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中国临床药理学与治疗学 ›› 2018, Vol. 23 ›› Issue (1): 13-17.doi: 10.12092/j.issn.1009-2501.2018.01.003

• 基础研究 • 上一篇    下一篇

氧化苦参碱通过调控上皮间质转化抑制三阴性乳腺癌细胞侵袭转移

蔡加琴,魏晓霞,黄旭慧,庄 捷,孙 红   

  1. 福建省立医院药学部,福州 350001,福建
  • 收稿日期:2017-06-21 修回日期:2017-07-21 出版日期:2018-01-26 发布日期:2018-02-07
  • 通讯作者: 孙红,女,博士,副主任药师,研究方向:肿瘤药理学。 Tel:0591-88216352E-mail:sunhong7777@126.com
  • 作者简介:蔡加琴,女,硕士,主管药师,研究方向:肿瘤药理学。 Tel:18259178683 E-mail:jiaqincai@163.com
  • 基金资助:

    国家自然科学基金(81403021);福建省卫生计生青年科研课题(2016-1-7);福建医科大学启航基金项目计划(2016QH107)

Oxymatrine inhibits invasion and metastasis of triple-negative breast cancer cells by regulating epithelial mesenchymal transition

CAI Jiaqin, WEI Xiaoxia, HUANG Xuhui, ZHUANG Jie, SUN Hong   

  1. Department of Pharmacy, Fujian Provincial Hospital, Fuzhou 350001, Fujian, China
  • Received:2017-06-21 Revised:2017-07-21 Online:2018-01-26 Published:2018-02-07

摘要:

目的: 探讨氧化苦参碱对三阴性乳腺癌细胞MDA-MB-231生长增殖及其对迁移能力的影响和机制。方法: CCK-8活细胞计数法分析氧化苦参碱不同浓度(0、1、2、4、6、8、10、20 mg/mL)在不同时间(24、48、72 h)对三阴性乳腺癌细胞MDA-MB-231生长增殖的影响,流式细胞仪检测细胞周期和凋亡,Transwell法观察氧化苦参碱对MDA-MB-231细胞迁移和侵袭能力的影响,Q-PCR法检测EMT相关因子Snail-2和E-cadherin表达水平。结果: 与对照组比较,浓度为2、4、6、8、10、20 mg/mL的氧化苦参碱处理MDA-MB-231细胞24、48和72 h后,对细胞的生长呈时间和剂量依赖性的抑制作用。流式细胞实验提示2 mg/mL氧化苦参碱可使G0/G1期细胞数明显增加(P<0.05),S期和G2/M期的细胞数明显减少(P<0.05),细胞生长阻滞于G0/G1期。中、高浓度氧化苦参碱(4 mg/mL、6 mg/mL)处理12 h能明显抑制MDA-MB-231的侵袭能力,抑制Snail2 mRNA的表达(P<0.01),上调E-cadherin mRNA和蛋白水平的表达(P<0.01)。结论: 氧化苦参碱对三阴性乳腺癌细胞生长和迁移侵袭有抑制作用,具有潜在的抗肿瘤生长和转移作用。

关键词: 氧化苦参碱, 人三阴性乳腺癌, 上皮间质转化, 侵袭, 生长抑制

Abstract:

AIM: To study the inhibitory effects of oxymatrine on growth and migration of human triple-negative breast cancer MDA-MB-231 cell.  METHODS: CCK-8 assay was used to detect the inhibitory effects of oxymatrine on the growth of MDA-MB-231 cells. Inhibitory effect of oxymatrine on cell cycle of MDA-MB-231 cells was detected by flow cytometry (FCM). Effect of oxymatrine on migration of MDA-MB-231 cells was detected by scratch experimental. RESULTS: Compared with the control group, the growth of MDA-MB-231 cells decreased significantly in a time- and dose-dependent manner after oxymatrine treatment (2, 4, 6, 8, 10, 20 mg/mL for 24, 48 and 72 h). Oxymatrine significantly increased the number of cells in G0/G1 phase and decreased the number of cells in S and G2/M phase(P<0.05). Transwell showed that oxymatrine treated MDA-MB-231 cells for 12 h significantly inhibited the invasion of MDA-MB-231. The high concentration of oxymatrine significantly up-regulated the expression of E-cadherin and inhibited the expression of Snail-2 mRNA (P<0.01). CONCLUSION: Oxymatrine exerts its antitumor effect by inhibiting the growth and invasion of MDA-MB-231 cells, which plays a potential role on anti-tumor growth and metastasis.

Key words: oxymatrine, triple-negative breast cancer cells, EMT, migration, growth inhibition

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