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Non-viral gene carrier mediated short hairpin RNA interference for inhibition of tumor cells growth 被引量:2

Non-viral gene carrier mediated short hairpin RNA interference for inhibition of tumor cells growth
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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. 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.
出处 《Chinese Science Bulletin》 SCIE EI CAS 2009年第17期2947-2952,共6页
基金 Supported by the National Natural Science Foundation of China (Grant No. 20774050) National Natural Science Funds for Distinguished Young Scholar (Grant No. 30725030) National Basic Research Program of China (Grant No. 2009CB918900-G)
关键词 短发夹RNA RNA干扰 病毒基因 肿瘤细胞 细胞生长 载体介导 NIH3T3细胞 HELA细胞 nucleostemin, nonviral gene vectors, gene therapy, RNA interference, targeted gene therapy
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