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作 者:郭涛[1] 顾春东[1] 舒鑫[1] 郑勋[1] 赵士磊[1] 李锦绣
机构地区:[1]大连医科大学附属第一医院肺癌诊疗基地胸外科,116011 [2]大连市肺癌组织基因库工程实验室
出 处:《中华实验外科杂志》2014年第11期2480-2482,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81173453);大连市科技计划重大项目(2012E15SF141)
摘 要:目的 构建稳定沉默Y盒结合蛋白1(YB-1)基因的人肺腺癌A549细胞株并观察其增殖能力.方法 以脂质体将两种沉默YB-1基因的shRNA真核表达载体转染人肺腺癌细胞株A549,G418筛选稳定转染细胞株.逆转录-聚合酶链反应(RT-PCR)、实时荧光定量聚合酶链反应(FQ-PCR)及Westem blot法检测YB-1基因表达;噻唑蓝(MTT)法绘制细胞生长曲线.结果 稳定转染细胞株稳定表达绿色荧光蛋白(GFP);RT-PCR、FQ-PCR和Western blot法检测结果显示稳定转染组细胞株A549-746与A549-326 YB-1 mRNA和蛋白表达(0.41±0.01与0.39±0.06、0.43±0.10与0.20±0.24、0.49 ±0.06与0.24±0.02)较对照组明显下降(P<0.05);噻唑蓝(MTT)检测稳定转染组较对照组生长速度降低(P<0.05).结论 成功建立稳定表达GFP,并稳定沉默YB-1基因的人肺腺癌细胞株A549-746和A549-326,沉默YB-1可抑制A549细胞增殖能力.Objective To establish a human lung adenocarcinoma A549 cell line with RNA interference for YB-1 gene silencing which can stably express green fluorescent protein (GFP) and to observe the effects of silencing Y-box binding protein (YB-1) gene on proliferation in lung adenocarcinoma A549 cells.Methods The human lung adenocarcinoma A549 cells were transfected with shRNA plasmid specific for the YB-1 gene,and were then selected through G418.G418-resistant clones were generated and screened using reverse transcription polymerase chain reaction (RT-PCR),real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) and Western blotting analysis.Cell proliferation was examined by methyl thiazolyl tetrazolium.Results The G418-resistant clones (A549-746 and A549-326) showed much lower level of YB-1 mRNA (0.41 ± 0.01 and 0.39 ± 0.06) than A549-shNC (P 〈 0.05) under RT-PCR.A549-746 and A549-326 cell clones showed much lower level of YB-1 mRNA (0.43 ±0.10 and 0.20 ± 0.24) and protein expression (0.49 ± 0.06 and 0.24 ± 0.02) than A549-shNC (P 〈 0.05) under FQ-PCR and Western blotting analysis.Meanwhile,the G418-resistan clones (A549-746 and A549-326) stably expressed GFP in vitro.The cell growth rate in YBX1-homo-746 and YBX1-homo-326 groups was decreased significantly at the first 24 h (P 〈 0.05).Conclusion The lung cancer cell lines A549-746 and A549-326 with stable YB-1 gene silencing and GFP expression were successfully established,and silencing YB-1 gene could inhibit the proliferation of lung adenocarcinoma A549 cells.
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