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Vector-based RNAi, a novel tool for isoform-specific knock-down of VEGF and anti-angiogenesis gene therapy of cancer
被引:88
|作者:
Zhang, L
Yang, N
Mohamed-Hadley, A
Rubin, SC
Coukos, G
[1
]
机构:
[1] Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[2] Dept Obstet & Gynecol, Div Gynecol Oncol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Cell & Mol Biol Program, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Med, Ctr Res Reprod & Womens Hlth, Philadelphia, PA 19104 USA
关键词:
RNA interference;
VEGF;
isoform;
angiogenesis;
gene therapy;
ovarian cancer;
D O I:
10.1016/S0006-291X(03)00495-9
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:
Vascular endothelial growth factor (VEGF) carries out multifaceted functions in tumor development, and it exists as at least five isoforms with distinct biologic activities and clinical implications. Several strategies have been developed to block VEGF for cancer therapy; however, the approach to target-specific VEGF isoform(s) has not been explored to date. In the present study, we show that DNA vector-based RNA interference (RNAi), in which RNAi sequences targeting murine VEGF isoforms are inserted downstream of an RNA polymerase III promoter, has potential applications in isoform-specific "knock-down" of VEGF. Large molecular weight VEGF isoforms were specifically reduced in vitro in the presence of isoform-specific RNAi constructs. Additionally, HI promoter may be superior to U6 promoter when used for vector-based RNAi of VEGF isoforms. This strategy provides a novel tool to study the function of various VEGF isoforms and may contribute to VEGF isoform-specific treatment in cancer. (C) 2003 Elsevier Science (USA). All rights reserved.
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页码:1169 / 1178
页数:10
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