ASIA unversity:Item 310904400/25218
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    题名: Endothelin-1 enhances cell migration through COX-2 up-regulation in human chondrosarcoma
    作者: Wu, Min Huan;Chen, Li-Mien;Hsu, His-Hsien;James, A.Lin;Lin, Yueh-Min;蔡輔仁;Tsai, Fuu-Jen;蔡長海;黃志揚;HUANG, CHIH-YANG;Tang, Chih-Hsin
    贡献者: 生物科技學系
    关键词: Endothelin-1 (ET-1);Metastasis;Chondrosarcoma;Cyclooxygenase (COX)-2;Activator protein-1 (AP-1)
    日期: 2013
    上传时间: 2013-07-11 13:55:51 (UTC+8)
    摘要: Background
    Chondrosarcoma is a type of highly malignant tumor with a potent capacity of local invasion and distant metastasis. The effect of endothelin-1 (ET-1) on migration activity in human chondrosarcoma cells is not clearly understood. Here, we found that ET-1 increased the migration and expression of cyclooxygenase (COX)-2 in human chondrosarcoma cells.

    Methods
    ET-1-mediated COX-2 expression was assessed by qPCR and Western blot analysis. The mechanisms of action of ET-1 in different signaling pathways were studied using Western blotting. Knockdown of proteins was achieved by transfection with siRNA. Chromatin immunoprecipitation assays were used to study in vivo binding of c-Jun to the COX-2 promoter.

    Results
    Human chondrosarcoma tissues had significant expression levels of ET-1 and COX-2, which were higher than that in normal cartilage. Exogenous ET-1 increased cell migration and the expression of COX-2. In addition, COX-2 protein levels and cell migration ability were abolished by ET receptor antagonists. Activation of the mitogen-activated protein kinase (MAPK) and activator protein-1 (AP-1) pathways after ET-1 treatment was demonstrated, and ET-1-induced COX-2 expression and cell migration activity were inhibited by the specific inhibitor and mutant of MAPK and AP-1 cascades. ET-1 increased the binding of c-Jun to the AP-1 element on the COX-2 promoter. Furthermore, knockdown of ET-1 decreased cell metastasis in vitro and in vivo.

    Conclusions
    Our results indicated that ET-1 enhances the cell migration of chondrosarcoma by increasing COX-2 expression through the ET receptors, MAPK, and AP-1 signal transduction pathway.

    General significance
    We link high ET-1 and COX-2 expression to chondrosarcoma.
    關聯: BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS,1830(6).3355–3364.
    显示于类别:[生物科技學系] 期刊論文

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