TY - JOUR
T1 - Induction of apoptosis in human leukemia cells by grape seed extract occurs via activation of c-Jun NH 2-terminal kinase
AU - Gao, Ning
AU - Budhraja, Amit
AU - Cheng, Senping
AU - Yao, Hua
AU - Zhang, Zhuo
AU - Shi, Xianglin
PY - 2009/1/1
Y1 - 2009/1/1
N2 - Purpose: To characterize the functional role of c-Jun NH 2-terminal kinase (JNK) and other apoptottc pathways in grape seed extract (GSE)-induced apoptosis in human leukemia cells by using pharmacologic and genetic approaches. Experimental Design: Jurkat cells were treated with various concentrations of GSE for 12 and 24 h or with 50 μg/mL GSE for various time intervals, after which apoptosis, caspase activation, and cell signaling pathways were evaluated. Parallel studies were done in U937 and HL-60 human leukemia cells. Results: Exposure of Jurkat cells to GSE resulted in dose- and time-dependent increase in apoptosis and caspase activation, events associated with the pronounced increase in Cip1/p21 protein level. Furthermore, treatment of Jurkat cells with GSE resulted in marked increase in levels of phospho-JNK. Conversely, interruption of the JNK pathway by pharmacologic inhibitor (e.g., SP600125) or genetic (e.g., small interfering RNA) approaches displayed significant protection against GSE-mediated lethality in Jurkat cells. Conclusions: The result of the present study showed that GSE induces apoptosis in Jurkat cells through a process that involves sustained JNK activation and Cip1/p21 up-regulation, culminating in caspase activation.
AB - Purpose: To characterize the functional role of c-Jun NH 2-terminal kinase (JNK) and other apoptottc pathways in grape seed extract (GSE)-induced apoptosis in human leukemia cells by using pharmacologic and genetic approaches. Experimental Design: Jurkat cells were treated with various concentrations of GSE for 12 and 24 h or with 50 μg/mL GSE for various time intervals, after which apoptosis, caspase activation, and cell signaling pathways were evaluated. Parallel studies were done in U937 and HL-60 human leukemia cells. Results: Exposure of Jurkat cells to GSE resulted in dose- and time-dependent increase in apoptosis and caspase activation, events associated with the pronounced increase in Cip1/p21 protein level. Furthermore, treatment of Jurkat cells with GSE resulted in marked increase in levels of phospho-JNK. Conversely, interruption of the JNK pathway by pharmacologic inhibitor (e.g., SP600125) or genetic (e.g., small interfering RNA) approaches displayed significant protection against GSE-mediated lethality in Jurkat cells. Conclusions: The result of the present study showed that GSE induces apoptosis in Jurkat cells through a process that involves sustained JNK activation and Cip1/p21 up-regulation, culminating in caspase activation.
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U2 - 10.1158/1078-0432.CCR-08-1447
DO - 10.1158/1078-0432.CCR-08-1447
M3 - Article
C2 - 19118041
AN - SCOPUS:58849106770
SN - 1078-0432
VL - 15
SP - 140
EP - 149
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 1
ER -