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
2010-08
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
FOOD AND CHEMICAL TOXICOLOGY, v.48, no.8-9, pp.2247 - 2252
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.
Keywords
COLORECTAL-CANCER PREVENTION; INDUCE APOPTOSIS; TUMOR-CELLS; CYCLIN D1; OLIVE OIL; RISK; THERAPEUTICS; ANTIOXIDANT; DERIVATIVES; ACTIVATION; COLORECTAL-CANCER PREVENTION; INDUCE APOPTOSIS; TUMOR-CELLS; CYCLIN D1; OLIVE OIL; RISK; THERAPEUTICS; ANTIOXIDANT; DERIVATIVES; ACTIVATION; Lignans; Arctigenin; Arctiin; Matairesinol; Wnt/beta-catenin signaling; Colon cancer
ISSN
0278-6915
URI
https://pubs.kist.re.kr/handle/201004/131209
DOI
10.1016/j.fct.2010.05.056
Appears in Collections:
KIST Article > 2010
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