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Transcriptional targeting of small interfering RNAs into cancer cells
被引:20
作者:
Huynh, Trang
Walchli, Seastien
Sioud, Mouldy
[1
]
机构:
[1] Univ Oslo, Dept Immunol, Norwegian Radium Hosp, Univ Dept,Mol Med Grp, N-310 Oslo, Norway
[2] Univ Oslo, Dept Biochem, Norwegian Radium Hosp, Univ Dept, N-310 Oslo, Norway
关键词:
RNA interference;
hairpin RNAs;
transcriptional regulation;
gene therapy;
survivin promoter;
tissue-specific promoter;
small interfering RNAs;
D O I:
10.1016/j.bbrc.2006.09.127
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Small interfering RNAs (siRNAs) are widely used for analyzing gene function and have the potential to be developed into human therapeutics. However, persistent siRNA expression in normal cells may cause toxic side effects. Therefore, the therapeutic applications of RNAi in cancer require either the specific delivery of synthetic siRNAs into cancer cells or the control of siRNA expression. Accordingly, we have developed a cancer-specific vector that expresses siRNAs from the human survivin promoter. A plasmid vector expressing siRNAs under this promoter enabled efficient gene silencing of gene expression in different cancer cell lines. The levels of inhibition were comparable to that obtained with the constitutively active U6 promoter. By contrast to U6 promoter, no significant gene silencing was obtained with the Survivin promoter in normal mammary epithelial cells. Collectively, these data indicate that the survivin promoter is suitable for directing siRNA expression in cancer cells, but not normal cells. (c) 2006 Elsevier Inc. All rights reserved.
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页码:854 / 859
页数:6
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