Down-modulation of Bcl-XL, release of cytochrome c and sequential activation of caspases during honokiol-induced apoptosis in human squamous lung cancer CH27 cells

被引:128
作者
Yang, SE
Hsieh, MT
Tsai, TH
Hsu, SL
机构
[1] Taichung Vet Gen Hosp, Dept Educ & Res, Taichung 40705, Taiwan
[2] China Med Coll, Inst Chinese Pharmaceut Sci, Taichung, Taiwan
[3] Natl Res Inst Chinese Med, Taipei 11221, Taiwan
关键词
apoptosis; Bad; Bcl-X-L; caspase; cytochrome c; honokiol;
D O I
10.1016/S0006-2952(02)00894-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Honokiol is a phenolic compound purified from Magnolia officinalis, which induced the apoptotic cell death in several types of human cancer cells. In the present study, the molecular mechanism of honokiol-mediated apoptotic process was examined in human squamous lung cancer CH27 cells. Here, we found that honokiol-induced apoptotic cell death was accompanied by upregulation of Bad and downregulation of Bcl-X-L, while honokiol had no effect on the levels of Bcl-2, Bcl-X-S, Bag-1, Bax and Bak proteins. Moreover, honokiol treatment caused the release of mitochondrial cytochrome c to cytosol and sequential activation of caspases. Proteolytic activation of caspase-3 and cleavage of PARP, an in vivo substrate for caspase-3, were observed in honokiol-treated CH27 cells. Furthermore, treatment with caspase inhibitors z-DEVD-fmk and z-VAD-fmk markedly blocked honokiol-induced apoptosis. These results demonstrated that modulation of Bcl-XL and Bad proteins, release of mitochondrial cytochrome c and activation of caspase-3, participated in honokiol-triggered apoptotic process in human squamous lung cancer CH27 cells. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1641 / 1651
页数:11
相关论文
共 71 条
[71]   Apaf-1, a human protein homologous to C-elegans CED-4, participates in cytochrome c-dependent activation of caspase-3 [J].
Zou, H ;
Henzel, WJ ;
Liu, XS ;
Lutschg, A ;
Wang, XD .
CELL, 1997, 90 (03) :405-413