Essential oil of Curcuma wenyujin induces apoptosis in human hepatoma cells
被引:78
作者:
Xiao, Yu
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Univ Macau, Inst Chinese Med Sci, Taipa, Macao, Peoples R China
Sichuan Acad Med Sci, Sichuan Prov Peoples Hosp, State Drug Clin Trial Agcy, Sci & Technol Dept, Chengdu 610072, Sichuan Prov, Peoples R ChinaUniv Macau, Inst Chinese Med Sci, Taipa, Macao, Peoples R China
Xiao, Yu
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,2
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Yang, Feng-Qing
[1
]
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Li, Shao-Ping
[1
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Hu, Guang
[1
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Lee, Simon Ming-Yuen
[1
,3
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Wang, Yi-Tao
[1
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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 610072, Sichuan Prov, Peoples R China
[3] Chinese Univ Hong Kong, Inst Chinese Med, Hong Kong, Hong Kong, Peoples R China
AIM: To investigate the effects of the essential oil of Curcuma wenyujin (CWO) on growth inhibition and on the induction of apoptosis in human HepG2 cancer cells. METHODS: The cytotoxic effect of drugs on HepG2 cells was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetra-zolium bromide (MTT) assay. DNA fragmentation was visualized by agarose gel electrophoresis. Cell cycle and mitochondrial transmembrane potential (Delta psi m) were determined by flow cytometry (FCM). Cytochrome C immunostaining was evaluated by fluorescence microscopy. Caspase-3 enzymatic activity was assayed by the cleavage of Ac-DEVD-R110. Cleaved PARP and active caspase-3 protein levels were measured by FCM using BD (TM) CBA Human Apoptosis Kit. RESULTS: Treatment with CWO inhibited the growth of HepG2 cells in a dose-dependent mariner, and the IC50 of CWO was approximately 70 mu g/mL. CWO was found to inhibit the growth of HepG2 cells by inducing a cell cycle arrest at S/G(2). DNA fragmentation was evidently observed at 70 mu g/mL after 72 h of treatment. During the process, cytosolic HepG2 cytochrome C staining showed a markedly stronger green fluorescence than in control cells in a dose-dependent fashion, and CWO also caused mitochondrial transmembrane depolarization. Furthermore, the results clearly demonstrated that both, activity of caspase-3 enzyme and protein levels of cleaved PARP, significantly increased in a dose-dependent manner after treatment with CWO. CONCLUSION: CWO exhibits an antiproliferative effect in HepG2 cells by inducing apoptosis. This growth inhibition is associated with cell cycle arrest, cytochrome C translocation, caspase 3 activation, Poly-ADP-ribose polymerase (PARP) degradation, and loss of mitochondrial membrane potential. This process involves a mitochondria-caspase dependent apoptosis pathway. As apoptosis is an important anti-cancer therapeutic target, these results suggest a potential of CWO as a chemotherapeutic agent. (c) 2008 The WJG Press. All rights reserved.