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雷公藤内酯醇抑制A375细胞增殖和迁移及CCR7表达的体外实验
引用本文:吴凤,高君,夏颖,朱里,钱悦,涂亚庭,黄长征,陈思远.雷公藤内酯醇抑制A375细胞增殖和迁移及CCR7表达的体外实验[J].中国皮肤性病学杂志,2012,26(5):373-375,382.
作者姓名:吴凤  高君  夏颖  朱里  钱悦  涂亚庭  黄长征  陈思远
作者单位:华中科技大学同济医学院附属协和医院皮肤科,湖北武汉,430022
摘    要:目的观察雷公藤内酯醇在体外抑制人黑素瘤细胞A375增殖和迁移的能力及对细胞表面趋化因子受体CCR7表达的影响情况,初步分析其作用机制。方法用CCK-8比色试剂盒检测雷公藤内酯醇对A375细胞增殖的作用,Transwell微孔隔离小室迁移实验检测雷公藤内酯醇对A375细胞体外迁移能力的影响,Western blot法检测雷公藤内酯醇对A375细胞CCR7蛋白表达的影响。结果雷公藤内酯醇以剂量依赖方式抑制A375细胞的增殖,24h的IC50值为0.20μg/mL;雷公藤内酯醇能显著地抑制A375细胞的体外迁移能力(P0.01),侵袭抑制率约为82.84%;经不同浓度雷公藤内酯醇(0μg/mL,0.2μg/mL和0.4μg/mL)处理后,A375细胞中CCR7蛋白表达呈明显下降趋势(P0.05)。结论雷公藤内酯醇具有抗A375细胞增殖和体外迁移能力的作用,其机制可能与下调其表面趋化因子受体CCR7的表达相关,并且该作用呈一定的浓度依赖性。

关 键 词:雷公藤内酯醇  A375细胞  细胞增殖  细胞迁移  CCR7

The Inhibitory Effects of Triptolide on Cell Proliferation, Migration and the CCR7 Expression of A375 Cells in Vitro
WU Feng , GAO Jun , XIA Ying , ZHU Li , QIAN Yue , TU Ya-ting , HUANG Chang-zheng , CHEN Si-yuan.The Inhibitory Effects of Triptolide on Cell Proliferation, Migration and the CCR7 Expression of A375 Cells in Vitro[J].The Chinese Journal of Dermatovenereology,2012,26(5):373-375,382.
Authors:WU Feng  GAO Jun  XIA Ying  ZHU Li  QIAN Yue  TU Ya-ting  HUANG Chang-zheng  CHEN Si-yuan
Institution:(Department of Dermatology, Union Hospital, Tongji Medical College,Huazhong University of Science and Technology, Wuhan 430022,China)
Abstract:Objective To investigate the inhibitory effects of triptolide on cell proliferation and metastasis of human melanoma cell line A375 and the effects of triptolide on CC-chemokine receptor 7(CCR7) expression, and to discuss the potential anti-tumour mechanisms of TPL in vitro theoretically. Methods The effects of triptolide on the proliferation and migration of A375 cells were detected by the Cell Counting Kit-8(CCK-8)assay and Transwell chamber respectively. The effect of different concentration of Triptolide on CCR7 protein expression of A375 cells was studied by Western blot. Results Triptolide inhibited the proliferation of A375 cells in a dose-dependent way with a 24h IC50 value of 0.20μg/mL. The migration ability of A375 cells was significantly blocked by triptolide with an invasion-inhibition ratio of 82.85%(P<0.01). Triptolide could significantly downregulate the expression of CCR7 on A375 cells in a dose-dependent manner. Conclusion Triptolide could inhibit the cell proliferation and migration of A375 cells in vitro in a dose-dependent way, and the potential mechanism might be related to the downregulation of CCR7 expression of A375 cells.
Keywords:Triptolide  A375  Cell proliferation  Cell migration  CCR7
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