Non-viral gene carrier mediated short hairpin RNA interference for inhibition of tumor cells growth

被引:2
|
作者
Duan YaJun [1 ]
Yang CuiHong [1 ]
Zhang ZhenFang [1 ]
Liu JianFeng [1 ]
Zheng JunNian [2 ]
Xu Yong [3 ]
Kong DeLing [1 ]
Yu YaoTing [1 ]
机构
[1] Nankai Univ, Key Lab Bioact Mat, Minist Educ, Coll Life Sci, Tianjin 300071, Peoples R China
[2] Xuzhou Med Coll, Lab Urol, Affiliated Hosp, Xuzhou 221002, Peoples R China
[3] Tianjin Med Univ, Dept Urol, Hosp 2, Tianjin Inst Urol, Tianjin 300211, Peoples R China
来源
CHINESE SCIENCE BULLETIN | 2009年 / 54卷 / 17期
基金
中国国家自然科学基金; 国家杰出青年科学基金;
关键词
nucleostemin; nonviral gene vectors; gene therapy; RNA interference; targeted gene therapy; EXPRESSION; CANCER; SUPPRESSION; SYSTEM;
D O I
10.1007/s11434-009-0316-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A tumor-targeting gene vector G250mAb-PEI-PEG has been prepared by modification of polyethylenimine (PEI) with polyethyleneglycol (PEG) and G250, a monoclonal antibody against the G250 antigen on tumor cell surface. The transfection efficiency was as high as 70% in G250 positive HeLa cells, whereas the transfection efficiency was relatively low (30%) in normal NIH3T3 cells. A plasmid encoding the short hairpin RNA (shRNA) specific for nucleostemin gene (NS) was efficiently transfected into the HeLa cells with this nonviral gene vector. RNA interference down-regulated the expression of NS gene in HeLa cells, inhibited cells proliferation and induced apoptosis. However, the growth and activity of the NIH3T3 cells were not affected under the same treatment. These results indicate that the reported nonviral gene vector, G250mAb-PEI-PEG, can target and efficiently deliver genes into HeLa cells, and has the potential for the cervical cancer treatment.
引用
收藏
页码:2947 / 2952
页数:6
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