Eriocalyxin B inhibits proliferation and induces apoptosis through downregulation of Bcl-2 and activation of caspase-3 in human bladder cancer cells

被引:2
|
作者
Rasul, Azhar [1 ]
Liu, Jinmei [1 ]
Liu, Ying [2 ]
Millimouno, Faya Martin [1 ]
Wang, Xiaowan [1 ]
Tsuji, Ichiro [3 ]
Yamamura, Takaki [4 ]
Li, Jiang [2 ]
Li, Xiaomeng [1 ]
机构
[1] NE Normal Univ, Sch Life Sci, Inst Cytol & Genet, MOE,Key Lab Mol Epigenet, Changchun 130024, Peoples R China
[2] Jilin Univ, Dent Hosp, Changchun 130041, Peoples R China
[3] Tohoku Univ, Dept Publ Hlth, Sendai, Miyagi 9808576, Japan
[4] Morioka Coll, Takizawa, Iwate, Japan
基金
中国国家自然科学基金;
关键词
Apoptosis; Bladder cancer; Eriocalyxin B; T24; cells; GASTRIC ADENOCARCINOMA CELLS; CYTOCHROME-C; CYCLE ARREST; MITOCHONDRIAL; COSTUNOLIDE; INDUCTION; PATHWAYS;
D O I
10.3329/bjp.v8i2.13797
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eriocalyxin B (EriB) has been shown to possess promising anticancer potential against various cancer cells. However, its effect against bladder cancer cells remained unexplored. In this study, for the first time, we investigated the effects of EriB on cell proliferation, cell cycle, and apoptosis in bladder cancer T24 cells. In order to examine the effects of EriB on cell proliferation, cell cycle, and apoptosis, we performed MTT assay, flow cytometric analysis and western blot. The results revealed that EriB decreased the cell viability of T24 cells. Flow cytometric analysis demonstrated that EriB markedly induced apoptosis of T24 cells and arrested cell cycle at G2/M phase in a dose-dependent manner. Further characterization showed that EriB involved in the down-regulation of Bcl-2 and activation of caspase-3 before culminating in apoptosis in EriB-treated T24 cells. These in vitro results suggested that EriB should be further examined for in vivo activity in human bladder cancer..
引用
收藏
页码:116 / 123
页数:8
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