Cinobufacini, an aqueous extract from Bufo bufo gargarizans Cantor, induces apoptosis through a mitochondria-mediated pathway in human hepatocellular carcinoma cells

被引:199
作者
Qi, Fanghua [1 ,2 ]
Li, Anyuan [1 ]
Zhao, Lin [1 ]
Xu, Huanli [2 ]
Inagaki, Yoshinori [2 ]
Wang, Dongliang [2 ]
Cui, Xiaoyan [2 ]
Gao, Bo [3 ]
Kokudo, Norihiro [2 ]
Nakata, Munehiro [4 ]
Tang, Wei [2 ]
机构
[1] Shandong Univ, Prov Hosp, Dept Tradit Chinese Med, Jinan 250021, Peoples R China
[2] Univ Tokyo, Hepatobiliary Pancreat Surg Div, Dept Surg, Grad Sch Med, Tokyo 1138655, Japan
[3] Anhui Jinchan Biochem Co Ltd, Huaibei 235000, Peoples R China
[4] Tokai Univ, Dept Appl Biochem, Kanagawa 2591292, Japan
关键词
Cinobufacini; Bufo bufo gargarizans Cantor; Apoptosis; Human hepatocellular carcinoma cell lines; Mitochondria; Caspase; CANCER-THERAPY; BCL-2; FAMILY; CYTOCHROME-C; IN-VITRO; INDUCTION; PROTEINS; VIVO;
D O I
10.1016/j.jep.2010.02.022
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Aim of the study: Cinobufacini (Huachansu), an aqueous extract from the skin and parotid venom glands of Bufo bufo gargarizans Cantor, is a traditional Chinese medicine widely used in clinical cancer therapy in China. The present study sought to investigate the possible signaling pathway implicated in cinobufacini-induced apoptosis in the hepatocellular carcinoma cell lines HepG(2) and Bcl-7402. Materials and methods: The effects of cinobufacini on cell proliferation of HepG2 and Bel-7402 cells were evaluated by 3-[4,5-dimethylthiazol-2-y1]-2,5-diphenyl-tetrazolium bromide (MU) assays. Cell apoptosis was detected by Hoechst 33258 staining and flow cytometry analysis. The mitochondrial membrane potential (Delta psi m) and caspase-9 and -3 activity were detected using MitoCapture reagent staining and colorimetric assays, respectively. The expression of apoptosis-related proteins and release of cytochrome c were assessed by Western blot analysis. Results: Cinobufacini significantly inhibited cell proliferation of both cell lines in a dose- and time-dependent manner. Marked changes in apoptotic morphology and apoptosis rates were clearly observed after cinobufacini treatment. The protein expression of Bax increased whereas that of Bcl-2 decreased, leading to an increase in the Bax/Bcl-2 ratio. Subsequently, cinobufacini disrupted the mitochondrial membrane potential (Delta psi m) and resulted in the release of cytochrome c, activation of both caspase-9 and -3, and cleavage of poly (ADP-ribose) polymerase (PARP). Conclusion: The present study indicated that cinobufacini can induce apoptosis of HepG2 and Bcl-7402 cells through a mitochondria-mediated apoptosis pathway. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:654 / 661
页数:8
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