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微小RNA脱靶溶瘤微小核糖核酸病毒的插入稳定性及体内测试

Insert Stability and In Vivo Testing of MicroRNA-Detargeted Oncolytic Picornaviruses.

作者信息

Schulze Autumn J

机构信息

Department of Molecular Medicine, Mayo Clinic College of Medicine, Rochester, MN, USA.

出版信息

Methods Mol Biol. 2020;2058:77-94. doi: 10.1007/978-1-4939-9794-7_5.

Abstract

Although a variety of oncolytic viruses under clinical investigation have proven to be safe, the overall efficacy of oncolytic viruses as monotherapies has been suboptimal. While responses to combination therapies are much more promising, the development of oncolytic virus monotherapies with enhanced potency is imperative. With this initiative comes the need for improved mechanisms of virus targeting to prevent off-target toxicities. MicroRNA-detargeting has emerged as an invaluable tool for preventing unwanted toxicities of oncolytic viruses, particularly for picornaviruses. Here we describe methods to test the genetic stability of microRNA response elements in vitro and to evaluate the detargeting efficiency and therapeutic index of a microRNA-detargeted picornavirus in vivo. Although the methods described herein are specific to picornaviruses, microRNA-detargeting and these assays can be adapted for different classes of oncolytic viruses.

摘要

尽管多种正在临床研究的溶瘤病毒已被证明是安全的,但溶瘤病毒作为单一疗法的总体疗效并不理想。虽然联合疗法的反应更有前景,但开发具有更强效力的溶瘤病毒单一疗法势在必行。随着这一举措的实施,需要改进病毒靶向机制以防止脱靶毒性。微小RNA去靶向已成为预防溶瘤病毒不必要毒性的宝贵工具,尤其是对于微小核糖核酸病毒。在这里,我们描述了在体外测试微小RNA反应元件遗传稳定性以及在体内评估微小RNA去靶向微小核糖核酸病毒的去靶向效率和治疗指数的方法。尽管本文所述方法特定于微小核糖核酸病毒,但微小RNA去靶向和这些测定可适用于不同类别的溶瘤病毒。

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