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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/47311
Title: A silyl andrographolide analogue suppresses Wnt/β-catenin signaling pathway in colon cancer
Authors: Somrudee Reabroi
Arthit Chairoungdua
Rungnapha Saeeng
Teerapich Kasemsuk
Witchuda Saengsawang
Weiming Zhu
Pawinee Piyachaturawat
Rambhai Barni Rajabhat University
Ocean University of China
Mahidol University
Burapha University
Keywords: Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-May-2018
Citation: Biomedicine and Pharmacotherapy. Vol.101, (2018), 414-421
Abstract: © 2018 Elsevier Masson SAS Hyperactivation of Wnt/β-catenin signaling implicated in oncogenesis of colorectal cancer (CRC) is a potential molecular target for chemotherapy. An andrographolide analogue, 3A.1 (19-tert-butyldiphenylsilyl-8, 17-epoxy andrographolide) has previously been reported to be potently cytotoxic toward cancer cells by unknown molecular mechanisms. The present study explored the anti-cancer activity of analogue 3A.1 on Wnt/β-catenin signaling in colon cancer cells (HT29 cells) which were more sensitive to the others (HCT116 and SW480 cells). Analogue 3A.1 inhibited viability of HT29 cells with IC 50 value of 11.1 ± 1.4 μM at 24 h, which was more potent than that of the parent andrographolide. Analogue 3A.1 also suppressed the proliferation of HT29 cells and induced cell apoptosis in a dose-dependent manner. Its apoptotic activity was accompanied with increased expressions of proteins related to DNA damages; PARP-1 and γ-H2AX. In addition, analogue 3A.1 significantly inhibited T-cell factor and lymphoid enhancer factor (TCF/LEF) promoter activity of Wnt/β-catenin signaling. Accordingly, the expressions of Wnt target genes and β-catenin protein were suppressed. Moreover, analogue 3A.1 increased the activity of GSK-3β kinase, which is a negative regulator responsible for degradation of intracellular β-catenin. This mode of action was further supported by the absence of the effects after treatment with a GSK-3β inhibitor, and over-expression of a mutant β-catenin (S33Y). Our findings reveal, for the first time, an insight into the molecular mechanism of the anti-cancer activity of analogue 3A.1 through the inhibition of Wnt/β-catenin/GSK-3β pathway and provide a therapeutic potential of the andrographolide analogue 3A.1 in CRC treatment.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85042666621&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/47311
ISSN: 19506007
07533322
Appears in Collections:Scopus 2018

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