生物技术通报 ›› 2024, Vol. 40 ›› Issue (4): 287-296.doi: 10.13560/j.cnki.biotech.bull.1985.2023-0935

• 研究报告 • 上一篇    下一篇

连翘叶茶对肝癌细胞增殖和迁移功能的影响及其作用机制

滕文龙(), 吴永娜, 王德富, 牛颜冰()   

  1. 山西农业大学生命科学学院,晋中 030600
  • 收稿日期:2023-10-06 出版日期:2024-04-26 发布日期:2024-04-30
  • 通讯作者: 牛颜冰,女,博士,教授,研究方向:药用植物遗传学;E-mail: niuyanbingbest@163.com
  • 作者简介:滕文龙,男,硕士,研究方向:药用植物遗传学;E-mail: 1294171341@qq.com
  • 基金资助:
    山西省自然科学基金项目(202203021212471)

Effect of Forsythia suspensa Leaves Tea on HCC Proliferation and Migration Function and Its Mechanism of Action

TENG Wen-long(), WU Yong-na, WANG De-fu, NIU Yan-bing()   

  1. College of Life Sciences, Shanxi Agricultural University, Jinzhong 030600
  • Received:2023-10-06 Published:2024-04-26 Online:2024-04-30

摘要:

目的】探究连翘叶茶粗提物及其主要成分连翘苷和连翘酯苷A对肝癌细胞LM3增殖和迁移功能的影响及其作用机制。【方法】利用水提法提取连翘叶绿茶和红茶,HPLC方法检测连翘绿茶和连翘红茶中有效成分连翘苷、连翘酯苷A的含量。采用CCK8实验,探究两种连翘叶茶粗提物、连翘苷和连翘酯苷A对肝癌细胞LM3增殖的影响;利用两种连翘叶茶粗提物、连翘苷和连翘酯苷A培养肝癌细胞LM3,通过细胞划痕实验,观察24、48、72、96 h细胞迁移情况,检测两种连翘叶茶粗提物、连翘苷和连翘酯苷A对肝癌细胞LM3迁移的影响;使用RT-PCR技术,检测增殖迁移相关基因Ki-67ErkPI3KmTOR的表达,揭示连翘叶茶粗提物及其主要成分连翘苷和连翘酯苷A影响肝癌细胞增殖迁移功能的分子机制。【结果】连翘叶绿茶和红茶粗提物、连翘苷均显著抑制肝癌细胞LM3的增殖和迁移,连翘酯苷A显著抑制肝癌细胞LM3的迁移。其中,连翘绿茶粗提物在低、中和高浓度,培养时间24、48、72 h,均可明显抑制肝癌细胞增殖和迁移。连翘红茶粗提物随着浓度升高对LM3细胞增殖和迁移的抑制效果不断增强,在高浓度72 h抑制效果最佳。RT-PCR结果分析,其主要作用机制可能是通过降低Ki-67基因表达量来实现的。【结论】连翘叶绿茶和连翘叶红茶粗提物及连翘苷和连翘酯苷A均能够通过降低Ki-67表达抑制肝癌细胞LM3的增殖或迁移。

关键词: 连翘叶茶, 连翘苷, 连翘酯苷A, 肝癌细胞, CCK-8, 划痕实验, Ki-67

Abstract:

Objective】This work aims to investigate the effects and mechanisms of crude extract of F. suspensa leaves tea and its main components, phillyrin and Forsythia glycoside A, on the proliferation and migration function of hepatocellular carcinoma LM3. 【Method】 Water extraction method was used to extract green tea and black tea from Forsythia suspensa leaves tea, HPLC was used to detect the content of effective components such as phillyrin and Forsythia glycoside A in F. suspensa green tea and F. suspensa black tea. CCK8 experiment was used to explore the effects of crude extracts of two types of F. suspensa leaves tea, phillyrin and Forsythia glycoside A on the proliferation of hepatocellular carcinoma LM3. Two crude extracts of Forsythia suspensa leaves tea, phillyrin and Forsythia glycoside A, were used to culture hepatocellular carcinoma LM3. The migration of cells was observed at 24, 48, 72, and 96 h, and the effects of the two crude extracts of F. suspensa leaves tea, phillyrin and Forsythia glycoside A on the migration of hepatocellular carcinoma LM3 were detected through the cell scratch test. To reveal the molecular mechanism of crude extract of F. suspensa leaves tea and its main components phillyrin and Forsythia glycoside A affect the proliferation and migration of hepatocellular carcinoma. The expressions of proliferation and migration-related gene Ki-67, Erk, PI3K and mTOR were detected using RT-PCR technology.【Result】Both the green tea and black tea extracts of F. suspensa leaves tea, as well as phillyrin and Forsythia glycoside A, significantly inhibited the proliferation and migration of hepatocellular carcinoma LM3, while Forsythia glycoside A significantly inhibited the migration of hepatocellular carcinoma line LM3. Among them, the crude extract of F. suspensa green tea significantly inhibited the proliferation and migration of HCC at low, medium, and high concentrations when 24, 48, and 72 h. The inhibitory effect of the crude extract of F. suspensa black tea on the proliferation and migration of LM3 cells continued to increase with increasing concentration, and the best inhibitory effect was achieved at high concentration for 72 h. The analysis of RT-PCR results suggests that its main mechanism of action may be achieved by reducing the expression levels of proliferation and migration related genes such as Ki-67.【Conclusion】In summary, the crude extracts of F. suspensa green tea and F. suspensa black tea, as well as phillyrin and Forsythia glycoside A, can inhibit the proliferation or migration of HCC LM3 by reducing the expression of Ki-67.

Key words: Forsythia suspensa leaves tea, phillyrin, Forsythia glycoside A, hepatocellular carcinoma, CCK-8, scratch experiment, Ki-67