Critical role of pro-apoptotic Bcl-2 family members in andrographolide-induced apoptosis in human cancer cells

被引:29
作者
Zhou, Jing [1 ]
Zhang, Siyuan [1 ]
Ong, Choon-Nam [1 ]
Shen, Han-Ming [1 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Community Occupat & Family Med, Singapore 117597, Singapore
关键词
andrographolide; Bid; Bax; Bcl-2; family; mitochondria; apoptosis;
D O I
10.1016/j.bcp.2006.04.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Andrographolide (Andro), a diterpenoid lactone isolated from a traditional herbal medicine Andrographis paniculata, is known to possess potent anti-inflammatory activity. In this study, Andro induced apoptosis in human cancer cells via activation of caspase 8 in the extrinsic death receptor pathway and subsequently with the participation of mitochondria. Andro triggered a caspase 8-dependent Bid cleavage, followed by a series of sequential events including Bax conformational change and mitochondrial translocation, cytochrome c release from mitochondria, and activation of caspase 9 and 3. Inhibition of caspase 8 blocked Bid cleavage and Bax conformational change. Consistently, knockdown of Bid protein using small interfering RNA (siRNA) technique suppressed Andro-induced Bax conformational change and apoptosis. In conclusion, the pro-apoptotic Bcl-2 family members (Bid and Bax) are the key mediators in relaying the cell death signaling initiated by Andro from caspase 8 to mitochondria and then to downstream effector caspases, and eventually leading to apoptotic cell death. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:132 / 144
页数:13
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