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作 者:李俊[1] 王建中[2] 黄新生[2] 白广平[1] 童华[2] 周雷[2] 刘建平[2]
机构地区:[1]复旦大学附属中山医院青浦分院耳鼻咽喉科,上海201700 [2]复旦大学附属中山医院耳鼻咽喉科,上海200032
出 处:《中国耳鼻咽喉头颈外科》2013年第9期449-453,共5页Chinese Archives of Otolaryngology-Head and Neck Surgery
基 金:上海市卫生局青年基金(2009Y132);上海市青浦区科委科技发展基金(2011-19);上海市青浦区卫生局医苑新星人才培养项目(WY2011-14)联合资助
摘 要:目的通过慢病毒载体介导的RNA干扰技术,来探讨沉默miRNA-224-5p对人喉鳞状细胞癌(简称喉鳞癌)Hep-2细胞增殖、凋亡及侵袭能力的影响。方法针对目标序列合成特异性siRNA干扰片段并克隆入慢病毒载体,将重组miRNA-224-5p-RNAi-LV3转染喉鳞癌Hep-2。设为干扰组(miRNA-224-5p-siRNA,SI组)、阴性对照组(NC组)和空白对照组(BC组),分别采用聚合酶链反应方法检测miRNA-224-5p的表达情况,用CCK8法检测细胞增殖情况,流式细胞仪检测细胞周期及凋亡情况、Transwell侵袭实验检测细胞侵袭情况。结果 miRNA-224-5p-RNAi-LV3可显著降低miRNA-224-5p的表达,转染后Hep-2细胞增殖能力显著降低,细胞侵袭能力明显减弱,细胞周期及细胞凋亡均未见明显影响。结论 RNAi沉默miRNA-224-5p可以抑制Hep-2细胞增殖,并降低其侵袭能力。OBJECTIVE To explore the influence of miRNA-224-5p gene silencing on cell proliferation,apoptosis and invasion in human laryngeal cancer cell line Hep-2 by lentiviral vector-mediated RNA interference.METHODS miRNA-224-5p specific siRNA gene was synthesized and cloned into the recombinant lentiviral vector.Hep-2 cells were infected by miRNA-224-5p-siRNA recombinant lentivirus(miRNA-224-5p-siRNA-LV3).The Hep-2 cells were divided into SI group,NC group and BC group in vitro.The expression of the targets of miRNA-224-5p was detected by RT-PCR.Cell proliferation was detected by CCK8 kit.Cell cycle and apoptosis were detected by flow cytometry.The invasion was detected by Transwell test.RESULTS The expression level of miRNA-224-5p was inhibited significantly by miRNA224-5p-siRNA-LV3.The proliferation of Hep-2 was also markedly suppressed.The number of invasive cells that migrated through the chamber decreased.The cell cycle and apoptosis had no obvious effect.CONCLUSION MiRNA-224-5p gene silencing by RNAi can suppress the proliferation and reduce the invasiveness of Hep-2 cells.
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