Furanodiene induces G2/M cell cycle arrest and apoptosis through MAPK signaling and mitochondria-caspase pathway in human hepatocellular carcinoma cells

被引:90
作者
Xiao, Yu
Yang, Feng-Qing
Li, Shao-Ping
Gao, Jian-Li
Hu, Guang
Lao, Sin-Cheng
Conceicao, Emilia Leong
Fung, Kwok-Pui
Wang, Yi-Tao
Lee, Simon Ming-Yuen [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, Taipa, Macao, Peoples R China
[2] Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, State Drug Clin Trial Agcy, Sci & Technol Dept, Chengdu, Peoples R China
[3] Chinese Univ Hong Kong, Dept Biochem, Hong Kong, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Inst Chinese Med, Hong Kong, Hong Kong, Peoples R China
关键词
furanodiene; apoptosis; HepG(2); caspase-3; mitochondrial; cytochrome c; p38; ERK;
D O I
10.4161/cbt.6.7.4317
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Furanodiene (C15H20O), a pure compound isolated from Traditional Chinese medicine, Curcuma wenyujin, named Ezhu in Chinese, which structure was determined on the basis of NMR, MS and UV spectrum. In this study, we attempted to characterize in detail the signaling cascades resulted from furanodiene-induced apoptosis in human hepatoma HepG2 cells. Furanodiene inhibited HepG2 cell growth by causing cell cycle arrest at G(2)/M and inducing apoptosis as evidenced by DNA fragmentation assay. We found that furanodiene induced mitochondrial transmembrane depolarization, release of mitochondrial cytochrome c, activation of caspases-3 and the cleavage of PARP. The furanodiene mediated mitochondria-caspase apoptotic pathway also involved activation of p38 and inhibition of ERK mitogen-activated protein kinase (MAPK) signaling. These results for the first time have identified the biological activity of furanodiene against HepG2 cells and provide rationales for further development of essential oil of Ezhu and its ingredients such as furanodiene on treatment of liver diseases.
引用
收藏
页码:1044 / 1050
页数:7
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