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用于癌症基因治疗的酶/前药系统

Enzyme/Prodrug Systems for Cancer Gene Therapy.

作者信息

Malekshah Obeid M, Chen Xuguang, Nomani Alireza, Sarkar Siddik, Hatefi Arash

机构信息

Department of Pharmaceutics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States.

Department of Pharmaceutics, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States; Rutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, United States.

出版信息

Curr Pharmacol Rep. 2016 Dec;2(6):299-308. doi: 10.1007/s40495-016-0073-y. Epub 2016 Oct 19.

Abstract

The use of enzyme/prodrug system has gained attention because it could help improve the efficacy and safety of conventional cancer chemotherapies. In this approach, cancer cells are first transfected with a gene that can express an enzyme with ability to convert a non-toxic prodrug into its active cytotoxic form. As a result, the activated prodrug could kill the transfected cancer cells. Despite the significant progress of different suicide gene therapy protocols in preclinical studies and early clinical trials, none has reached the clinic due to several shortcomings. These include slow prodrug-drug conversion rate, low transfection/transduction efficiency of the vectors and nonspecific toxicity/immunogenicity related to the delivery systems, plasmid DNA, enzymes and/or prodrugs. This mini review aims at providing an overview of the most widely used enzyme/prodrug systems with emphasis on reporting the results of the recent preclinical and clinical studies.

摘要

酶/前药系统的应用已受到关注,因为它有助于提高传统癌症化疗的疗效和安全性。在这种方法中,首先用一种能表达将无毒前药转化为其活性细胞毒性形式的酶的基因转染癌细胞。结果,活化的前药可杀死转染的癌细胞。尽管不同的自杀基因治疗方案在临床前研究和早期临床试验中取得了显著进展,但由于几个缺点,尚无一种进入临床。这些缺点包括前药-药物转化率低、载体的转染/转导效率低以及与递送系统、质粒DNA、酶和/或前药相关的非特异性毒性/免疫原性。本综述旨在概述最广泛使用的酶/前药系统,重点报告近期临床前和临床研究的结果。

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