基础医学与临床 ›› 2021, Vol. 41 ›› Issue (12): 1780-1785.

• 研究论文 • 上一篇    下一篇

FOXM1促进子宫内膜癌细胞系HEC-1B增殖、迁移和侵袭

黄博, 程苾恒, 解美婷, 刘珊汕, 魏敏*   

  1. 湖北省人民医院 妇产科, 湖北 武汉 430000
  • 收稿日期:2021-01-08 修回日期:2021-05-06 发布日期:2021-12-03
  • 通讯作者: *weimintime@sina.com

FOXM1 promotes proliferation, migration and invasion of endometrial cancer cell line HEC-1B

HUANG Bo, CHENG Bi-heng, XIE Mei-ting, LIU Shan-shan, WEI Min*   

  1. Department of Obstetrics and Gynecology, Hubei General Hospital, Wuhan 430000, China
  • Received:2021-01-08 Revised:2021-05-06 Published:2021-12-03
  • Contact: *weimintime@sina.com

摘要: 目的 探讨抑制叉头框蛋白M1(FOXM1)基因的表达对子宫内膜癌细胞增殖、迁移和侵袭的影响。方法 选择人子宫内膜癌细胞系HEC-1B,将细胞分为3组:空白对照组、阴性对照组、siRNA-FOXM1组;实时荧光定量PCR检测各组细胞FOXM1、血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)mRNA表达水平;CCK8法检测各组细胞增殖能力;细胞划痕实验检测各组细胞迁移能力;Transwell小室法检测各组细胞侵袭能力;Western blot检测各组细胞VEGF和bFGF基因的蛋白表达。结果 与HEECs细胞相比,HEC-1B细胞FOXM1 mRNA和蛋白表达显著升高(P<0.05);干扰FOXM1表达后,FOXM1 mRNA和蛋白表达、HEC-1B细胞增殖、迁移和侵袭能力与空白对照组和阴性对照组相比均显著降低(P<0.05);抑制FOXM1表达后,HEC-1B细胞VEGF、bFGF mRNA及蛋白表达显著降低(P<0.05)。结论 抑制FOXM1的表达可以抑制HEC-1B细胞增殖、迁移及侵袭能力,其机制可能与抑制VEGF、bFGF的表达有关。

关键词: 叉头框蛋白M1, 子宫内膜癌, HEC-1B细胞, 血管内皮生长因子, 碱性成纤维细胞生长因子

Abstract: Objective To explore the effect of inhibiting the expression of forkhead box protein M1 (FOXM1) gene on the proliferation, migration and invasion of endometrial cancer cell line HEC-1B. Methods Human endometrial carcinoma cell line HEC-1B was selected as the subject and divided into three groups: blank control group, negative control group and siRNA-FOXM1 group. Real-time qPCR was used to detect the expression of FOXM1, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) mRNA in cells of each group. CCK8 method was used to detect the proliferation of cells. Cell scratch test to detect the ability of cell migration in each group. Transwell chamber method was performed to detect the invasion ability of cells in each group. The protein expression of VEGF and bFGF were detected by Western blot. Results Compared with HEECs, the expression of FOXM1 mRNA and protein in HEC-1B cells was significantly increased (P<0.05). The expression of FOXM1 mRNA and protein, proliferation, migration and invasion ability of HEC-1B cells were significantly lower than those of blank control group and negative control group (P<0.05). The mRNA and protein expressions of VEGF and bFGF in hec-1b cells were significantly decreased after FOXM1 expression was inhibited (P<0.05). Conclusions Inhibiting of FOXM1 expression can inhibit the proliferation, migration and invasion of HEC-1B cells, and the mechanism might be related to inhibiting the expression of VEGF and bFGF.

Key words: forkhead box protein M1, endometrial carcinoma, HEC-1B cell, vascular endothelial growth factor, basic fibroblast growth factor

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