Negative regulation of β-catenin/Tcf signaling by naringenin in AGS gastric cancer cell

被引:43
作者
Lee, JH [1 ]
Park, CH [1 ]
Jung, KC [1 ]
Rhee, HS [1 ]
Yang, CH [1 ]
机构
[1] Seoul Natl Univ, Div Chem & Mol Engn, Seoul 151742, South Korea
关键词
beta-catenin/Tcf signaling; naringenin; nuclear beta-catenin; mechanism;
D O I
10.1016/j.bbrc.2005.07.146
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Functional activation of beta-catenin/Tcf signaling plays an important role in early events in carcinogenesis. We examined the effect of naringenin against beta-catenin/Tcf signaling in gastric cancer cells. Reporter gene assay showed that naringenin inhibited beta-catenin/Tcf signaling efficiently. In addition, the inhibition of beta-catenin/Tcf signaling by naringenin in HEK293 cells transiently transfected with constitutively mutant beta-catenin gene, whose product is not phosphorylated by GSK3 beta, indicates that its inhibitory mechanism was related to beta-catenin itself or downstream components. To investigate the precise inhibitory mechanism, we performed immunofluorescence, Western blot, and EMSA. As a result, our data revealed that the beta-catcnin distribution and the levels of nuclear beta-catenin and Tcf-4 proteins were unchanged after naringenin treatment. Moreover, the binding activities of Tcf complexes to consensus DNA were not affected by naringenin. Taken together, these data suggest that naringenin inhibits beta-catenin/Tcf signaling in gastric cancer with unknown mechanisms. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:771 / 776
页数:6
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