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Lignans inhibit cell growth via regulation of Wnt/beta-catenin signaling

Authors
Yoo, Ji-HyeLee, Hee JuKang, KyungsuJho, Eun HyeKim, Chul YoungBaturen, DulamjavTunsag, JigjidsurenNho, Chu Won
Issue Date
Aug-2010
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Lignans; Arctigenin; Arctiin; Matairesinol; Wnt/beta-catenin signaling; Colon cancer
Citation
FOOD AND CHEMICAL TOXICOLOGY, v.48, no.8-9, pp.2247 - 2252
Indexed
SCIE
SCOPUS
Journal Title
FOOD AND CHEMICAL TOXICOLOGY
Volume
48
Number
8-9
Start Page
2247
End Page
2252
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/39607
DOI
10.1016/j.fct.2010.05.056
ISSN
0278-6915
Abstract
As aberrant activation of Wnt/beta-catenin signaling is one of the major mechanisms of carcinogenesis in colon cancer, identification of inhibitors of this pathway may aid in colon cancer prevention. We investigated the ability of the lignans arctiin, matairesinol and arctigenin from Saussurea salicifolia to inhibit Wnt/beta-catenin signaling in SW480 human colon cancer cells. The lignans inhibited SW480 cell growth. In addition, the transcriptional activity of a reporter construct containing the TCF binding element (TBE) was decreased after the treatment with all three lignans. Although arctiin, matairesinol and arctigenin have similar structures, arctigenin affected Wnt/beta-catenin signaling most significantly. Further, arctigenin reduced the level of beta-catenin by inducing its phosphorylation and thus its degradation. Arctigenin also decreased expression of the beta-catenin/TCF downstream genes CCND1, survivin and CTNNB1, and induced apoptosis. These results suggest that arctigenin, an aglycone with a methoxyl group, potently inhibits the growth of human colon cancer cells via the Wnt/beta-catenin signaling pathway. (C) 2010 Published by Elsevier Ltd.
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