吉林大学学报(医学版) ›› 2019, Vol. 45 ›› Issue (01): 28-32.doi: 10.13481/j.1671-587x.20190106

• 基础研究 • 上一篇    

沉默线粒体核糖体蛋白L35基因对人食管癌TE-1细胞生长的影响

王爱馥, 张奇, 张道明, 修雨婷, 丁雅明, 刘林林   

  1. 吉林大学第二医院放疗科, 吉林 长春 130041
  • 收稿日期:2018-07-03 发布日期:2019-01-28
  • 通讯作者: 刘林林,教授,博士研究生导师(Tel:0431-81136261,E-mail:2660424632@qq.com) E-mail:2660424632@qq.com
  • 作者简介:王爱馥(1993-),女,吉林省敦化市人,在读医学硕士,主要从事胸部肿瘤基础和临床方面的研究。

Effect of silencing mitochondrial ribosomal protein L35 gene on growth of human esophageal cancer TE-1 cells

WANG Aifu, ZHANG Qi, ZHANG Daoming, XIU Yuting, DING Yaming, LIU Linlin   

  1. Department of Radiotherapy, Second Hospital, Jilin University, Changchun 130041, China
  • Received:2018-07-03 Published:2019-01-28
  • Contact: 国家自然科学基金资助课题(81773523) E-mail:2660424632@qq.com

摘要: 目的:探讨慢病毒介导沉默线粒体核糖体蛋白L35(MRPL35)基因对人食管癌TE-1细胞生长的影响,并阐明其机制。方法:选择3种人食管癌TE-1、ECA109和KYSE150细胞,采用实时定量PCR法检测3种细胞中MRPL35 mRNA相对表达水平。食管癌TE-1细胞分为shMRPL35组和shCtrl组,分别加入沉默靶基因带有嘌呤霉素抗性的si-RNA慢病毒和带有嘌呤霉素抗性的阴性对照si-RNA慢病毒进行感染,建立稳定沉默MRPL35基因的食管癌细胞系,实时定量PCR及Western blotting法检测各组细胞中MRPL35基因沉默效率,采用CCK-8法检测各组细胞生长曲线,Annexin Ⅴ-PE/7AAD双染色后流式细胞术检测细胞凋亡率。结果:3种食管癌细胞均表达MRPL35基因,3种细胞中MRPL35 mRNA表达水平比较差异无统计学意义(P>0.05)。实时定量PCR法和Western blotting法检测,shMRPL35组TE-1细胞中MRPL35 mRNA和蛋白表达水平明显低于shCtrl组(P<0.05)。与shCtrl组比较,shMRPL35组TE-1细胞生长速度明显降低(P<0.05),凋亡率明显升高(P<0.01)。结论:沉默MRPL35基因可抑制食管癌细胞TE-1增殖,并通过凋亡途径发挥作用。

关键词: 线粒体核糖体蛋白L35, 食管癌TE-1细胞, 细胞凋亡

Abstract: Objective: To investigate the effect of lentivirus-mediated silencing of mitochondrial ribosomal protein L35 (MRPL35) gene on the growth of human esophageal cancer TE-1 cells,and to clarify its mechanism.Methods: Three kinds of human esophageal cancer cells, TE-1, ECA109 and KYSE150, were selected. The relative expression levels of MRPL35 mRNA in three kinds of cells by real-time quantitative PCR. The esophageal cancer TE-1 cells were divided into shMRPL35 group and shCtrl group,and the cells were infected with si-RNA lentivirus and si-RNA lentivirus; the esophageal cancer cell line stably silenting the MRPL35 gene was established. Real-time quantitative PCR and Western blotting methods were used to detect the efficiency of MRPL35 gene silencing.The cell growth curves in various groups were detected by CCK-8 method, and the apoptotic rates were detected by flow cytometry after Annexin Ⅴ-PE/7AAD double staining.Results: Three kinds of esophageal cancer cells expressed MRPL35 gene, and the expression levels were not statistically significant between them(P>0.05). The results of real-time quantitative PCR and Western blotting methods showed that the mRNA and protein levels of MRPL35 in the TE-1 cells in shMRPL35 group were significantly lower than those in shCtrl group(P<0.05). Compared with shCtrl group, the cell growth speed in shMRPL35 group was decreased (P<0.05), and the apoptotic rate was significantly increased (P<0.01).Conclusion: Silencing MRPL35 gene can inhibit the proliferation of esophageal cancer TE-1cells and plays a role through the apoptotic pathway.

Key words: mitochondrial ribosomal protein L35, esophageal cancer TE-1 cells, apoptosis

中图分类号: 

  • R735.1