Systemic Delivery of Tumor Suppressor microRNA Mimics Using a Neutral Lipid Emulsion Inhibits Lung Tumors in Mice

被引:531
作者
Trang, Phong [2 ,3 ]
Wiggins, Jason F. [1 ]
Daige, Christopher L. [1 ]
Cho, Chris [3 ]
Omotola, Michael [1 ]
Brown, David [1 ]
Weidhaas, Joanne B. [3 ]
Bader, Andreas G. [1 ]
Slack, Frank J. [2 ]
机构
[1] Mirna Therapeut Inc, Austin, TX 78744 USA
[2] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Therapeut Radiol, New Haven, CT 06510 USA
关键词
CELLULAR SENESCENCE; GENE-THERAPY; IN-VIVO; CANCER; P53; MIR-34A; REPRESSES; CELLS; SIRT1; EXPRESSION;
D O I
10.1038/mt.2011.48
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
MicroRNAs (miRNAs) are emerging as potential cancer therapeutics, but effective delivery mechanisms to tumor sites are a roadblock to utility. Here we show that systemically delivered, synthetic miRNA mimics in complex with a novel neutral lipid emulsion are preferentially targeted to lung tumors and show therapeutic benefit in mouse models of lung cancer. Therapeutic delivery was demonstrated using mimics of the tumor suppressors, microRNA-34a (miR-34a) and let-7, both of which are often down regulated or lost in lung cancer. Systemic treatment of a Kras-activated autochthonous mouse model of non-small cell lung cancer (NSCLC) led to a significant decrease in tumor burden. Specifically, mice treated with miR-34a displayed a 60% reduction in tumor area compared to mice treated with a miRNA control. Similar results were obtained with the let-7 mimic. These findings provide direct evidence that synthetic miRNA mimics can be systemically delivered to the mammalian lung and support the promise of miRNAs as a future targeted therapy for lung cancer.
引用
收藏
页码:1116 / 1122
页数:7
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