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作 者:刘习强[1] 黄洪章[1] 潘朝斌[1] 王方金[2] 张彬[1] 梁蔚文[3]
机构地区:[1]中山大学附属第二医院口腔颌面外科 [2]中山大学达安基因诊断中心 [3]林百欣医学实验中心
出 处:《中华口腔医学杂志》2006年第7期403-406,共4页Chinese Journal of Stomatology
基 金:国家自然科学基金资助项目(30271423;30471896)
摘 要:目的探讨靶向小干扰RNA表达框架(SEC)对舌癌细胞内源性人端粒酶逆转录酶基因(hTERT)的特异性抑制作用。方法利用两步法PCR技术构建多条SEC,采用第5代聚酰胺-胺型树枝状高聚物(G5 PAMAM-D)纳米微球介导SEC转染Tca8113细胞,应用实时荧光定量RT-PCR技术和Western-blot等检测内源性hTERT的表达水平,并进一步筛选出最有效的小干扰RNA靶序列。结果针对不同靶位点设计的SEC干扰效果有显著差异,SEC-A的干扰效果最强,并且能以高度序列特异性方式沉默hTERT基因的表达;此外,转染次数与载体理化特性亦可影响SEC的干扰效应(P<0.05)。结论RNA干扰效应主要取决于靶序列;G5 PAMAM-D纳米载体能够介导SEC-A高效抑制内源性hTERT基因的表达;hTERT基因有望成为舌癌基因治疗的理想靶点。Objective To determine whether the human telomerase reverse transcriptase (hTERT) gene silencing could be effectively induced by PCR-derived siRNA expression cassettes (SEC) transfected by the fifth generation polyamidoamine dendrimer (G5 PAMAM-D) in Tca8113 cells. Methods Four SEC were rationally designed and constructed based on a two-step PCR reaction. The SEC were then transferred into TcaS113 cells using G5 PAMAM-D, and hTERT expression was investigated by real-time fluorescence-quantitative reverse transcriptase-PCR and western blot analysis. Results The RNA interference effects of the SEC targeted for varying hTERT mRNA positions showed a significant disparity. Among them, SEC-A revealed the most potent inhibitory effects (above 95% of reduction), followed by SEC-D and SEC-C, and SEC-B had no effect on hTERT expression (P 〉 0. 05 ). That the endogenous hTERT gene silencing induced by G5 PAMAM dendrimer-mediated SEC-A was highly sequence-specific, and multiple transfection as well as properties of the vectors were routinely attributable to the specific suppression. Conclusions Specific inhibition of endogenous hTERT expression by use of a PCR-based short hairpin siRNA technique and dendrimer transfer system may serve as a novel strategy for treatment of tongue cancers expressing hTERT in vitro.
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