RETRACTED: Enhanced suppression of tumor growth using a combination of NK4 plasmid DNA-PEG engrafted cationized dextran complex and ultrasound irradiation (Retracted Article)

被引:43
作者
Hosseinkhani, H
Kushibiki, T
Matsumoto, K
Nakamura, T
Tabata, Y [1 ]
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Dept Biomat, Field Tissue Engn,Sakuo Ku, Kyoto 6068507, Japan
[2] Osaka Univ, Grad Sch Med, Course Adv Med, Div Mol Regenerat Med, Osaka, Japan
关键词
ultrasound irradiation; NK4; enhanced gene expression; cationization; PEG engrafted;
D O I
10.1038/sj.cgt.7700918
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
This investigation aims to determine experimentally whether or not ultrasound (US) irradiation is effective in enhancing the in vivo gene expression of NK4 plasmid DNA and suppressing tumor growth. NK4, composed of the NH2-terminal hairpin and subsequent four-kringle domains of hepatocyte growth factor (HGF), acts as an HGF-antagonist and angiogenesis inhibitor. Dextran was cationized by introducing spermine to the hydroxyl groups to allow for polyionic complexation with NK4 plasmid DNA. The cationized dextran was additionally modified with poly( ethylene glycol) (PEG) molecules giving PEG engrafted cationized dextran. Significant suppression of tumor growth was observed when PEG engrafted cationized dextran-NK4 plasmid DNA complexes were intravenously injected into mice carrying a subcutaneous Lewis lung carcinoma tumor mass with subsequent US irradiation when compared with the cationized dextran-NK4 plasmid DNA complex and naked NK4 plasmid DNA with or without US irradiation. We conclude that complexation with PEG-engrafted cationized dextran in combination with US irradiation is a promising way to target the NK4 plasmid DNA to the tumor for gene expression.
引用
收藏
页码:479 / 489
页数:11
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