摘要
【目的】探讨5,7二甲氧基黄酮(DMF)对人胰腺癌干细胞特性的影响。【方法】体外培养人胰腺癌PANC1细胞系得到微球细胞,流式细胞仪检测;划痕法分析不同浓度DMF对胰腺癌干细胞自我更新、体外细胞迁移和运动能力影响; Western Blot分析不同浓度DMF干预后PANC1细胞系胰腺癌干细胞表面标志物CD133、CD44、ALDH1、Bmil、Ecad、Ncad蛋白表达变化。【结果】DMF以浓度依赖方式抑制人胰腺癌PANC1细胞系胰腺癌干细胞肿瘤球形成能力及抑制细胞体外迁移能力;DMF以浓度依赖方式使胰腺癌干细胞标志物CD133、CD44、ALDH1、Bmi1、Ncad蛋白表达水平降低,而Ecad蛋白水平升高。【结论】DMF以浓度依赖方式显著抑制人胰腺癌PANC1细胞系胰腺癌样干细胞自我更新、分化后细胞迁移、细胞标志物CD133、CD44、ALDH1、Bmi1、Ncadherin蛋白表达,而增强Ecadherin蛋白表达。
【Objective】To examine the effects of 5,7Dimethoxyflavone (DMF) on the properties of human pancreatic cancer stem cell. 【Methods】Human pancreatic cancer PANC1 cell lines were cultured in vitro to generate mammospheres and then detect phenotypes by flow cytometry. The Scratch method was used to contrast cell migration and movement ability after the influence of different concentrations of DMF on the pancreatic cancer stem cells in vitro. Western blot analysis was used to compare of surface marker CD133, CD44, ALDH1, Bmil, Ecad, and Ncad protein expression levels of human PANC1 pancreatic cancer stem cells after different concentrations of DMF interaction.【Results】DMF in a concentration dependent scenario decreased the sphereforming and migration ability of human PANC1 pancreatic cancer stem cells in vitro. Stem cell marker CD133, CD44, ALDH1, Bmi1, and Ncad protein expression levels were decreased by DMF in a concentration dependent manner, but Ecad protein level increased. 【Conclusion】DMF in a concentration dependent manner significantly inhibited in human PANC1 pancreatic cancer stem cell selfrenewal, cell migration, stem cell markers CD133、 CD44、 ALDH1、 Bmi1 protein expression ,but Ncadherin protein expression increased.
出处
《医学临床研究》
CAS
2016年第4期654-657,共4页
Journal of Clinical Research
基金
[基金项目]湖南省科学技术厅基金项目(2013FJ3146)