文章摘要
温伟伟,李洪波,姜英健,秦凯强,梁忆波,马 雷,郑红梅,张佃良.Sprouty-2对胃癌细胞上皮间质转化及侵袭转移的影响[J].,2017,17(17):3250-3254
Sprouty-2对胃癌细胞上皮间质转化及侵袭转移的影响
Effect of Sprouty-2 on the Epithelial-mesenchymal Transition, Migration and Invasion of Human Gastric Cancer
投稿时间:2017-01-08  修订日期:2017-02-02
DOI:10.13241/j.cnki.pmb.2017.17.012
中文关键词: 胃癌  Sprouty-2  上皮-间质转化  侵袭  转移
英文关键词: Stomach Neoplasms  Sprouty-2  Epithelial-mesenchymal transition  Invasion  Migration
基金项目:国家自然科学基金项目(81270448,81470890)
作者单位E-mail
温伟伟 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011 wenwewe@hotmail.com 
李洪波 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
姜英健 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
秦凯强 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
梁忆波 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
马 雷 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
郑红梅 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
张佃良 青岛大学 青岛市市立医院结直肠中心 山东 青岛 266011  
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中文摘要:
      摘要 目的:研究Sprouty2(SPRY2)基因在胃癌肿瘤细胞上皮间质转化(EMT)和侵袭转移的影响。方法:体外培养人胃癌细胞(BGC-823),采用慢病毒介导的shRNA沉默SPRY2基因,并用实时定量PCR与Western blot检测其SPRY2、E-钙黏蛋白(E-cadherin)、波形蛋白(vimentin)的表达,采用细胞划痕实验、Transwell实验检测SPRY2基因沉默后的胃癌细胞侵袭转移能力变化。结果:在慢病毒介导shRNA沉默SPRY2基因的人胃癌BGC-823细胞中,SPRY2的mRNA和蛋白表达明显降低(P<0.05),SPRY2沉默后人胃癌细胞E-cadherin的蛋白表达增多(P<0.05),vimentin的蛋白表达减少(P<0.05)。此外,SPRY2沉默后,胃癌细胞迁移能力和侵袭能力明显减弱(P值均P<0.05)。结论:Sprouty-2基因通过调节E-cadherin与vimentin的表达参与胃癌细胞的上皮-间质转化,进而促进胃癌细胞的迁移与侵袭。
英文摘要:
      ABSTRACT Objective: To investigate the effect of suppressed Sprouty2 (SPRY2) on the epithelial-mesenchymal transition (EMT), migration and invasion of human gastric cancer. Methods: Human gastric cancer line (BGC-823) was transfected with shRNA-SPRY2 mediated by recombinant lentivirus to establish a cell line (shRNA- SPRY2- BGC-823) which was stably suppressed to express SPRY2. The expression level of SPRY2, EMT-related marker proteins (E-cadherin and vimentin) were examined using real-time PCR and West- ern blot in human BGC-823 cells. In addition, migration and invasion assays were performed to assess the effect of SPRY2 on the BGC-823 cells using Matrigel-coated plate, transwell membrane chamber, and wound healing models, respectively. Results: The human gastric cancer line (shRNA- SPRY2- BGC-823) was successfully constructed by lentivirus stable transfection to suppress the expression levels of SPRY2. The expression of SPRY2 was significantly decreased after knockdown of SPRY2 in BGC-823 cells compared with control-shRNA and non-transfection. The results from real-time PCR and Western blot indicated that the mRNA and protein expression of the epithelial cell marker E-cadherin was significantly increased, and the mesenchymal cell markers vimentin was significantly de- creased after knockdown of SPRY2 in BGC-823 cells. Moreover, after SPRY2 knockdown, abilities of migration and invasion were sig- nificantly attenuated in shRNA- SPRY2- BGC-823 cells. Conclusion: SPRY2 knockdown significantly promote the EMT by regulating the expressions of E-cadherin and vimentin, which further enhanced the migration and invasion of human gastric cancer in vitro.
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