犀黄丸提取液对MDA-MB-231乳腺癌细胞功能的影响
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  • 英文篇名:Effect of Xihuang Pill Extracting Solution on MDA-MB-231 Breast Cancer Cell Function
  • 作者:许涛 ; 李萍 ; 曾召琼 ; 易帆 ; 胡燕 ; 苏敏 ; 谢小兵
  • 英文作者:XU Tao;LI Ping;ZENG Zhaoqiong;YI Fan;HU Yan;SU Min;XIE Xiaobing;The First Affliated Hospital of Hunan University of Chinese Medicine;
  • 关键词:犀黄丸 ; 乳腺癌 ; MDA-MB-231细胞 ; 细胞增殖 ; 细胞凋亡
  • 英文关键词:Xihuang Pill;;Breast cancer;;MDA-MB-231 cell;;cell proliferation;;apoptosis
  • 中文刊名:HNZK
  • 英文刊名:Acta Chinese Medicine
  • 机构:湖南中医药大学第一附属医院;
  • 出版日期:2019-05-31 13:15
  • 出版单位:中医学报
  • 年:2019
  • 期:v.34;No.253
  • 基金:国家自然科学基金项目(81703917);; 湖南省自然科学基金项目(2017JJ3242)
  • 语种:中文;
  • 页:HNZK201906025
  • 页数:5
  • CN:06
  • ISSN:41-1411/R
  • 分类号:103-107
摘要
目的:研究犀黄丸提取液对MDA-MB-231乳腺癌细胞功能的影响。方法:采用CCK-8法检测犀黄丸提取液对细胞半抑制浓度(IC50)和细胞活力的影响;采用流式细胞技术检测细胞凋亡;transwell法检测细胞转移能力;采用克隆形成实验检测细胞增殖能力。结果:犀黄丸提取液干预细胞72 h的IC50值为15.08 g·L~(-1);以15.08 g·L~(-1)的犀黄丸提取液干预细胞72 h后,相对未加药组,其细胞活力显著下降(P<0.01),早期凋亡和晚期凋亡均显著升高(P<0.01),细胞迁移和增殖能力均显著下降(P<0.01)。结论:本研究从细胞水平上证实了犀黄丸具有显著促进细胞凋亡、抑制细胞增殖、转移和降低细胞活力的能力。
        Objective:To study the effect of Xihuang Pill extract solution on the function of MDA-MB-231 Breast cancer cells.Methods:CCK-8 assay was used to detect the semi-inhibitory concentration(IC50) and cell viability of Xihuang Pill extract solution;cell apoptosis was detected with flow cytometry;cell transfer ability was detected with transwell assay;cell proliferation was detected with colony formation assay.Results:The IC50 value of Xihuang Pill extract in intervention of cells for 72 h was 15.08 g·L~(-1).After interfering with cells with 15.08 g·L~(-1) of Rhubarb Pills for 72 h,the cell viability was significant compared with the untreated group.Decreased(P<0.01),early apoptosis and late apoptosis were significantly increased(P<0.01),and cell migration and proliferation ability were significantly decreased(P<0.01).Conclusion:This study demonstrates that Xihuang Pill has a significant ability to promote apoptosis,inhibit cell proliferation,metastasis and cell viability at the cellular level.
引文
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