Jolkinolide B from Euphorbia fischeriana Steud induces apoptosis in human leukemic U937 cells through PI3K/Akt and XIAP pathways

被引:56
作者
Wang, Jia-He [1 ]
Zhou, Yi-Jun [2 ]
Bai, Xue [1 ]
He, Ping [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Geriatr, Shenyang 110004, Peoples R China
[2] China Med Univ, Affiliated Hosp 4, Dept Endocrinol & Metab, Shenyang 110004, Peoples R China
基金
中国国家自然科学基金;
关键词
apoptosis; caspase; Euphorbia fischeriana Steud; Jolkinolide B; U937; PROSTATE-CANCER CELLS; NF-KAPPA-B; EXPRESSION; INDUCTION; CASPASES; SMAC/DIABLO; ACTIVATION; INHIBITOR; EXTRACT; IAP;
D O I
10.1007/s10059-011-0137-0
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
Jolkinolide B, a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud, is known to induce apoptosis in cancer cells. However, the molecular mechanism of its anti-cancer activity has not been fully elucidated. In the present study, we found that Jolkinolide B reduced cell viability and induced apoptosis in a dose- and timedependent manner in human leukemic U937. The induction of apoptosis was also accompanied by the downregulation of PI3K/Akt and the inhibitor of apoptosis protein (IAP) family proteins. Moreover, we observed that Jolkinolide B treatment resulted in activation of caspase-3 and -9, which may partly explain the anti-cancer activity of Jolkinolide B. Taken together, our study for the first time suggest that Jolkinolide B is able to enhance apoptosis of U937 cells, at least in part, through downregulation of PI3K/Akt and IAP family proteins. Moreover, triggering of caspase-3 and -9 activation mediated apoptotic induction.
引用
收藏
页码:451 / 457
页数:7
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