Cyclovirobuxine D Inhibits Cell Proliferation and Induces Mitochondria-Mediated Apoptosis in Human Gastric Cancer Cells

被引:17
|
作者
Wu, Jie [1 ,2 ]
Tan, Zhujun [3 ]
Chen, Jian [4 ]
Dong, Cheng [1 ,5 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Naval Architecture Ocean & Civil Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Minist Educ China MOE, Key Lab Hydrodynam, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Gen Surg, Sch Med, Shanghai 200092, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
[5] Penn State Univ, Dept Biomed Engn, University Pk, PA 16802 USA
基金
中国国家自然科学基金;
关键词
cyclovirobuxine D; cell cycle; gastric cancer; apoptosis; mitochondria; JAK-STAT; CALCIUM; DIFFERENTIATION; EXPRESSION; SURVIVAL; PATHWAY;
D O I
10.3390/molecules201119729
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gastric cancer is one of the most common malignant cancers, with high death rates, poor prognosis and limited treatment methods. Cyclovirobuxine D (CVB-D) is the main active component of the traditional Chinese medicine Buxus microphylla. In the present study, we test the effects of CVB-D on gastric cancer cells and the underlying mechanisms of action. CVB-D reduced cell viability and colony formation ability of MGC-803 and MKN28 cells in a time- and concentration-dependent manner. Flow cytometry showed that cell cycle of CVB-D treated cells was arrested at the S-phase. CVB-D also induced apoptosis in MGC-803 and MKN28 cells, especially early stage apoptosis. Furthermore, mitochondria membrane potential (m) was reduced and apoptosis-related proteins, cleaved Caspase-3 and Bax/Bcl-2, were up-regulated in CVB-D-treated MGC-803 and MKN28 cells. Taken together, our studies found that CVB-D plays important roles in inhibition of gastric tumorigenesis via arresting cell cycle and inducing mitochondria-mediated apoptosis, suggesting the potential application of CVB-D in gastric cancer therapy.
引用
收藏
页码:20659 / 20668
页数:10
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