity of the cloned CKS1B promoter was demonstrated. It apparently directs the expression of the SHC1 gene, which is located in a “head-to-head” position to the CKS1B gene in the human genome. This feature should be taken into account in future use of the CKS1B promoter. The cloned promoters may be used in artificial genetic constructions for cancer gene therapy.
机译:将人类基因CDC6,POLD1,CKS1B,MCM2和PLK1相邻区域的核心启动子克隆到Photinus pyrails基因Luc前面的pGL3载体中,以研究启动子的肿瘤特异性。比较了克隆的启动子在不同人类癌细胞和正常成纤维细胞中指导荧光素酶表达的能力。使用癌症特异性启动子BIRC5和非特异性CMV立即早期基因启动子进行比较。已显示所有克隆的启动子在癌细胞中的活性均比在成纤维细胞中高得多,而PLK1启动子是最具癌症特异性和最有希望的启动子。启动子对癌细胞的特异性从PLK1,CKS1B,POLD1,MCM2和CDC6系列下降。证实了克隆的CKS1B启动子的双向活性。它显然指导SHC1基因的表达,该基因位于人基因组中CKS1B基因的“头对头”位置。在将来使用CKS1B启动子时,应考虑此功能。克隆的启动子可用于癌症基因治疗的人工遗传构建中。

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