ASIA unversity:Item 310904400/81130
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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/81130


    Title: Naringin suppress chondrosarcoma migration through inhibition vascular adhesion molecule-1 expression by modulating miR-126
    Authors: Tan, Tzu-Wei;Tan, Tzu-Wei;Cho, Ying-Erh;Chou, Ying-Erh;Yan, Wei-Hung;Yang, Wei-Hung;Hs, Chin-Jung;Hsu, Chin-Jung;Fong, Yi-Chin;Fong, Yi-Chin;湯智昕;Chih-Hsin, Tang;*
    Contributors: 生物科技學系
    Keywords: Chondrosarcoma;Migration;Naringin;Vascular cell adhesion molecule-1;miR-126
    Date: 2014-06
    Issue Date: 2014-10-01 08:32:07 (UTC+0)
    Abstract: Chondrosarcoma, a primary malignant bone cancer, has a potent capacity to invade locally and cause distant metastasis, especially to the lungs. Patients diagnosed with it have poor prognosis. Naringin, polymethoxylated flavonoid commonly found in citrus fruits, has anti-oxidant, anti-inflammatory and anti-tumor activity; whether naringin regulates migration of chondrosarcoma is largely unknown. Here we report that naringin does not expedite apoptosis in human chondrosarcoma. By contrast, at noncytotoxic concentrations, naringin suppressed migration and invasion of chondrosarcoma cells. Vascular cell adhesion molecule-1 (VCAM-1) of the immunoglobulin superfamily is linked with metastasis; we found incubation of chondrosarcoma cells with naringin reducing mRNA transcription for, and cell surface expression of, VCAM-1. We also observed that naringin enhancing miR-126 expression, and miR-126 inhibitor reversed the naringin-inhibited cell motility and VCAM-1 expression. Therefore, naringin inhibits migration and invasion of human chondrosarcoma via down-regulation of VCAM-1 by increasing miR-126. Thus, naringin may be a novel anti-migration agent for the treatment of migration in chondrosarcoma.
    Copyright © 2014 Elsevier B.V. All rights reserved.
    Relation: INTERNATIONAL IMMUNOPHARMACOLOGY;22(1):107-14.
    Appears in Collections:[Department of Biotechnology] Journal Article

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