Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/33676
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18268/20495 (89%)
Visitors : 9087874      Online Users : 1024
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    CNU IR > Pharmacy and Science > 2017 >  Item 310902800/33676


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/33676


    题名: Secondary metabolites of Neosartorya fischeri inhibited fibroblast-mediated tumorigenensis in triple-negative breast cancer
    作者: 張怡蓉
    黃靖雯
    謝正明
    梁雅婷
    李冠漢
    王嘉駿
    田孝威
    贡献者: 生物科技系
    藥學系
    新藥創建研究中心
    美國南加州大學 藥理暨藥物科學系)
    美國南加州大學 化學系
    关键词: Triple-negative breast cancer
    fibroblast
    Neosartorya fischeri
    secondary metabolite
    日期: 2017
    上传时间: 2022-01-25 15:07:11 (UTC+8)
    摘要: Triple-negative breast cancer (TNBC), which is tested negative for estrogen receptor,progesterone receptor and HER2/neu receptor, is an aggressive histological subtype of breastcancer with limited choice of treatments. Epidermal growth factor receptor (EGFR) tyrosinekinase inhibitors (TKIs) have been studied to inhibit proliferation of TBNC, however, theylacked efficacy in clinical treatment. This may be due to cross-talk between cancer cells andneighboring stromal cells. For example, hepatocyte growth factor (HGF) secreted bycancer-associated fibroblasts has been shown to bind to a Met receptor and reduce efficiencyof TKIs in TNBC, indicating that microenvironment affected development of cancer cells. Tosurvey the effective TNBC inhibitors, we established a soft agar colony formation system forbreast cancer MDA-MB-468 cells with co-culture of fibroblasts. Neosartorya fischeri extractswere tested for their inhibitory activity on TNBC by applying to this system. The resultsshowed that some secondary metabolites of Neosartorya fischeri inhibitedfibroblast-mediated colony formation of MDA-MB-468 cells. One of these metabolitesexhibited inhibitory effect on phosphorylation of EGFR and Met, which offered the potentialas a chemotherapeutic agent for TNBC.
    關聯: 2017 第十一屆嘉南藥理大學藥理學院師生研究成果發表會,起迄日:2017/05/02-2017/05/04
    显示于类别:[Pharmacy and Science] 2017
    [Dept. of Pharmacy] Proceedings
    [Dept. of Biotechnology (including master's program)] Proceedings

    文件中的档案:

    档案 大小格式浏览次数
    F03.pdf669KbAdobe PDF176检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈