ISSN 1004-6879

CN 13-1154/R

 

承德医学院学报 ›› 2023, Vol. 40 ›› Issue (2): 95-100.

• 基础医学 • 上一篇    下一篇

IFITM3通过P38-MAPK/EMT信号轴对胃癌细胞的影响

胡维晟1, 林嘉鑫1, 卢楠1, 黄建梅1, 李明2,*   

  1. 1.漳州卫生职业学院,福建漳州 363000;
    2.湖南医药学院
  • 收稿日期:2022-01-04 出版日期:2023-04-10 发布日期:2023-04-10
  • 通讯作者: *
  • 基金资助:
    2020年度福建省中青年教师教育科研项目(JAT201395)

Effect of IFITM3 on Gastric Cancer Cells through p38-MAPK /EMT Signaling Axis

HU Wei-sheng1, LIN Jia-xin1, LU Nan1, HUANG Jian-mei1, LI Ming2,*   

  1. 1. Zhangzhou Health Vocational College, Zhangzhou, Fujian, 363000, China;
    2. Hunan University of Medicine
  • Received:2022-01-04 Online:2023-04-10 Published:2023-04-10

摘要: 目的 探究IFITM3在胃癌中的表达及其对胃癌细胞恶性生物学行为的影响。方法 利用数据库分析IFITM3在胃癌中的表达及分析IFITM3与胃癌患者总体生存率的相关性;在胃癌细胞SGC-7901中转染si-IFITM3,利用CCK-8实验、流式细胞术和伤口愈合实验分别分析细胞增殖、凋亡及迁移。Western blot检测P38-MAPK磷酸化水平和EMT相关蛋白(E-cadherin、Snail和Vimentin)的表达。结果 IFITM3在胃癌中高表达且与胃癌患者总体生存率负相关;在SGC-7901细胞中转染si-IFITM3能有效敲低IFITM3的表达;敲低IFITM3能显著抑制细胞增殖和迁移,诱导细胞凋亡,同时也能减少P38-MAPK的磷酸化和EMT相关蛋白的表达。结论 敲低IFITM3能通过减少P38-MAPK蛋白磷酸化,抑制胃癌细胞EMT,从而减缓细胞增殖和迁移,诱导细胞凋亡。

关键词: 胃癌, IFITM3, P38-MAPK, 上皮-间质转化, 增殖

Abstract: Objective To investigate the expression of IFITM3 in gastric cancer and its effect on malignant biological behavior of gastric cancer cells. Methods The expression of IFITM3 in gastric cancer was analyzed by database and the correlation between IFITM3 and overall survival rate of gastric cancer patients was analyzed. Si-ifitm3 was transfected into GASTRIC cancer cells SGC-7901, and cell proliferation, apoptosis and migration were analyzed by CCK-8 assay, flow cytometry and wound healing assay. The phosphorylation of P38-MAPK and the expression of EMT-related proteins (e-cadherin, Snail and Vimentin) were detected by Western blot. Results IFITM3 was highly expressed in gastric cancer and negatively correlated with the overall survival rate of gastric cancer patients. Transfection of SI-IFITM3 in SGC-7901 cells could effectively knock down the expression of IFITM3. Knocking down IFITM3 can significantly inhibit cell proliferation and migration, induce cell apoptosis, and also reduce the phosphorylation of P38-MAPK and the expression of EMT-related proteins. Conclusion Knockdown IFITM3 can inhibit EMT of gastric cancer cells by reducing phosphorylation of P38-MAPK protein, thus slowing down cell proliferation and migration, and inducing cell apoptosis.

Key words: gastric cancer, IFITM3, P38-MAPK, epithelial-mesenchymal transformation, proliferation

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