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HPV18E6基因沉默对宫颈癌Hela细胞生长和凋亡的影响
引用本文:上官文学,杨业鹏,周梅,李五岭.HPV18E6基因沉默对宫颈癌Hela细胞生长和凋亡的影响[J].现代肿瘤医学,2008,16(10).
作者姓名:上官文学  杨业鹏  周梅  李五岭
作者单位:北京大学基础医学院放射医学教研室,北京,100083
摘    要:目的:观察RNA干扰法沉默HPV18E6基因表达对宫颈癌Hela细胞牛长和凋亡的影响,探索宫颈癌基因治疗的新途径。方法:针对HPV18E6 mRNA序列合成一对60bp的编码siRNA的DNA模板和一对60bp的非特异性对照DNA模板,构建pSUPER—siRNA和pSUPER—com重组质粒,瞬时转染Hela细胞;采用RT—PCR法检测质粒转染后细胞HPV18E6基因表达的变化,用蛋白免疫印迹法检测转染后Hela细胞p53、p21、Bcl-2和Bax蛋白表达变化,以细胞计数法检测细胞生长情况,Hoechest/PI双荧光活细胞染色法检测细胞凋亡。结果:pSUPER—siRNA质粒转染能有效降低HPV18E6在mRNA水平的表达,转染后48小时,抑制效率达70%以上;转染后细胞053、p21和Bax蛋白表达显著增加,Bcl-2蛋白表达减少。RNA干扰法沉默HPV18E6基因表达后,Hela细胞增殖受到明显抑制,细胞凋亡率明显增加。结论:pSUPER—siRNA质粒转染可有效抑制HPV18E6在人宫颈癌Hela细胞中的表达,抑制Hela细胞生长并促进其凋亡。以HPV18E6为靶点的RNA干扰技术可望成为宫颈癌基因治疗的新途径。

关 键 词:宫颈癌  RNA干扰  HPV18E6  凋亡

siRNA targeting of H PV18E6 inhibits the growth of Hela cells and induces apoptosis
SHANG GUAN Wen-xue,YANG Ye-peng,ZHOU Mei,LI Wu-ling.siRNA targeting of H PV18E6 inhibits the growth of Hela cells and induces apoptosis[J].Journal of Modern Oncology,2008,16(10).
Authors:SHANG GUAN Wen-xue  YANG Ye-peng  ZHOU Mei  LI Wu-ling
Abstract:Objective:To study the effects of HPV18E6-targeting siRNA on the growth and apoptosis of Hela cells and to explore a new pathway for cervical cancer genetherapy .Methods:A pair of DNA template coding siRNA against HPV18E6 and it's control template were synthesized to reconstruct pSUPER-siRNA and pSUPER -control plasmids,which was transfected transiently into Hela cells. The HPV18E6 expression in Hela cells was detected by RT-PCR. The protein expression of p53,p21, Bcl-2 and Bax was detected by Western blot.The proliferation and apoptosis of Hela cells was detected respectively by cell counting and Hoechest/PI fluorescent vital staining.Results:The siRNA expression vector against HPV18E6 mRNA was successfully constructed. The transfection of pSUPER-siRNA targeting HPV18E6 effectively decreased the expression of HPV18E6 in the Hela cells and the decrease rate was more than 70% in 48 hour after transfection.. In the Hela cells transfected with pSUPER-siRNA plasmid, the protein expression of p53,p21 and Bax was increased significantly while the expression of Bcl-2 was decreased markedly. After silence of HPV18E6 gene, the proliferation of Hela cells was obviously inhibited and the apoptotic rates were significantly increased. Conclusion: HPV18E6-targeting siRNA can significantly inhibit HPV18E6 expression, suppress the growth of Hela cells and induce apotosis. The RNA interfering technique targeting of HPV18E6 maybe can provide a new pathway for the gene therapy of cervical carcinoma..
Keywords:HPVl8E6
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