Antisense RNA of Survivin Gene Inhibits the Proliferation of Leukemia Cells and Sensitizes Leukemia Cell Line to Taxol-induced Apoptosis
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李文涵
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王晓娟
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雷萍
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Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
雷萍
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叶庆
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Department of Pathobiology and Physiology, Medicine and Life Science College of Jianghan UniversityDepartment of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
叶庆
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朱慧芬
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张悦
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邵静芳
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Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
邵静芳
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杨敬
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Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
杨敬
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沈关心
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Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
沈关心
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[1] Department of Immunology, School of Basic Medical Sciences, Tongji Medical College, Huazhong University of Science and Technology
[2] Department of Pathobiology and Physiology, Medicine and Life Science College of Jianghan University
The effects of survivin antisense RNA on proliferation of leukemia cell line HL-60 and taxol-induced chemotherapy was explored. A cDNA fragment of survivin obtained by RT-PCR was inserted into a plamid vector named pcDNA3 in the reverse direction. The vector encoding antisense RNA of survivin was confirmed by restriction enzyme digestion and DNA sequencing. The recombi-nant plasmid was delivered into HL-60 cells by electroporation. Growth curves were plotted based on cell counting. Trypan blue dye exclusion assay and MTT assay were carried out after the cells were incubated with taxol. DNA gel electrophoresis and nuclear staining were performed for cell apoptosis assay. The correct construction of the recombinant plasmid has been identified by restriction enzyme digestion and DNA sequencing. A stable down-regulation has been achieved in HL-60 SVVas cells after G418 selection. Compared to HL-60 cells, the proliferation of HL-60 SVVas cells was signifi-cantly inhibited (P<0.05). Cytotoxicity assays indicated that IC50 of HL-60 SVVas for taxol was rela-tively lower than controls (P<0.01). Apoptosis assays revealed that taxol-induced apoptosis was de-tected in HL-60 SVVas cells incubated with 50 ng/ml taxol for 12 h, while in HL-60 cells incubated with 100 ng/ml taxol for 72 h. It was suggested that Survivin antisense RNA could inhibit the prolif-eration of HL-60 cells and enhance taxol-induced apoptosis in HL-60 cells, which may lay an ex-perimental foundation for further research on gene therapy in leukemia.
[5]
Survivin: anti-apoptosis protein and a prognostic marker for tumor progression and recurrence. Sela B. Handchirurgie Mikrochirurgie Plastische Chirurgie . 2002
[5]
Survivin: anti-apoptosis protein and a prognostic marker for tumor progression and recurrence. Sela B. Handchirurgie Mikrochirurgie Plastische Chirurgie . 2002