Meiho University Institutional Repository:Item 987654321/1691
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    题名: Proteomic investigation of anti-tumor activities exerted by sinularin against A2058 melanoma cells
    作者: Su, Tzu-Rong
    Lin, Jen-Jie
    Chiu, Chien-Chih
    Chen, Jeff Yi-Fu
    Su, Jui-Hsin
    Cheng, Zhi-Jiao
    Hwang, Wen-Ing
    Huang, Han Hsiang
    Wu, Yu-Jen
    贡献者: 健康暨護理學院
    关键词: Melanoma cells;Proteomic analysis;Sinularin
    日期: 2011
    上传时间: 2012-09-03T01:15:02Z (UTC)
    摘要: The extracts from soft corals have been increasingly investigated for biomedical and therapeutic
    purposes. The aim of this study is to examine and analyze the anti-tumor effects of
    the genus Sinularia extract sinularin on A2058 melanoma cells using MTT assay, cell migration
    assay, wound healing assay, flow cytometric analysis, and proteomic analysis. Sinularin
    dose-dependently (1–5 g/mL) inhibited melanoma cell proliferation while the treatment
    at identical concentrations suppressed cell migration. Sinularin dose-dependently
    enhanced apoptotic melanoma cells and caused tumor cell accumulation at G2/M phase,
    indicating that sinularin exerts apoptosis-induced and cell cycle-delayed activities in A2058
    melanoma cells.Comparative proteomic analysiswas conducted to investigate the effects of
    sinularin at the molecular level by comparison between the protein profiling ofmelanoma
    cells treated with sinularin and without the treatment. Thirty-five differential proteins (13
    upregulated and 22 downregulated) concerning the treatment were identified by liquid
    chromatography-tandem mass spectrometry. Proteomic data and Western blot displayed
    the levels of several tumor inhibitory or apoptosis-associated proteins including annexin
    A1, voltage-dependent anion-selective channel protein 1 and prohibitin (upregulated),
    heat shock protein 60, heat shock protein beta-1, and peroxiredoxin-2 (downregulated) in
    A2058 melanoma cells exposed to sinularin. Increased expression of p53, cleaved-caspase-
    3, cleaved-caspase-8, cleaved-caspase-9, p21, and Bax and decreased expression of Bcl-2 in
    sinularin-treated melanoma cells suggest that the anti-tumor activities of sinularin against
    melanoma cells are particularly correlated with these pro-apoptotic factors. These data
    provide important information for the mechanisms of anti-tumor effects of sinularin on
    melanoma cells and may be helpful for drug development and progression monitoring of
    human melanoma.
    显示于类别:[美容系] 研究計畫

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