International Journal of Clinical Research
International Journal of Clinical Research. 2022; 6: (10) ; 10.12208/j.ijcr.20220499 .
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长沙医学院 湖南长沙
*通讯作者: 熊婷,单位:长沙医学院 湖南长沙;
目的 探讨FDI-6调控叉头框转录因子 M1( FoxM1) 对人肝癌细胞增殖、侵袭的影响。方法 应用定量聚合酶链反应检测肝癌细胞HepG2中加入FDI-6后FoxM1的表达影响,细胞增殖实验和细胞迁移实验检测FoxM1下调空肝癌细胞的增殖和侵袭能力。结果 在HepG2 细胞中,FDI-6≥20μmol/L可明显下调FoxM1的表达。表达。结论 FDI-6能下调 FoxM1的表达,抑制肝癌细胞增殖,导致细胞周期发生停滞,降低细胞迁移能力。
Objective: To investigate the effects of FDI-6 regulating forkhead box transcription factor M1 (FoxM1) on the proliferation and invasion of human hepatoma cells. Methods: Quantitative polymerase chain reaction was used to detect the expression of FoxM1 in HepG2 cells after adding FDI-6. Cell proliferation and migration tests were used to detect the ability of FoxM1 to down regulate the proliferation and invasion of empty hepatoma cells. Results: In HepG2 cells, FDI-6 ≥ 20 μ Mol/L could significantly down regulate the expression of FoxM1. expression. Conclusion : FDI-6 can down regulate the expression of FoxM1, inhibit the proliferation of hepatoma cells, lead to cell cycle arrest, and reduce the ability of cell migration.
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