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作 者:余文发[1] 赵玉林[2] 王萍[3] 马慧敏[1] 张国正[1] 鲁保才[1] 董明敏[3]
机构地区:[1]新乡医学院第一附属医院耳鼻咽喉头颈外科,河南新乡453100 [2]郑州大学第一附属医院耳鼻咽喉头颈外科 [3]新乡医学院第三附属医院功能检查科
出 处:《临床耳鼻咽喉头颈外科杂志》2014年第12期894-897,共4页Journal of Clinical Otorhinolaryngology Head And Neck Surgery
基 金:河南省高等学校青年骨干教师资助计划(No:2010GGJS-120);和河南省卫生科技创新人才工程(No:2010141)联合资助
摘 要:目的:探讨siRNA沉默人喉癌Hep-2细胞C-erbB-2基因对细胞增殖的影响,及其与PI3K/Akt信号通路的关系。方法:利用siRNA技术转染Hep-2细胞C-erbB-2基因,RT-PCR3检测siRNA转染后C-erbB-2mRNA的水平变化,MTT检测细胞增殖情况改变,Western blot检测ERK1/2和AKT1蛋白磷酸化变化情况。结果:转染C-erbB-2siRNA 24h后的Hep-2细胞C-erbB-2mRNA水平出现下调,细胞增殖抑制率增加,ERK1/2和AKT1蛋白磷酸化水平也相应降低,C-erbB-2基因表达与ERK1/2和AKT1蛋白磷酸化水平之间有显著相关性。结论:siRNA沉默Hep-2细胞C-erbB-2抑制Hep-2细胞增殖,这种增殖抑制可能通过降低ERK1/2和AKT1蛋白磷酸化水平实现。Objective:To investigate the effects of short interfering RNA(siRNA) silencing C-erbB-2 gene on the proliferation of laryngeal carcinoma Hep-2 cells and to explore the relationship between C-erbB2 gene and pI3K/Akt signal pathwayl Method:C-erbB-2 siRNA was transfected to Hep-2 cells,and mRNA expression of C- erbB-2 was detected by RT-PCR. MTT was applied to detect the proliferation of Hep-2 cells. Western blot was used to detect the phosphorylation changes of protein ERK1/2 and AKT1. Result:The mRNA level of C-erbB-2 in Hep-2 cells declined obviously at 24 h after transfection of C-erbB-2 siRNA. The proliferation of transfected Hep- 2 cells was inhibited, and protein phosphorylation levels of ERK1/2 and AKT1 decreased simultaneously. The expression of C-erbB-2 gene was obviously correlated with the protein phosphorylation levels of ERK1/2 and AKT1. Couclusion:C-erbB-2 silence by siRNA can efficiently inhibit the proliferation of Hep-2 cells, which may be a- chieved by decreasing the phosphorylation level of ERK1/2 and AKT1.
关 键 词:喉肿瘤 C—erbB-2基因 ERK1 2 AKT1
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