Different strategies of gene delivery for treatment of cancer and other disorders

Elnaz Agi, Z. Mosaferi, Sepideh Khatamsaz, P. Cheraghi, Nooshin Samadian, A. Bolhassani
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引用次数: 5

Abstract

Gene therapy is the gene transfer into host cells for treatment of acquired and genetic disorders. For this purpose, there are awide variety of gene delivery methods with special properties including viral and non-viral vectors. The non-viral methods usephysical forces or chemical compounds (natural or synthetic) to transfer DNA into a cell. The efficiency of the non-viral genetherapy depends on conquering four different intra- and extra-cellular barriers such as cellular uptake, endosomal escape, nuclearentry, and gene expression. Among various gene carriers, some viral vectors such as Adenovirus, Lentivirus, Vaccinia as well asgene gun and lipofection achieved to clinical trials. In this mini-review, we briefly describe different approaches for gene deliveryand their applications in various phases of clinical trials.
基因传递治疗癌症和其他疾病的不同策略
基因治疗是将基因转移到宿主细胞中治疗获得性和遗传性疾病。为此,有多种具有特殊性质的基因传递方法,包括病毒载体和非病毒载体。非病毒方法利用物理力量或化合物(天然的或合成的)将DNA转移到细胞中。非病毒基因治疗的有效性取决于克服四种不同的细胞内和细胞外障碍,如细胞摄取、内体逃逸、核分裂和基因表达。在多种基因载体中,腺病毒、慢病毒、牛痘等病毒载体以及基因枪和脂肪感染等已进入临床试验阶段。在这篇综述中,我们简要介绍了基因传递的不同方法及其在临床试验不同阶段的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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