罗卫民,罗湘玉,郭家龙,林称意,张军.miR-200b靶向VEGF抑制肺癌细胞侵袭.[J].中南医学科学杂志.,2016,(3):271-274, 289.
miR-200b靶向VEGF抑制肺癌细胞侵袭
miR-200b Promotes Non-small Cell Lung Cancer CellsInvasion by Targeting VEGF
投稿时间:2015-12-21  修订日期:2016-05-03
DOI:
中文关键词:  miR-200b  非小细胞肺癌  血管内皮生长因子  侵袭
英文关键词:MiR-200b  non-small cell lung cancer  VEGF  invasion
基金项目:湖北省教育厅科学研究计划指导性项目(B2015477). 
作者单位
罗卫民 湖北医药学院附属十堰市太和医院, 湖北 十堰 442000 
罗湘玉 湖北医药学院附属十堰市太和医院, 湖北 十堰 442000 
郭家龙 湖北医药学院附属十堰市太和医院, 湖北 十堰 442000 
林称意 湖北医药学院附属十堰市太和医院, 湖北 十堰 442000 
张军 湖北医药学院附属十堰市太和医院, 湖北 十堰 442000 
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中文摘要:
      目的 探讨miR-200b是否通过靶向调控血管内皮生长因子(VEGF)抑制人非小细胞肺癌细胞侵袭,以揭示miR-200b的抑瘤机制。方法运用qRT-PCR检测miR-200b在非小细胞肺癌和癌旁正常肺组织中的表达;将非小细胞肺癌A549细胞分为miR-200b mimics组、miR-200b inhibitors组、scramble组、VEGF-siRNA组和control-siRNA组,分别将miR-200b mimics、miR-200b inhibitors、scramble、VEGF-siRNA、control-siRNA转染于A549细胞;采用Western blot检测A549细胞中VEGF蛋白表达,采用Transwell侵袭实验分别检测A549细胞侵袭能力。结果qRT-PCR检测结果显示,miR-200b在A549、16HBE细胞的表达分别为0.704±0.053、1.582±0.071,两者比较,差异有显著性(P<0.01);Western blot结果显示,外源过表达miR-200b或沉默VEGF能明显下调A549细胞中VEGF蛋白的表达水平;Transwell侵袭实验显示,转染miR-200b mimics或沉默VEGF 36 h后穿过基底膜的细胞数分别为(127±6)和(136±8),与对照组(189±14)比较能明显抑制A549细胞的穿膜能力(P<0.05),而转染miR-200b inhibitors可拮抗VEGF-siRNA对A549细胞的侵袭抑制作用。结论miR-200b通过靶向调控VEGF抑制人非小细胞肺癌细胞侵袭。
英文摘要:
      Objective To investigate whether miR-200b promotes cell invasion of non-small cell lung cancer cells by targeting VEGF,thus to reveal molecular mechanism that miR-200b functions as a tumor suppressor in non-small cell lung cancer.MethodsThe expression of miR-200b in non-small cell lung cancer and normal lung tissues was detected by qRT-PCR.Non-small cell lung cancer cell line A549 were divided into miR-200b mimics group,miR-200b inhibitors group,scramble group,VEGF-siRNA group as well as control-siRNA group.A549 cells were transfected with miR-200b mimics,scramble,VEGF-siRNA,control-siRNA,respectively.The expressions of VEGF protein in A549 cells was detected by Western blotting.The invasion ability of A549 cells were evaluated by Transwell invasion assays.ResultsqRT-PCR showed that miR-200b was significantly down-regulated in non-small cell lung cancer tissues (0.704±0.053) than normal lung tissues (1.582±0.071).Western blot showed that the level of VEGF protein was inhibited by restored miR-200b or knock-down VEGF in A549 cells.After transfection of miR-200b mimics or knock-down VEGF for 36 h,Transwell invasion assay showed that the number of cells through the basement membrane was(127±6),(136±8),compared with the control group(189±14),it can significantly suppress the invasion of A549 cell (P<0.01).However,miR-200b inhibitors could antagonize the role of VEGF-siRNA in A549 cells.ConclusionmiR-200b suppresses cell invasion by targeting VEGF in non-small cell lung cancer.
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