文章摘要
尚荣鑫,雷 杰,段万石,葛忠虎,王孝彬,陈家宽,韩国梁.沉默BCAT1对肺癌细胞增殖、迁移及侵袭能力的影响[J].,2017,17(34):6644-6647
沉默BCAT1对肺癌细胞增殖、迁移及侵袭能力的影响
Effect of BCAT1 Knockdown on the Proliferation, Migration and Invasion of Lung Cancer Cells
投稿时间:2017-07-18  修订日期:2017-08-10
DOI:10.13241/j.cnki.pmb.2017.34.008
中文关键词: 肺癌  BCAT1  迁移  侵袭  增殖
英文关键词: Lung cancer  BCAT1  Migration  Invasion  Proliferation
基金项目:陕西省自然科学基金面上项目(2016JM8009)
作者单位E-mail
尚荣鑫 第四军医大学唐都医院胸外科 陕西 西安 710038 shangrx1978@163.com 
雷 杰 第四军医大学唐都医院胸外科 陕西 西安 710038  
段万石 第四军医大学唐都医院胸外科 陕西 西安 710038  
葛忠虎 第四军医大学唐都医院胸外科 陕西 西安 710038  
王孝彬 第四军医大学唐都医院胸外科 陕西 西安 710038  
陈家宽 第四军医大学唐都医院胸外科 陕西 西安 710038  
韩国梁 第四军医大学唐都医院胸外科 陕西 西安 710038  
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中文摘要:
      摘要 目的:研究BCAT1在肺癌细胞A549的增殖、迁移及侵袭能力中的作用。方法:通过小干扰RNA(siRNA)沉默A549细胞中BCAT1的表达,细胞分为对照组(Con)、BCAT1基因沉默组(siRNA-BCAT1)和siRNA阴性对照组(siRNA-NC)。利用Western blot检测siRNA对BCAT1的沉默效果;划痕愈合实验检测沉默BCAT1后A549细胞迁移能力的改变;Transwell小室侵袭实验检测沉默BCAT1后A549细胞侵袭能力的变化;MTT实验检测沉默BCAT1对A549细胞增殖能力的影响。结果:与Con组相比,siRNA-BCAT1组的BCAT1蛋白表达明显降低(P<0.05),细胞划痕愈合率明显降低(P<0.05),能够穿膜的细胞数明显减少(P<0.05),而Con组和siRNA-BCAT1组细胞的增殖能力比较差异无明显统计学意义(P>0.05)。结论:沉默BCAT1抑制A549细胞的迁移和侵袭能力,而对其增殖能力无影响。
英文摘要:
      ABSTRACT Objective: To investigate the effect of BCAT1 on the proliferation, migration and invasion of lung cancer A549 cells. Methods: BCAT1 was knocked down by siRNA and A549 cells were divided into three groups: control group, siRNA-BCAT1 group and siRNA-NC group. Western blot was performed to detect the expression of BCAT1. Cell migration was tested by wound healing assay and cell invasion was evaluated by Transwell assay. MTT assay was performed to investigate the effect of BCAT1 knockdown on the cell proliferation. Results: Compared with those of the control group and siRNA-NC group, the protein expression of BCAT1 in A549 cells of siRNA-BCAT1 group was significantly decreased(P<0.05), the rate of wound healing was decreased(P<0.05) and the cell invasion was suppressed(P<0.05). However, no significnat difference was found in the MTT assay results between three groups(P>0.05). Conclusion: Knockdown of the BCAT1 expression in A549 cells resulted in significant decrease of cell migration and invasion but had no impact on the proliferation of lung cancer A549 cells.
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