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作 者:易世江[1] 陈柏林[1] 申一鸣[1] 陈莹[1] 刘鹏[1] 雷迅[1]
机构地区:[1]桂林医学院附属医院耳鼻咽喉头颈外科,541001
出 处:《实用医学杂志》2016年第21期3517-3520,共4页The Journal of Practical Medicine
基 金:广西桂林市科技局科技攻关项目(编号:20140505-3);广西教育厅课题(编号:200911MS168)
摘 要:目的:探讨沉默叉头框C1(forkhead boxC1,FOXC1)基因对鼻咽癌细胞系5-8F凋亡和细胞周期的影响。方法:利用si RNA技术在5-8F细胞中沉默FOXC1基因,通过流式细胞仪检测细胞凋亡和周期的变化,应用Western blot方法检测相关蛋白Bcl-2、CyclinD1的表达。结果:FOXC1基因沉默后5-8F细胞的凋亡率明显增高,且Bcl-2蛋白表达减弱(P<0.05),处于G1期的细胞数减少,处于S期的细胞数增多,同时降低了CyclinD1蛋白的表达(P<0.05)。结论:沉默FOXC1基因可能通过下调Bcl-2表达促进5-8F细胞凋亡,又可能通过调节CyclinD1的表达影响5-8F细胞周期分布,这说明FOXC1在鼻咽癌进展中的作用值得进一步研究。Objective To explore the impacts of silenced FOXC1 gene on the apoptosis and cell cycle of NPC cell lines 5-8F. Methods siRNA was used to silence FOXC1 gene in 5-8F ceils. The apoptosis and cell cycle of 5-8F cells were then detected by flow cytometry, and the protein expressions of Bcl-2 and CyclinD1 were detected by Western blot. Results The apoptotic rate was increased significantly, the cell cycle distribution in the G1 and S phase were changed, and the protein expressions of Bcl-2 and CyclinD1 were decreased in 5-8F cells after FOXC1 was silenced (P〈0.05). Conclusions Silenced FOXC1 gene may induce the apoptosis of 5-8F cell line by regulating the expression of Bcl-2, and it may also change the cell cycle distribution of 5-8F cell line through adjusting the expression of CyclinD1, showing the role of FOXC1 in development of nasopharyngeal carcinoma is worth further researching.
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