首页 | 本学科首页   官方微博 | 高级检索  
检索        

TRAP1 通过TGF / Smad3 通路对膀胱癌的迁移和侵袭能力的影响
引用本文:王,哲,张,敬,陈怀安,张,潮,张晓云,刘,硕,苗文隆,李凤歧.TRAP1 通过TGF / Smad3 通路对膀胱癌的迁移和侵袭能力的影响[J].中国免疫学杂志,2017,33(9):1306.
作者姓名:        陈怀安      张晓云      苗文隆  李凤歧
摘    要:目的:探讨TRAP1蛋白对膀胱癌细胞迁移和侵袭的影响及机制。方法:采用Western blot从膀胱癌细胞株中挑选出高表达TRAP1的细胞系BIU-87;使用TRAP1沉默慢病毒(LV3-TRAP1)沉默TRAP1,使用GFP荧光及PCR检测LV3-TRAP1沉默效率;Transwell和划痕实验分别检测沉默TRAP1蛋白表达后对膀胱癌细胞侵袭和迁移能力的影响;CM-H2DCFDA荧光染色细胞检测膀胱癌细胞内活性氧水平;Western blot检测相关信号通路TGF/Smad3蛋白的表达情况。结果:LV3-TRAP1慢病毒可以有效地抑制TRAP1蛋白的表达;沉默TRAP1蛋白的表达可以有效抑制膀胱癌细胞的侵袭和迁移能力、降低膀胱癌细胞内活性氧水平;同时TGF/Smad3信号通路中的TGF、Smad2及Smad3蛋白表达也相应降低。结论:沉默TRAP1蛋白可以通过调控TGF/Smad3信号通路来抑制膀胱癌细胞的侵袭和迁移能力。

关 键 词:TRAP1  膀胱癌  TGF  Smad3  ROS  

Effect of TRAP1 on invasion and migration of human bladder cancer through TGF/Smad3 signal pathway
Abstract:Objective:To investigate the effect and related mechanism of TRAP1 on the invasion and migration of human bladder cancer through TGF/Smad3 signal path.Methods: Selected from BIU-87 of high expression of TRAP1 in bladder cancer cell lines through Western blot techniques.TRAP1 knockdown lentivirus (LV3-TRAP1) was used to silence the expression of TRAP1.GFP fluorescene and PCR detector was used to detected the efficiency of gene silencing and the effectiveness of gene silencing;effect of TRAP1 on the invasion and migration ability of BIU-87 were detected by Transwell matrigel invasion assays and wound healing assays,CM-H2DCFDA fluorescent staining was used to deteced the cell ROS of BIU-87 with LV3-TRAP1.Detected the level of TGF/Smad3 signal protein by Western blot.Results: LV3-TRAP1 lentivirus could effectively inhibit the expression of TRAP1 compared with LV3-NC.LV3-TRAP1 lentivirus could effectively inhibit the cell RPS of BIU-87.Knockdown the expression of TRAP1 could inhibit the invasion and migration of BIU-87.Knockdown the expression of TRAP1 in BIU-87 could reduce the protein level of TGF/Smad3.Conclusion: Silencing TRAP1 could inhibit the invasion and migration of bladder cancer cell through TGF/Smad3 signal pathway.
Keywords:
本文献已被 CNKI 等数据库收录!
点击此处可从《中国免疫学杂志》浏览原始摘要信息
点击此处可从《中国免疫学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号