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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/13624
Title: Periostin activates integrin α5β1 through a PI3K/AKT-dependent, pathway in invasion of cholangiocarcinoma
Authors: Kusumawadee Utispan
Jumaporn Sonongbua
Peti Thuwajit
Siri Chau-In
Chawalit Pairojkul
Sopit Wongkham
Chanitra Thuwajit
Khon Kaen University
Mahidol University
Keywords: Biochemistry, Genetics and Molecular Biology;Medicine
Issue Date: 1-Sep-2012
Citation: International Journal of Oncology. Vol.41, No.3 (2012), 1110-1118
Abstract: Periostin (PN) is mainly produced from stromal fibroblasts in cholangiocarcinoma (CCA) and shows strong impact in cancer promotion. This work aimed to investigate the mechanism that PN uses to drive CCA invasion. It was found that ITGα5β1 and α6β4 showed high expression in non-tumorigenic biliary epithelial cells and in almost all CCA cell lines. PN had preferential binding to CCA cells via ITGα5β1 and blocking this receptor by either neutralizing antibody or siITGα5 could attenuate PN-induced invasion. After PN-ITGα5β1 binding, intracellular pAKT was upregulated whereas there was no change in pERK. Moreover, PN could not activate AKT in condition of treatment with a PI3K inhibitor. These data provide evidence that PN-activated invasion of CCA cells is through the ITGα5β1/PI3K/AKT pathway. Strategies aimed to inhibit this pathway may, thus, provide therapeutic benefits.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84864981474&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/13624
ISSN: 17912423
10196439
Appears in Collections:Scopus 2011-2015

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