中山醫學大學機構典藏 CSMUIR:Item 310902500/15733
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    題名: Melatonin inhibits TPA-induced oral cancer cell migration by suppressing matrix metalloproteinase-9 activation through the histone acetylation.
    作者: CM, Yeh
    CW, Lin
    JS, Yang
    WE, Yang
    SC, Su
    SF, Yang
    貢獻者: 中山醫大口腔科學研究所
    關鍵詞: CREBBP;EP300;MMP;melatonin;oral cancer
    日期: 2016-04-19
    上傳時間: 2016-08-11T03:57:28Z (UTC)
    ISSN: 1949-2553
    摘要: Melatonin exerts antimetastatic effects on liver and breast cancer and also inhibits matrix metalloproteinase (MMP) activity. However, the detailed impacts and underlying mechanisms of melatonin on oral cancer cell metastasis are still unclear. This study showed that melatonin attenuated the 12-O-tetradecanoylphorbol-13-acetate-induced migration of oral cancer cell lines, HSC-3 and OECM-1. Zymography, quantitative real-time PCR, and Western blotting analyses revealed that melatonin lessened MMP-9 enzyme activity as well as the expression of MMP-9 mRNA and protein. Furthermore, melatonin suppressed the phosphorylation of the ERK1/2 signalling pathway, which dampened MMP-9 gene transcription by affecting the expression of transcriptional coactivators, such as CREB-binding protein (CREBBP) and E1A binding protein p300 (EP300), and decreasing histone acetylation in HSC-3 and OECM-1 cells. Examinations on clinical samples exhibited that MMP-9, CREBBP, and EP300 were significantly increased in oral cancer tissues. Moreover, the relative level of CREBBP was positively correlated with the expression of MMP-9 and EP300. In conclusion, we demonstrated that melatonin inhibits the motility of HSC-3 and OECM-1 cells in vitro through a molecular mechanism that involves attenuation of MMP-9 expression and activity mediated by decreased histone acetylation.
    URI: http://dx.doi.org/10.18632/oncotarget.8009
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/15733
    關聯: Oncotarget. 2016 Apr 19;7(16):21952-67
    顯示於類別:[牙醫學系暨碩士班] 期刊論文

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