检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:朱学锋[1] 李德春[2] 陈益君[1] 许建伟[1] 顾继礼[1] 朱东明[2] 岑建农
机构地区:[1]泰兴市人民医院肝胆外科,225400 [2]苏州大学附属第一医院普通外科 [3]江苏省血液研究所
出 处:《江苏医药》2010年第16期1924-1927,共4页Jiangsu Medical Journal
基 金:卫生部科学研究基金(WKJ2004-2-011)
摘 要:目的观察RNAi体外沉默基质金属蛋白酶2(MMP-2)基因对胰腺癌PANC-1细胞MMP-2mRNA表达的抑制作用。方法设计靶向MMP-2的siRNA,并构建到pGCsi-U6质粒,重组质粒脂质体法转染PANC-1细胞;流式细胞术检测细胞GFP表达率,RQ-PCR检测细胞MMP-2的mRNA表达水平。结果 PCR鉴定证实重组质粒构建成功,质粒转染细胞GFP表达率最高达82.1%。转染干扰质粒的PANC-1细胞MMP-2基因mRNA表达抑制了71.74%(P<0.05)。结论 RNAi明显抑制胰腺癌PANC-1细胞MMP-2mRNA的表达,可望RNAi能为胰腺癌治疗开辟新的思路。Objective To investigate the inhibitory effects of RNA interference(RNAi) on the expression of matrix metalloproteinase-2 (MMP-2) mRNA of human pancreatic carcinoma cell line PANC-1 in vitro.Methods Small interference RNA(siRNA) targeting MMP-2 gene was designed and constructed to plasmid pGCsi-U6.Recombinant plasmids were transfected to pancreatic carcinoma cell line PANC-1 cells with lipofectamine.Green fluorescence protein(GFP) was evaluated by flow cytometry after transfection.RQ-PCR was used to detect the expression of MMP-2 mRNA.ResultsPCR confirmed that the MMP-2 siRNA plasmid was successfully constructed.The best efficiency of GFP after transfection was 82.1% in PANC-1 cells.After transfected by the MMP-2 siRNA plasmid,the MMP-2 mRNA expression of PANC-1 cells was suppressed by 71.74%(P0.05).ConclusionRNAi targeting MMP-2 gene can obviously suppress the expression of MMP-2 mRNA of PANC-1 cells.RNAi is expected to open up a new approach to pancreatic carcinoma therapy.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.145