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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/35079
Title: Lead compound bearing caffeic scaffold induces EGFR suppression in solid tumor cancer cells
Authors: Chawannuch Mudjupa
Sherif Abdelhamed
Alaa Refaat
Satoru Yokoyama
Ikuo Saiki
Opa Vajragupta
Mahidol University
University of Toyama
Keywords: Agricultural and Biological Sciences;Biochemistry, Genetics and Molecular Biology
Issue Date: 1-Nov-2015
Citation: Journal of Applied Biomedicine. Vol.13, No.4 (2015), 305-317
Abstract: © 2015 Faculty of Health and Social Studies, University of South Bohemia in Ceske Budejovice. Published by Elsevier Sp. z o.o. All rights reserved. A small molecule EGFR inhibitor, 4-(2-(3-(4-(4-(trifluoromethyl)phenyl)thiazol-2-yl)ureido)vinyl)-1,2-phenylene diacetate (CIU1) was designed in silico by using caffeic scaffold as core structure. The designed compound showed anti-proliferative action against different solid tumor cell lines, particularly metastatic breast cancer cells. CIU1 inhibited the growth of EGFR-overexpressing MDA-MB-468 triple-negative breast cancer cells and wild-type non-small-cell lung cancer H460 cells with IC50values of 8.96 μM and 12.98 μM, respectively, these anti-proliferative effects of CIU1 were comparable to gefitinib (a specific EGFR inhibitor) or lapatinib (a dual EGFR and HER2 tyrosine kinase inhibitor). Interestingly CIU1 effectively inhibited the invasive hormone-dependent MCF-7 cancer cells with an IC502.34 μM. The immunoblot analyses revealed that CIU1 induced programmed cell death and suppressed EGFR expression in EGFR-overexpressing breast cancer (MDA-MB468) and lung cancer (PC-9) cells. The findings substantiated our design strategy and demonstrated the potential of CIU1 as new lead for further optimization in the development of anticancer drugs against advanced solid tumors.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84969664314&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/35079
ISSN: 12140287
1214021X
Appears in Collections:Scopus 2011-2015

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