The anti-migration and anti-invasion effects of Bruceine D in human triple-negative breast cancer MDA-MB-231 cells

被引:35
作者
Luo, Can [1 ]
Wang, Yu [2 ]
Wei, Cheng [2 ]
Chen, Yuxin [3 ]
Ji, Zhaoning [1 ]
机构
[1] Yijishan Hosp, Wannan Med Coll, Dept Oncol, 2 Zheshan West Rd, Wuhu 241001, Anhui, Peoples R China
[2] Wannan Med Coll, Dept Oncol, Wuhu 241001, Anhui, Peoples R China
[3] Soochow Univ, Gaoyou Hosp, Gaoyou Peoples Hosp, Dept Oncol, Gaoyou 225600, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Bruceine D; triple-negative breast cancer; migration; invasion; epithelial-mesenchymal transition; PI3K/AKT; EPITHELIAL-MESENCHYMAL TRANSITION; VIMENTIN EXPRESSION; E-CADHERIN; PATHWAY; METASTASIS; ACTIVATION; APOPTOSIS; INVOLVEMENT; BIOLOGY; SYSTEM;
D O I
10.3892/etm.2019.8187
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Brucein D (BD) is a naturally occurring major active quassinoid extracted from the Chinese medicinal herb Brucea javanica, which has been previously demonstrated to exhibit anticancer activities. The present study aimed to investigate the anticancer effects of BD on MDA-MB-231 cells, a human triple-negative breast cancer (TNBC) cell line. An MTT assay was performed to assess cell viability, whilst wound healing and Transwell assay were applied to measure cell migration and invasion, respectively. Western blot analysis was performed to assess the expression of E-cadherin, vimentin and beta-catenin, which are proteins associated with epithelial-mesenchymal transformation (EMT), and PI3K, AKT and p-AKT, which are key components of the PI3K/AKT signaling pathway. BD was indicated to reduce cell viability in a dose- and time-dependent manner, whilst cell invasion and migration were also significantly inhibited in a dose-dependent manner. Western blot analysis demonstrated that BD treatment significantly upregulated the expression of E-cadherin and downregulated the expression of vimentin and beta-catenin. Additionally, BD downregulated the expression of PI3K and reduced AKT phosphorylation. In conclusion, BD can inhibit MDA-MB-231 cell viability, migration and invasion, suggesting the potential use of BD for the treatment of TNBC.
引用
收藏
页码:273 / 279
页数:7
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