Oleanolic acid potentiates the antitumor activity of 5-fluorouracil in pancreatic cancer cells

被引:39
|
作者
Wei, Jianteng [1 ,3 ]
Liu, Haizhou [1 ]
Liu, Ming [1 ]
Wu, Ning [1 ]
Zhao, Jin [1 ,3 ]
Xiao, Lin [1 ,3 ]
Han, Lijun [1 ]
Chu, Edward [4 ]
Lin, Xiukun [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, Qingdao 266071, Peoples R China
[2] Capital Med Univ, Dept Pharmacol, Beijing 100069, Peoples R China
[3] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
[4] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15232 USA
关键词
apoptosis; oleanolic acid; 5-fluorouracil; pancreatic cancer cells; synergism; CARCINOMA CELLS; CYTOCHROME-C; URSOLIC ACID; APOPTOSIS; ACTIVATION; GROWTH; DEATH; PACLITAXEL; INDUCTION; RELEASE;
D O I
10.3892/or.2012.1921
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The antitumor activity of oleanolic (OA) has attracted attention due to its marked antitumor effects and pharmacological safety. In the present study, the effects of the combination of OA and 5-fluorouracil (5-FU) on Panc-28 human pancreatic cells were studied. The results showed that combined use of OA and 5-FU synergistically potentiated cell death effects on Panc-28 cells, and the pro-apoptotic effects were also increased. Further study revealed that the combined treatment could enhance mitochondrial depolarization, lysosomal membrane permeabilization (LMP) and leakage of cathepin D, while the release of cytochrome C did not display significant changes. The expression of apoptosis related proteins was also affected in cells treated with the combination of OA and 5-FU, including activation of caspases-3 and the expression of Bcl-2/Bax, survivin and NF-kappa B. Our results provide evidence that combination of OA and 5-FU may serve as a novel strategy for the treatment of pancreatic cancer.
引用
收藏
页码:1339 / 1345
页数:7
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