Selective induction of apoptosis through activation of caspase-8 in human leukemia cells (Jurkat) by dandelion root extract

被引:68
作者
Ovadje, P. [1 ]
Chatterjee, S. [1 ]
Griffin, C. [1 ]
Tran, C. [1 ]
Hamm, C. [2 ]
Pandey, S. [1 ]
机构
[1] Univ Windsor, Dept Chem & Biochem, Windsor, ON N9B 3P4, Canada
[2] Windsor Reg Canc Ctr, Windsor, ON, Canada
关键词
Dandelion root extract; Caspase-8; Apoptosis; Mitochondria; Human leukemia; BASIC BIOLOGICAL PHENOMENON; WIDE-RANGING IMPLICATIONS; TARAXACUM-OFFICINALE; MITOCHONDRIA; CYTOTOXICITY; RESISTANCE; ALPHA; ASSAY;
D O I
10.1016/j.jep.2010.09.005
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of study: Dandelion extracts have been used in traditional Native American Medicine and Traditional Chinese Medicine (TCM) for treatment of leukemia and breast cancer; however, the mechanism of action remains unknown. Today, DRE is mainly marketed for management of gastrointestinal and liver disorders. The current study aims to determine the anti-cancer activity of dandelion root extract (DRE) against human leukemia, and to evaluate the specificity and mechanism of DRE-induced apoptosis. Materials and methods: The effect of DRE on cell viability was evaluated using the colorimetric-based WST-1 assay. Apoptotic cell death was monitored by nuclear condensation and confirmed by exposure of phosphatidylserine to outer leaflet of plasma membrane. Activation of caspases was detected using a fluorogenic substrate specific to either caspase-8 or -3. Loss of mitochondrial membrane potential was observed by microscopy using JC-1 dye. The apoptotic effect of DRE was also evaluated on a dominant-negative FADD (Fas-associated death domain) cell line and non-cancerous peripheral blood mononuclear cells (PBMCs). Results: Aqueous DRE effectively induces apoptosis in human leukemia cell lines in a dose and time dependent manner. Very early activation of caspase-8 and the subsequent activation of caspase-3 indicate that DRE may be inducing extrinsic or receptor-mediated apoptosis. Caspase inhibition rendered this extract ineffective, thus DRE-induced apoptosis is caspase-dependent. Moreover, the dominant-negative FADD cells that are unable to form a complete DISC (death-inducing signaling complex) were resistant to DRE treatment, which further confirms our hypothesis that DRE induces receptor-mediated apoptosis. Interestingly, non-cancerous peripheral blood mononuclear cells (PBMCs) exposed to aqueous DRE under the same treatment conditions as leukemia cells were not significantly affected. Conclusion: Our results suggest that aqueous DRE contains components that act to induce apoptosis selectively in cultured leukemia cells, emphasizing the importance of this traditional medicine and thus presents a potential novel non-toxic alternative to conventional leukemia therapy. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:86 / 91
页数:6
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