Conditionally replicating adenoviruses expressing short hairpin RNAs silence the expression of a target gene in cancer cells

被引:54
作者
Carette, JE [1 ]
Overmeer, RM
Schagen, FHE
Alemany, R
Barski, OA
Gerritsen, WR
van Beusechem, VW
机构
[1] VU Univ, Ctr Med, Dept Med Oncol, Div Gene Therapy, NL-1081 HV Amsterdam, Netherlands
[2] Inst Catala Oncol, Translat Res Lab, Barcelona, Spain
[3] Baylor Coll Med, Dept Pediat, Mol Diabet & Metab Sect, Harry B & Aileen Gordon Diabet Res Lab, Houston, TX 77030 USA
关键词
D O I
10.1158/0008-5472.CAN-03-3530
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RNA interference (RNAi) is a posttranscriptional silencing mechanism triggered by double-stranded RNA that was recently shown to function in mammalian cells. Expression of cancer-associated genes was knocked down by expressing short hairpin RNAs (shRNAs) in cancer cells. By virtue of its excellent target specificity, RNAi may be used as a new therapeutic modality for cancer. The success of this approach will largely depend on efficient delivery of shRNAs to tumor cells. Tumor-selective replication competent viruses are especially suited to efficiently deliver anticancer genes to tumors. In addition, their intrinsic capacity to kill cancer cells makes these viruses promising anticancer agents per se. In this study, conditionally replicating adenoviruses were constructed encoding shRNAs targeted against firefly luciferase. These replicating viruses were shown to specifically silence the expression of the target gene in human cancer cells down to 30% relative to control virus. This finding offers the promise of using RNAi in the context of cancer gene therapy with oncolytic viruses.
引用
收藏
页码:2663 / 2667
页数:5
相关论文
共 28 条
[1]   Oligonucleotide-based knockdown technologies: Antisense versus RNA interference [J].
Achenbach, TV ;
Brunner, B ;
Heermeier, K .
CHEMBIOCHEM, 2003, 4 (10) :928-935
[2]   Characterization of the human aldehyde reductase gene and promoter [J].
Barski, OA ;
Cabbay, KH ;
Bohren, KM .
GENOMICS, 1999, 60 (02) :188-198
[3]   Human aldehyde reductase promoter allows simultaneous expression of two genes in opposite directions [J].
Barski, OA ;
Siller-Lopez, FS ;
Bohren, KM ;
Gabbay, KH ;
Aguilar-Cordova, E .
BIOTECHNIQUES, 2004, 36 (03) :382-+
[4]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[5]   Innovation - New tools for functional mammalian cancer genetics [J].
Brummelkamp, TR ;
Bernards, R .
NATURE REVIEWS CANCER, 2003, 3 (10) :781-789
[6]   Efficient generation of recombinant adenovirus vectors by homologous recombination in Escherichia coli [J].
Chartier, C ;
Degryse, E ;
Gantzer, M ;
Dieterle, A ;
Pavirani, A ;
Mehtali, M .
JOURNAL OF VIROLOGY, 1996, 70 (07) :4805-4810
[7]   RNA interference is a functional pathway with therapeutic potential in human myeloid leukemia cell lines [J].
Cioca, DP ;
Aoki, Y ;
Kiyosawa, K .
CANCER GENE THERAPY, 2003, 10 (02) :125-133
[8]  
DeWeese TL, 2001, CANCER RES, V61, P7464
[9]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[10]   Consortium uses RNAi to uncover genes' function [J].
Frankish, H .
LANCET, 2003, 361 (9357) :584-584