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机构地区:[1]福建医科大学附属第一医院肝胆胰外科,福州350005
出 处:《中华实验外科杂志》2014年第1期20-22,共3页Chinese Journal of Experimental Surgery
摘 要:目的 观察微小RNA(miR)-10b对人胰腺癌细胞AsPC-1细胞(以下简称AsPC-1)表达RhoC蛋白的影响.方法 以脂质体转染法将重组正、反义真核表达载体pPG-CMV-增强绿色荧光蛋白(EGFP)-miR-10b转染AsPC-1细胞株(分为正、反义组),实时荧光定量聚合酶链反应(FQ-PCR)和荧光显微镜检测载体瞬时表达的效率,Matrigel实验评价不同组间细胞迁移侵袭能力的差异;Western blot检测细胞RhoC蛋白的表达.结果 转染正义组miR-10b表达量增加10倍,反义组减少至对照组的14%.差异均有统计学意义(P<0.05).细胞RhoC蛋白的表达水平:正义组为(95.7±8.5)像素单位;反义组为(28.5±5.7)像素单位,差异均有统计学意义(P<0.05);细胞移行实验:正义组移行细胞数为(85±7)个,反义组为(32±5)个,差异有统计学意义(P<0.05);细胞侵袭实验:正义组细胞穿膜细胞数为(35±9)个,反义组为(8±3)个,差异有统计学意义(P<0.05).结论 miR-10b可促进胰腺癌细胞RhoC蛋白的表达,并影响胰腺癌细胞侵袭迁移的能力.Objective To observe the effect of microRNA (miR)-10b on the expression of RhoC in human pancreatic cancer cell line AsPC-1.Methods The recombinant eukaryotic expression plasmid vector with miR-10b sequence [pPG-CMV-enhanced green fluorescent protein (EGFP)-miR-10b] or the antisense sequence was transfected into human pancreatic cancer cell line (AsPC-1) with lipofectamine,and the efficiency of the instant expression was confirmed by real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) and fluorescence microscope.The difference of the migration and invasion of the cells was evaluated by matrigel assay,and the expression of RhoC was evaluated by Western blotting.Results The expression of miR-10b in the sense group was increased by 10 folds,and in antisense group,the expression was decreased to 14% compare to the control (P 〈 0.05).The expression of RhoC protein in the sense group was (95.7 ± 8.5) unit,and that in the antisense group (28.5 ± 5.7) unit (P 〈0.05).As compared to the antisense group,the number of migrating and penerating cells was decreased from (85 ±7) and (35 ±9) to (32±5) and (8 ±3) in the sense group (P〈0.05) Conclusion miR10b can up-regulate the expression of RhoC,and promote the migration and invasion of the AsPC-1 cells.
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