國家衛生研究院 NHRI:Item 3990099045/11727
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 12145/12927 (94%)
造訪人次 : 925125      線上人數 : 896
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    主頁登入上傳說明關於NHRI管理 到手機版
    請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/11727


    題名: The anti-proliferative effect of CAPE on docetaxel-resistant prostate cancer cells
    作者: Fu, YK;Tseng, JC;Huang, SH;Lin, CY;Chuu, CP
    貢獻者: Institute of Cellular and Systems Medicine
    摘要: The majority of patients with prostate cancer (PCa) receiving androgen ablation therapy will relapse castration-resistant prostate cancer (CRPC) within 1-3 years. Docetaxel is a FDA-approved chemotherapeutic drug for CRPC, however, PCa patient receiving docetaxel develop drug-resistant phenotype after a few months. Caffeic acid phenethyl ester (CAPE) is the main component for honey bee propolis. We previously showed that CAPE can suppresses growth of PCa tumors. In this study, we explored if CAPE can suppress docetaxel-resistant PCa cells. We observed that CAPE dose-dependently suppressed proliferation of docetaxel-resistant PC-3 cells, as well as growth of this docetaxel-resistant PC-3 xenograt in nude mice. We found that CAPE treatment promoted apoptosis-related proteins and thus induced apoptosis in docetaxel-resistant PC-3 cells. In conclusion, CAPE is an potential treatment for docetaxel-resistant PCa.
    日期: 2018-12
    關聯: Cancer Science. 2018 Dec;109(Suppl. 2):574.
    Link to: https://doi.org/10.1111/cas.13904
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1347-9032&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000453773602350
    顯示於類別:[褚志斌] 會議論文/會議摘要

    文件中的檔案:

    檔案 大小格式瀏覽次數
    ISI000453773602350.pdf33KbAdobe PDF259檢視/開啟


    在NHRI中所有的資料項目都受到原著作權保護.

    TAIR相關文章

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