Center for Ultrasound Molecular Imaging and Therapeutics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Cancer Res. 2012 Dec 1;72(23):6191-9. doi: 10.1158/0008-5472.CAN-11-4079. Epub 2012 Sep 25.
Microbubble contrast agents can specifically deliver nucleic acids to target tissues when exposed to ultrasound treatment parameters that mediate microbubble destruction. In this study, we evaluated whether microbubbles and ultrasound-targeted microbubble destruction (UTMD) could be used to enhance delivery of EGF receptor (EGFR)-directed siRNA to murine squamous cell carcinomas. Custom-designed microbubbles efficiently bound siRNA and mediated RNAse protection. UTMD-mediated delivery of microbubbles loaded with EGFR-directed siRNA to murine squamous carcinoma cells in vitro reduced EGFR expression and EGF-dependent growth, relative to delivery of control siRNA. Similarly, serial UTMD-mediated delivery of EGFR siRNA to squamous cell carcinoma in vivo decreased EGFR expression and increased tumor doubling time, relative to controls receiving EGFR siRNA-loaded microbubbles but not ultrasound or control siRNA-loaded microbubbles and UTMD. Taken together, our results offer a preclinical proof-of-concept for customized microbubbles and UTMD to deliver gene-targeted siRNA for cancer therapy.
微泡造影剂在超声处理参数介导微泡破坏时,可以特异性地将核酸递送至靶向组织。在这项研究中,我们评估了微泡和超声靶向微泡破坏(UTMD)是否可用于增强表皮生长因子受体(EGFR)靶向 siRNA 向小鼠鳞状细胞癌的递呈。定制的微泡可有效地结合 siRNA 并介导 RNA 酶保护。与递送对照 siRNA 相比,UTMD 介导的将负载 EGFR 靶向 siRNA 的微泡递送至体外培养的小鼠鳞状癌细胞可降低 EGFR 表达和 EGF 依赖性生长。同样,体内连续 UTMD 介导的 EGFR siRNA 递送至鳞状细胞癌可降低 EGFR 表达并增加肿瘤倍增时间,与接受负载 EGFR siRNA 的微泡但未接受超声或负载对照 siRNA 的微泡和 UTMD 的对照组相比。综上所述,我们的结果为使用定制微泡和 UTMD 递呈基因靶向 siRNA 进行癌症治疗提供了临床前概念验证。