刘勇刚, 黄俊勇, 梁基韵, 李曦, 罗美华. TGF-β1通过调控脂肪酸合酶促进胃癌细胞的迁移及侵袭[J]. 中国肿瘤临床, 2020, 47(13): 649-654. DOI: 10.3969/j.issn.1000-8179.2020.13.239
引用本文: 刘勇刚, 黄俊勇, 梁基韵, 李曦, 罗美华. TGF-β1通过调控脂肪酸合酶促进胃癌细胞的迁移及侵袭[J]. 中国肿瘤临床, 2020, 47(13): 649-654. DOI: 10.3969/j.issn.1000-8179.2020.13.239
Liu Yonggang, Huang Junyong, Liang Jiyun, Li Xi, Luo Meihua. TGF-β1 promotes migration and invasion of gastric cancer cells by regulating fatty acid synthase[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(13): 649-654. DOI: 10.3969/j.issn.1000-8179.2020.13.239
Citation: Liu Yonggang, Huang Junyong, Liang Jiyun, Li Xi, Luo Meihua. TGF-β1 promotes migration and invasion of gastric cancer cells by regulating fatty acid synthase[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(13): 649-654. DOI: 10.3969/j.issn.1000-8179.2020.13.239

TGF-β1通过调控脂肪酸合酶促进胃癌细胞的迁移及侵袭

TGF-β1 promotes migration and invasion of gastric cancer cells by regulating fatty acid synthase

  • 摘要:
      目的:  探讨TGF-β1通过调控脂肪酸合酶对胃癌细胞迁移及侵袭的影响。
      方法:  收集南方医科大学顺德医院2016年1月至2018年12月存档的胃癌手术切除的石蜡标本54例,采用免疫组织化学法检测人胃癌组织中转化生长因子β1(transforminggrowth factor β1,TGF-β1)及脂肪酸合成酶(fatty acid synthetase,FASN)的表达情况,分析两者之间的相关性。构建TGF-β1基因过表达及siRNA沉默载体转染胃癌细胞株,用Real-time PCR和Western blot法分别检测对FASN mRNA及蛋白表达的影响。利用siRNA行FASN做基因沉默后,采用划痕及Transwell实验检测对胃癌细胞迁移及侵袭能力的影响。
      结果:  免疫组织化学结果显示,TGF-β1与FASN在胃癌组织中的表达呈显著正相关。转染TGF-β1过表达质粒能明显上调FASN mRNA及蛋白的表达水平。反之,TGF-β1 siRNA则明显抑制FASN的表达。共转染FASN siRNA后,能减弱TGF-β1引起的N-cadherin蛋白表达、增强E-cadherin蛋白表达;划痕及Transwell实验显示能明显减弱TGF-β1所上调的细胞迁移及侵袭能力。
      结论:   FASN在TGF-β1调控的胃癌细胞的迁移及侵袭过程中发挥重要作用。

     

    Abstract:
      Objective:   To investigate the effect of TGF-β1 on the migration and invasion of gastric cancer cells, by regulating fatty acid synthetase.
      Methods:   From January 2016 to December 2018, 54 paraffin samples were collected from Shunde Hospital of Southern Medical University. Immunohistochemistry was used to detect the expression of transforming growth factor β1 (TGF-β1) and fatty acid synthetase (FASN) in human gastric cancer tissues, and the correlation between them was analyzed. Transient transfection of TGF-β1 and TGF-β1 siRNA was used to construct gastric cancer cell lines. Real-time PCR was used to detect FASN mRNA level, and Western blot was performed to examine FASN protein level. Transient transfection of FASN siRNA was used to construct gastric cancer cell lines. Wound healing assays and Transwell assays were performed to observe the effect of migration and invasion ability of gastric cancer cells. Results: Immunohistochemical results indicated that the expression of TGF-β1 and FASN in gastric cancer tissue was significantly positively correlated. TGF-β1 overexpression plasmid transfection significantly up-regulated the expression level of FASN mRNA and protein, whereas TGF-β1 siRNA significantly inhibited the expression of FASN. After co-transfection with FASN siRNA, TGF-β 1-induced N- cadherin protein expression was reduced and E- cadherin protein expression was enhenced. Scratch and Transwell experiments showed that the increased cell migration and invasion by TGF-β1 were significantly decreased.
      Conclusions:   FASN plays an important role in the migration and invasion of gastric cancer cells regulated by TGF-β1.

     

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