Fabrication of Polyvalent Therapeutic RNA Nanoparticles for Specific Delivery of siRNA, Ribozyme and Drugs to Targeted Cells for Cancer Therapy.

Yi Shu, Dan Shu, Zhijuan Diao, Guanxin Shen, Peixuan Guo
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引用次数: 22

Abstract

Bacteriophage phi29 DNA packaging motor is geared by a six-pRNA ring. pRNA is able to form a multimeric complex and patterned superstructures via the interaction of two reengineered interlocking loops. This unique feature makes it an ideal polyvalent vehicle for nanomachine fabrication, pathogen detection, and the delivery of therapeutics. This report describes novel approaches for the fabrication of polyvalent therapeutic pRNA nanoparticles, especially tetramers for specific siRNA delivery to cancer cells and for the silencing of targeted genes. RNA 3-D design, circular permutation, folding energy alteration, and nucleotide modification were applied to generate stable RNA nanoparticles with low toxicity. Animal trials demonstrated the high efficiency of the polyvalent RNA nanoparticles in the prevention and treatment of cancer. Using such protein-free nanoparticles as therapeutic reagents would allow for long-term administration to avoid the induction of antibody due to repeated treatment for chronic diseases.

制备多价治疗性RNA纳米颗粒,将siRNA、核酶和药物特异性递送至癌症治疗的靶细胞。
噬菌体phi29 DNA包装马达由一个6 - prna环驱动。pRNA能够通过两个重新设计的互锁环的相互作用形成多聚体复合物和图案上层结构。这种独特的特性使其成为纳米机器制造、病原体检测和治疗药物输送的理想多价载体。本报告描述了制造多价治疗性pRNA纳米颗粒的新方法,特别是用于特定siRNA递送到癌细胞和用于靶基因沉默的四聚体。采用RNA三维设计、环状排列、折叠能量改变和核苷酸修饰等方法制备稳定、低毒性的RNA纳米颗粒。动物实验证明了多价RNA纳米颗粒在预防和治疗癌症方面的高效率。使用这种无蛋白纳米颗粒作为治疗试剂将允许长期给药,以避免由于慢性疾病的重复治疗而诱导抗体。
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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