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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/15777


    Title: Prostaglandin E2/EP1 signaling pathway enhances intercellular adhesion molecule 1 (ICAM-1) expression and cell motility in oral cancer cells.
    Authors: SF, Yang
    MK, Chen
    YS, Hsieh
    TT, Chung
    YH, Hsieh
    CW, Lin
    JL, Su
    MH, Tsai
    CH, Tang
    Contributors: 中山醫大口腔科學研究所
    Date: 2010-06-20
    Issue Date: 2016-08-11T07:37:50Z (UTC)
    ISSN: 0021-9258
    Abstract: Oral squamous cell carcinoma has a striking tendency to migrate and metastasize. Cyclooxygenase (COX)-2, the inducible isoform of prostaglandin (PG) synthase, has been implicated in tumor metastasis. However, the effects of COX-2 on human oral cancer cells are largely unknown. We found that overexpression of COX-2 or exogenous PGE(2) increased migration and intercellular adhesion molecule 1 (ICAM)-1 expression in human oral cancer cells. Using pharmacological inhibitors, activators, and genetic inhibition of EP receptors, we discovered that the EP1 receptor, but not other PGE receptors, is involved in PGE(2)-mediated cell migration and ICAM-1 expression. PGE(2)-mediated migration and ICAM-1 up-regulation were attenuated by inhibitors of protein kinase C (PKC)δ, and c-Src. Activation of the PKCδ, c-Src, and AP-1 signaling pathway occurred after PGE(2) treatment. PGE(2)-induced expression of ICAM-1 and migration activity were inhibited by a specific inhibitor, siRNA, and mutants of PKCδ, c-Src, and AP-1. In addition, migration-prone sublines demonstrated that cells with increased migration ability had higher expression of COX-2 and ICAM-1. Taken together, these results indicate that the PGE(2) and EP1 interaction enhanced migration of oral cancer cells through an increase in ICAM-1 production.
    URI: http://dx.doi.org/10.1074/jbc.M110.108183
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/15777
    Relation: J Biol Chem. 2010 Sep 24;285(39):29808-16
    Appears in Collections:[牙醫學系暨碩士班] 期刊論文

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