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微小RNA miR-199a/a^*模拟物转染肝癌细胞HepG2中Met原癌基因的表达
引用本文:张烈民. 微小RNA miR-199a/a^*模拟物转染肝癌细胞HepG2中Met原癌基因的表达[J]. 胃肠病学和肝病学杂志, 2009, 18(8): 714-716
作者姓名:张烈民
作者单位:湖北省妇幼保健院内科,湖北,武汉,430070
摘    要:目的探讨在肝癌细胞系HepG2中,Met是否为miR-199a/a^*的靶基因。方法将miR-199a/a^*的模拟物及阴性对照物分别转染至HepG2细胞中,转染后48h及72h分别提取RNA及蛋白行RT—PCR及Western Blot检测Met的表达。结果与阴性对照相比,转染Up-miR-199a^*组的MetmRNA(P〈0.05)和蛋白(P〈0.001)表达水平均显著下调;而Up—miR-199a组与阴性对照组相比无统计学差异。结论肝癌细胞HepG2中miR-199a^*负调控Met的mRNA及蛋白表达。

关 键 词:微小RNA  miR-199a/a^*  Met  肝癌  HepG2细胞系

The expression of oncogene Met in the miR-199a/a* mimic transfected HepG2 cell line
ZHANG Liemin. The expression of oncogene Met in the miR-199a/a* mimic transfected HepG2 cell line[J]. Chinese Journal of Gastroenterology and Hepatology, 2009, 18(8): 714-716
Authors:ZHANG Liemin
Affiliation:ZHANG Liemin( Department of Internal Medicine, Hubei Women and Children' s Hospital, Wuhan 430070, China)
Abstract:Objective To explore Met gene is the target of miR-199a/a^* or not in the hepatocellular carcinoma cell line HepG2. Methods The simulant of miR-199a/a^* or the negative control (NC) were transfected into HepG2 cells. Total RNA was isolated from transfected cells at 48 hours post-transfection and protein at 72 hours. Then Met expression was detected by RT-PCR and Western Blot. Results Compared with NC group, the expressions of Met mRNA (P 〈 0.05 ) and protein (P 〈0. 001 ) were obviously down-regulated in Up-miR-199a^* group. However, there was no significant difference between Up-miR-199a and NC groups. Conclusion In HepG2 cell line, miR-199a^* negatively regulate Met expression both in mRNA and protein level.
Keywords:miR-199a/a*  Met
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