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Snail Down-Regulation using siRNA Complexes Delivered through Collagen Scaffolds

机译:使用通过胶原蛋白支架递送的siRNA复合物,蜗牛下调。

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Control of gene expression via small interferingRNA (siRNA) has enormous potential for the treatmentof a variety of diseases, including cancer andHuntington’s disease [1]. However, before anytherapies can be developed, effective techniques forcontrolled delivery of siRNA must be devised. In thisproof-of-concept study, siRNA was complexed with apolymer and loaded into a biomaterial scaffold. Thescaffold was introduced primarily to control the releaseof the complexes, while the polymer improved thetransfection efficiency. An optimal dose andcomplexation ratio was selected, for which more than50% down-regulation of the target gene Snail-1 (Sna1)was observed in 2D culture. Significantsustaineddown-regulation of Sna1 was observed with thescaffold system after both 2 and 7 days. Thus, thereappears to be support for further studies with othertherapeutic genes and longer time periods.
机译:通过小干扰控制基因表达 RNA(siRNA)具有巨大的治疗潜力 多种疾病,包括癌症和 亨廷顿舞蹈病[1]。但是,在任何之前 可以开发出有效的治疗方法 必须设计出可控的siRNA递送方式。在这个 概念验证研究中,将siRNA与 聚合物并装入生物材料支架中。这 引入脚手架主要是为了控制释放 配合物,而聚合物改善了 转染效率。最佳剂量和 选择了络合比,对于 目标基因Snail-1(Sna1)下调50% 在二维文化中被观察到。重大 持续 观察到Sna1的下调 支架系统在第2天和第7天后均可使用。因此, 似乎为其他人的进一步研究提供了支持 治疗基因和更长的时间。

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