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缺氧诱导的肿瘤特异性启动子作为癌症基因治疗的双靶点转录调控系统

Hypoxia-inducible tumour-specific promoters as a dual-targeting transcriptional regulation system for cancer gene therapy.

作者信息

Javan Bita, Shahbazi Majid

机构信息

Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan 4934174515, Iran.

出版信息

Ecancermedicalscience. 2017 Jul 6;11:751. doi: 10.3332/ecancer.2017.751. eCollection 2017.

Abstract

Transcriptional targeting is the best approach for specific gene therapy. Hypoxia is a common feature of the tumour microenvironment. Therefore, targeting gene expression in hypoxic cells by placing transgene under the control of a hypoxia-responsive promoter can be a good strategy for cancer-specific gene therapy. The hypoxia-inducible gene expression system has been investigated more in suicide gene therapy and it can also be of great help in knocking down cancer gene therapy with siRNAs. However, this system needs to be optimised to have maximum efficacy with minimum side effects in normal tissues. The combination of tissue-/tumour-specific promoters with HRE core sequences has been found to enhance the specificity and efficacy of this system. In this review, hypoxia-inducible gene expression system as well as gene therapy strategies targeting tumour hypoxia will be discussed. This review will also focus on hypoxia-inducible tumour-specific promoters as a dual-targeting transcriptional regulation systems developed for cancer-specific gene therapy.

摘要

转录靶向是特异性基因治疗的最佳方法。缺氧是肿瘤微环境的一个常见特征。因此,通过将转基因置于缺氧反应性启动子的控制之下,在缺氧细胞中靶向基因表达可能是癌症特异性基因治疗的一个良好策略。缺氧诱导基因表达系统在自杀基因治疗中得到了更多研究,它在使用小干扰RNA(siRNA)的癌症基因敲除治疗中也可能有很大帮助。然而,该系统需要进行优化,以便在正常组织中以最小的副作用实现最大疗效。已发现组织/肿瘤特异性启动子与缺氧反应元件(HRE)核心序列的组合可增强该系统的特异性和疗效。在本综述中,将讨论缺氧诱导基因表达系统以及针对肿瘤缺氧的基因治疗策略。本综述还将重点关注作为为癌症特异性基因治疗开发的双靶向转录调控系统的缺氧诱导肿瘤特异性启动子。

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