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Gleditsia sinensis Thorn Extract Inhibits Human Colon Cancer Cells: The Role of ERK1/2, G2/M-Phase Cell Cycle Arrest and p53 Expression

Authors
Lee, Se-JungPark, KeerangHa, Sang-DoKim, Wun-JaeMoon, Sung-Kwon
Issue Date
Dec-2010
Publisher
WILEY
Keywords
water extract of Gleditsia sinensis thorns; xenografts; p53; ERK; G2/M-phase cell cycle arrest; cell growth
Citation
PHYTOTHERAPY RESEARCH, v.24, no.12, pp 1870 - 1876
Pages
7
Journal Title
PHYTOTHERAPY RESEARCH
Volume
24
Number
12
Start Page
1870
End Page
1876
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22024
DOI
10.1002/ptr.3214
ISSN
0951-418X
1099-1573
Abstract
The thorns of Gleditsia sinensis are used as a medicinal herb in China and Korea. However, the mechanisms responsible for the antitumor effects of the water extract of Gleditsia sinensis thorns (WEGS) remain unknown. HCT116 cells treated with the WEGS at a dose of 800 mu g/mL (IC50) showed a significant decrease in cell growth and an increase in cell cycle arrest during the G2/M-phase. G2/M-phase arrest was correlated with increased p53 levels and down-regulation of the check-point proteins, cyclinB1, Cdc2 and Cdc25c. In addition, treatment with WEGS induced phosphorylation of extracellular signal-regulated kinase (ERK), p38 MAP kinase and JNK (c-Jun N-terminal kinases). Moreover, inhibition of ERK by treatment of cells with the ERK-specific inhibitor PD98059 blocked WEGS-mediated p53 expression. Similarly, blockage of ERK function in the WEGS-treated cells reversed cell-growth inhibition and decreased cell cycle proteins. Finally, in vivo WEGS treatment significantly inhibited the growth of HCT116 tumor cell xenografts in nude mice with no negative side effects, including loss of body weight. These results describe the molecular mechanisms whereby the WEGS might inhibit proliferation of colon cancer both in vitro and in vivo, suggesting that WEGS has potential as an anticancer agent for the treatment of malignancies. Copyright (C) 2010 John Wiley & Sons, Ltd.
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대학원 (식품생명공학과)
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