Neferine induces apoptosis of pancreatic cancer cells through p38 MAPK/JNK activation

被引:1
|
作者
Feng, Tielan [1 ]
Chen, Hao [2 ]
Peng, Yaofang [3 ]
Sun, Xiaoming [4 ]
机构
[1] Lanzhou Univ, Hosp 1, Dept Operat Room, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Hosp 1, Dept Canc Ctr, Lanzhou 730000, Gansu, Peoples R China
[3] Lanzhou Univ, Hosp 1, Dept Pharm, Lanzhou 730000, Gansu, Peoples R China
[4] Lanzhou Univ, Hosp 1, Dept Nurse Dept, Lanzhou 730000, Gansu, Peoples R China
关键词
Neferine; Proliferation; Apoptosis; Pancreatic cancer; p38; MAPK/JNK; INHIBITS GROWTH; PROLIFERATION; EXPRESSION; AUTOPHAGY; PROTEINS; PATHWAY; P21;
D O I
10.4314/tjpr.v18i8.7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To investigate the functional role of neferine on pancreatic cancer (PC) cell apoptosis. Methods: The pancreatic cell line, PANC-1 cells, was exposed with different concentration of neferine. CCK8 and flow cytometry (Cell counting kit-8) were carried out to detect cell proliferation and apoptosis. Protein expression was evaluated by western blot. Results: Neferine suppressed cell viability and caused cell cycle arrest of pancreatic cells in a dose-dependent way. The effect of neferine on pancreatic cells was dependent on its ability to regulate the expression of cyclin E, cyclin D1, p21, cleaved caspase-3, cleaved PARP, Bcl-2 and Bax. In addition, neferine treatment induced the apoptosis of PANC-1 cells via promoting the activation of p38 MAPK/JNK signaling pathway. Conclusions: Neferine inhibits cell viability and proliferation, and promotes apoptosis of PC cells by activating p38 MAPK/JNK signaling pathway. These results indicated the potential therapeutic effect of neferine in the treatment of PC.
引用
收藏
页码:1615 / 1619
页数:5
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