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曲古抑菌素A通过调控蛋白激酶C促进食管鳞癌细胞迁移
引用本文:刘丹辉,刘玉珍,陈彦民,陈智,赵宝生.曲古抑菌素A通过调控蛋白激酶C促进食管鳞癌细胞迁移[J].解剖学报,2020,51(2):228-232.
作者姓名:刘丹辉  刘玉珍  陈彦民  陈智  赵宝生
作者单位:1.新乡医学院第一附属医院胸外科; 2.新乡医学院食管癌研究所; 3.河南省神经病学研究所,河南 卫辉 453100
基金项目:新乡市科技攻关计划重点项目;河南省科技厅科技攻关计划;新乡医学院研究生科研创新支持计划
摘    要:目的探讨组蛋白去乙酰化酶抑制剂曲古抑菌素A(TSA)对人食管鳞癌细胞(ESCC)迁移能力的影响及其可能的作用机制。方法培养食管鳞癌细胞KYSE-150和EC9706;Transwell法检测TSA、蛋白激酶C(PKC)抑制剂AEB071对食管鳞癌细胞迁移的影响;观察TSA、PKC抑制剂AEB071对人食管鳞癌细胞形态学的影响;Western blotting检测E-钙黏蛋白(E-cadherin)、波形蛋白(vimentin)、β-连环蛋白(β-catenin)、Slug、ac H3和H3蛋白的表达水平。结果TSA促进食管鳞癌细胞的迁移,PKC抑制剂AEB071部分抑制TSA促进食管鳞癌细胞的迁移作用;TSA促使细胞由类椭圆形的上皮样细胞形态向类似梭形的成纤维细胞样形态的上皮-间质转化(EMT),AEB071抑制TSA诱导的细胞形态学变化;TSA处理后E-cadherin蛋白表达水平降低,vimentin、β-catenin、Slug、ac H3表达水平升高,联合应用TSA与AEB071,TSA诱导的上述EMT相关蛋白水平的变化得到部分抑制,使E-cadherin蛋白表达水平增加,vimentin、β-catenin、Slug表达水平降低。结论TSA通过促进食管鳞癌细胞EMT增加其迁移能力,其机制可能由PKC相关信号通路介导。

关 键 词:组蛋白去乙酰化酶抑制剂  曲古抑菌素A  蛋白激酶C  上皮-间质转化  食管鳞癌细胞  免疫印迹法  
收稿时间:2019-03-26
修稿时间:2019-05-13

Trichostatin A promotes the migration of esophageal squamous carcinoma cells by protein kinase C signaling pathway#br#
LIU Dan-hui LIU Yu-zhen CHEN Yan-min CHEN Zhi ZHAO Bao-sheng.Trichostatin A promotes the migration of esophageal squamous carcinoma cells by protein kinase C signaling pathway#br#[J].Acta Anatomica Sinica,2020,51(2):228-232.
Authors:LIU Dan-hui LIU Yu-zhen CHEN Yan-min CHEN Zhi ZHAO Bao-sheng
Institution:1. Department of Thoracic Surgery, the First Affiliated Hospital of Xinxiang Medical University; 2.Esophageal Cancer Institute of Xinxiang Medical University; 3.He’nan Neurology Institute at the First Affiliated Hospital of Xinxiang Medical University, He’nan Weihui 453100, China
Abstract:Objective To investigate the effect of histone deacetylase inhibitor trichostatin A (TSA) on the migration of human esophageal squamous carcinoma cells(ESCC) and the possible mechanism.Methods KYSE-150 cells and EC9706 cells were cultured and Transwell assay was performed to detect the role of TSA alone and combined with protein kinase C (PKC) inhibitor AEB071 on cell migration; the images of morphology after cells treatment with TSA or combination of AEB071 with TSA; Western blotting was conducted to examine the protein level of epithelial-mesenchymal transition (EMT) related signaling molecules.Results TSA promoted the migration of ESCC cells significantly, and PKC inhibitor AEB071 partly inhibited the effect of TSA-promoted ESCC cells migration. Treatment with TSA resulted in the cell morphology transitioned from epithelia oval-like to mesenchymal spindle-like, indicating the EMT. AEB071 partially rescued ESCC cells morphological changes which TSA induced. Western blotting showed that TSA reduced the expression of E-cadherin and augmented the expression of vimentin, β-catenin, Slug and acH3, whereas AEB071 obviously blocked the EMT-related protein level changes which induced by TSA.Conclusion TSA promotes ESCC cells migration via inducing EMT process and the mechanism may be mediated by PKC signaling pathway.
Keywords:Histone deacetylase inhibitor  Trichostatin A  Protein kinase C  Epithelial-mesenchymal transition  Esophageal squamous carcinoma cells  Western blotting  Human
  
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