Hickerson Robyn P, Vlassov Alexander V, Wang Qian, Leake Devin, Ilves Heini, Gonzalez-Gonzalez Emilio, Contag Christopher H, Johnston Brian H, Kaspar Roger L
TransDerm Inc., Santa Cruz, California, USA.
Oligonucleotides. 2008 Dec;18(4):345-54. doi: 10.1089/oli.2008.0149.
RNA interference offers enormous potential to develop therapeutic agents for a variety of diseases. To assess the stability of siRNAs under conditions relevant to clinical use with particular emphasis on topical delivery considerations, a study of three different unmodified siRNAs was performed. The results indicate that neither repeated freeze/thaw cycles, extended incubations (over 1 year at 21 degrees C), nor shorter incubations at high temperatures (up to 95 degrees C) have any effect on siRNA integrity as measured by nondenaturing polyacrylamide gel electrophoresis and functional activity assays. Degradation was also not observed following exposure to hair or skin at 37 degrees C. However, incubation in fetal bovine or human sera at 37 degrees C led to degradation and loss of activity. Therefore, siRNA in the bloodstream is likely inactivated, thereby limiting systemic exposure. Interestingly, partial degradation (observed by gel electrophoresis) did not always correlate with loss of activity, suggesting that partially degraded siRNAs retain full functional activity. To demonstrate the functional activity of unmodified siRNA, EGFP-specific inhibitors were injected into footpads and shown to inhibit preexisting EGFP expression in a transgenic reporter mouse model. Taken together, these data indicate that unmodified siRNAs are viable therapeutic candidates.
RNA干扰为开发针对多种疾病的治疗药物提供了巨大潜力。为了评估在与临床应用相关的条件下,尤其是在局部给药考虑因素下,小干扰RNA(siRNA)的稳定性,我们对三种不同的未修饰siRNA进行了研究。结果表明,无论是反复冻融循环、长时间孵育(21摄氏度下超过1年),还是在高温下较短时间孵育(高达95摄氏度),通过非变性聚丙烯酰胺凝胶电泳和功能活性测定法测量,均对siRNA的完整性没有任何影响。在37摄氏度下暴露于毛发或皮肤后也未观察到降解。然而,在37摄氏度下于胎牛血清或人血清中孵育会导致降解和活性丧失。因此,血液中的siRNA可能会失活,从而限制全身暴露。有趣的是,(通过凝胶电泳观察到的)部分降解并不总是与活性丧失相关,这表明部分降解的siRNA保留了全部功能活性。为了证明未修饰siRNA的功能活性,将增强绿色荧光蛋白(EGFP)特异性抑制剂注射到脚垫中,并在转基因报告小鼠模型中显示可抑制预先存在的EGFP表达。综上所述,这些数据表明未修饰的siRNA是可行的治疗候选物。