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用于通过全身给药在肿瘤中实现高效基因沉默的刺激响应性小干扰RNA载体。

Stimuli-responsive siRNA carriers for efficient gene silencing in tumors via systemic delivery.

作者信息

Shim Min Suk, Chang Seong-Sil, Kwon Young Jik

机构信息

Division of Bioengineering, Incheon National University, Incheon 406-772, Republic of Korea.

出版信息

Biomater Sci. 2014 Jan 29;2(1):35-40. doi: 10.1039/c3bm60187k. Epub 2013 Oct 24.

Abstract

Development of efficient carriers for small interfering RNA (siRNA) delivery and validation tools for assessing in vivo RNA interference (RNAi) efficiency is crucial to advance RNAi-based therapeutics to the clinic. Here, acid-degradable ketalized linear polyethylenimine (KL-PEI) designed for efficient, stimuli-responsive, and biocompatible siRNA delivery was used to complex with GFP-silencing siRNA (GFP siRNA) for in vivo RNAi. The in vivo gene silencing efficiency of GFP siRNA/KL-PEI polyplexes was evaluated at mRNA, protein, and histological levels using a mouse bearing a GFP-expressing tumor. Intravenously injected GFP siRNA/KL-PEI polyplexes significantly reduced GFP expression in tumors and whole blood of mice, depending on the dosage of GFP siRNA and the time course. Average GFP mRNA levels in the tumors of siRNA/KL-PEI polyplex-injected mice were also reduced. The described siRNA carriers and RNAi validation methodologies in this study may provide insightful clues for the development of RNAi-based therapeutics and preclinical trials.

摘要

开发用于小干扰RNA(siRNA)递送的高效载体以及用于评估体内RNA干扰(RNAi)效率的验证工具,对于将基于RNAi的疗法推进到临床至关重要。在此,设计用于高效、刺激响应和生物相容性siRNA递送的酸可降解酮化线性聚乙烯亚胺(KL-PEI)与用于体内RNAi的绿色荧光蛋白(GFP)沉默siRNA(GFP siRNA)复合。使用携带表达GFP肿瘤的小鼠,在mRNA、蛋白质和组织学水平评估GFP siRNA/KL-PEI多聚体的体内基因沉默效率。静脉注射的GFP siRNA/KL-PEI多聚体显著降低了小鼠肿瘤和全血中的GFP表达,这取决于GFP siRNA的剂量和时间进程。注射siRNA/KL-PEI多聚体的小鼠肿瘤中的平均GFP mRNA水平也降低了。本研究中描述的siRNA载体和RNAi验证方法可能为基于RNAi的疗法开发和临床前试验提供有见地的线索。

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