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作 者:蒋明东[1] 彭志平[1] 尹晓玲[1] 李少林[1] 仝蜀生[2] 鄢勇[2] 王正洪[2]
机构地区:[1]重庆医科大学核医学教研室,重庆400016 [2]重庆市第九人民医院肿瘤放疗中心,重庆400700
出 处:《中国癌症杂志》2006年第10期805-808,共4页China Oncology
基 金:国家自然科学基金资助(No:30370422和30570523)
摘 要:背景与目的:胃癌是全人类常见恶性肿瘤之一。在我国,胃癌居各种癌症死亡之首,其总体五年生存率仅15%~20%。在目前尚无有效一级预防措施的情况下,积极探讨有效防治胃癌的方法成为必然趋势。本研究利用RNA干扰稳定筛选-抑制技术,抑制人端粒酶逆转录酶(hTERT)基因表达,探讨靶向hTERT基因RNAi对胃癌细胞增殖的抑制效应。方法:设计靶向hTERT基因的小干扰RNA,构建重组表达质粒pGenesil—shRNA—hTERT并导入人胃癌细胞系SGC7901细胞株,经G418筛选,建立稳定表达siRNA—hTERT的细胞株。采用real time RT—PCR、MTT和PCR—TRAP法同时检测pGenesil-shRNA—hTERT稳定抑制组和未处理SGC7901细胞组hTERT基因表达、端粒酶活性及细胞增殖变化。结果:在稳定表达pGenesil—shRNA—hTERT的SGC7901细胞株中,RNAi效力持续、稳定存在,hTERT mRNA表达、端粒酶活性明显降低,瘤细胞增殖被抑制。结论:RNA干扰能持续、稳定地抑制靶基因hTERT mRNA表达及肿瘤细胞增殖,是潜在的肿瘤基因治疗新方法。Background and purpose: Stomach cancer is one of the most common malignancy of human being. In our country, it is one of leading cancer death, 5-yr survival rate for the patients is just 15%-20%. At present, we do not have effective first line prevent measure for the disease, it becomes more and more important to pursue a effective method to prevent and treat gastric cancer . In our in vitro study, the inhibition of gastric-carcinoma cell SGC7901 proliferation by RNA interference could be observed. Methods: The stable screenlng-inhibition technique of RNAi was adopted to stably inhibit the expression of hTERT. Small hairpin interfering RNA (shRNA) targeting hTERT gene was designed, recombinant plasmid pGenesil-shRNA-hTERT was constructed, and the plasmid was transfected into gastric-carcinoma SGC7901 cells that clones were selected by G418 in order to establish gastric-carcinoma cell lines with stable expression of pGenesil-shRNA-hTERT. Real-time RT-PCR, MTF and PCR-TRAP were utilized to detect the alterations of hTERT mRNA expressions, telomerase activity and cell proliferation. Results: The effectiveness of RNAi could be observed in gastric-carcinoma SGC7901 cells with stable expression of pGenesil-shRNA-hTERT, in these cell lines, the expression of hTERT mRNA was obviously down-regulated. Meanwhile, the telomerase activity was significantly decreased, gastric-carcinoma SGC7901 cell proliferation was significantly inhibited in pGenesil-shRNA-hTERT group compared to negative control group. Conclusions: RNAi may continually and stably suppress hTERT mRNA expression and cell proliferation, which is a potential new approach for gene therapy of neoplasm.
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