Edge Robert E, Falls Theresa J, Brown Christopher W, Lichty Brian D, Atkins Harold, Bell John C
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa Health Research Institute, Centre for Cancer Therapeutics, Ottawa, Ontario, Canada.
Mol Ther. 2008 Aug;16(8):1437-43. doi: 10.1038/mt.2008.130. Epub 2008 Jun 17.
Creation of potent oncolytic viruses (OVs) suitable for the clinic may require new strategies in virus design. Replication-competent viruses facilitate a variety of approaches to achieving tumor specificity. Altered expression of microRNAs is a common hallmark of cancer that we demonstrate can be used to alter expression of a potent wild-type viral gene to achieve tumor-specific replication of an engineered vesicular stomatitis virus (VSV). Incorporation of let-7 microRNA complementary sequences within VSV eliminates undesirable replication and associated toxicity in normal cells but permits growth in cancer cells in vitro and in vivo. This is proof of concept that viruses designed to exploit the differential microRNA expression in cancer cells is a viable approach, potentially useful in optimizing oncolytic viral gene expression for maximal antitumor activity and safety.
开发适用于临床的强效溶瘤病毒(OV)可能需要病毒设计的新策略。具有复制能力的病毒有助于实现肿瘤特异性的多种方法。微小RNA(miRNA)表达改变是癌症的常见特征,我们证明可以利用这一特征来改变强效野生型病毒基因的表达,以实现工程化水疱性口炎病毒(VSV)的肿瘤特异性复制。在VSV中掺入let-7 miRNA互补序列可消除正常细胞中不必要的复制及相关毒性,但允许其在体外和体内的癌细胞中生长。这证明了利用癌细胞中差异miRNA表达设计病毒是一种可行的方法,可能有助于优化溶瘤病毒基因表达以实现最大抗肿瘤活性和安全性。