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机构地区:[1]山东省千佛山医院检验科,山东济南250014 [2]山东省肿瘤医院基础研究中心,山东济南250117 [3]山东大学医学院生物化学与分子生物学研究所,山东济南250012
出 处:《中华肿瘤防治杂志》2007年第16期1215-1219,共5页Chinese Journal of Cancer Prevention and Treatment
基 金:山东省科技厅科技攻关项目(032050111)
摘 要:目的:探讨鸟氨酸脱羧酶(ODC)基因作为宫颈癌治疗靶基因的可行性。方法:采用慢病毒介导的RNA干扰技术,沉默Hela细胞ODC基因,建立ODC稳定沉默的细胞系Hela/ODC,用定量RT-PCR和免疫印迹检测ODC的表达水平。用MTT实验、克隆形成实验、细胞倍增时间和细胞周期分析评价ODC基因沉默对Hela细胞生长的影响。结果:Hela/ODC的ODC mRNA和蛋白质表达水平均明显下降,mRNA水平下调93.4%。Hela/ODC的增殖受到明显抑制,细胞倍增时间从22.3h延长到32.0h,细胞周期分析S期细胞增加,G0/G1期和G2/M期细胞显著减少。结论:慢病毒载体介导RNA干扰能够稳定沉默ODC基因表达,从而成功抑制肿瘤细胞的生长,表明以ODC基因为靶基因进行宫颈癌的基因治疗是可行的。OBJECTIVE: To verify the feasibility of using ornithine decarboxylase (ODC) as a target gene in cervical cancer therapy. METHODS: A lentiviral system harboring both enhanced green fluorescent protein reporter gene and the ODC short hairpin RNA expression cassette was constructed. Then the stable ODC gene silencing cell lines Hela/ODC were established. Real-time RT-PCR analysis of mRNA and Western blot analysis of proteins were used to evaluate the expression of ODC gene. The growth-inhibiting characteristics were identified by MTT, clone formation, doubling time and cell cycle analysis, respectively. RESULTS: In the cells studied, ODC mRNA level in Hela/ODC was 93.4% decrease of that in Hela, the reduction of ODC mRNA and protein with lentiviral vectors was significant and specific. Proliferation of Hela/ODC cells was obviously retarded. The cells grew much slower with a delayed population doubling time for about 10 h (from 22.3 h to 32.0 h) in vitro. The ability of single-cell colony growth was also signif- icantly inhibited in ODC-down-regulated cells. Moreover, the proportion of Hela/ODC cells in S phase was increased and the proportions in G0/G1 phase and G2/M phase were both decreased of cell cycle. CONCLUSIONS: Lentiviral vector is capable of down-regulating ODC, resulting in impressive anticancer effects. It offers a powerful new strategy for cancer gene therapy and may be useful in the control of cervical cancer.
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