Dibenzocyclooctadiene lignans, gomisins J and N inhibit the Wnt/β-catenin signaling pathway in HCT116 cells

被引:28
作者
Kang, Kyungsu [1 ]
Lee, Kyung-Mi [1 ]
Yoo, Ji-Hye [1 ]
Lee, Hee Ju [1 ]
Kim, Chul Young [1 ,2 ]
Nho, Chu Won [1 ]
机构
[1] Korea Inst Sci & Technol, Funct Food Ctr, Kangnung 210340, South Korea
[2] Hanyang Univ, Coll Pharm, Ansan 426791, South Korea
关键词
Wnt/beta-catenin; Cancer chemoprevention; Dibenzocyclooctadiene lignan; Schisandra chinensis; Gomisin; Cyclin D1; COLON-CANCER CELLS; SCHISANDRA-CHINENSIS; BETA-CATENIN; SUPPRESSES GROWTH; ACTIVATION; COMPONENTS; APOPTOSIS;
D O I
10.1016/j.bbrc.2012.10.046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Here, we report that gomisin J and gomisin N. clibenzocyclooctadiene type lignans isolated from Sch (sonchinensis, inhibit Wnt/beta-catenin signaling in HCT116 cells. Gomisins J and N appear to inhibit Wnt/Bcatenin signaling by disrupting the interaction between beta-catenin and its specific target DNA sequences (TCF binding elements, TBE) rather than by altering the expression of the beta-catenin protein. Gomisins J and N inhibit HCT116 cell proliferation by arresting the cell cycle at the G0/G1 phase. The G0/G1 phase arrest induced by gomisins J and N appears to be caused by a decrease in the expression of Cyclin D1, a representative target gene of the Wnt/beta-catenin signaling pathway, as well as Cdk2, Cdk4, and E2F-1. Therefore, gomisins J and N, the novel Wnt/beta-catenin inhibitors discovered in this study, may serve as potential agents for the prevention and treatment of human colorectal cancers. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 291
页数:7
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