English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1994260      線上人數 : 374
RC Version 7.0 © 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CMUR管理 到手機版
    請使用永久網址來引用或連結此文件: http://ir.cmu.edu.tw/ir/handle/310903500/24106


    題名:   酸類緣物對於人類前骨髓性血癌細胞 ( HL-60 cells );Effect of Indole-3-acetic acid Analogs on Differentiation
    作者: 陳俊仁;Chen Chun Jen
    貢獻者: 中國醫藥學院藥物化學研究所
    關鍵詞: 細胞分化劑;-3-醋酸類緣物;全反式維甲酸;人類前骨髓性白血病;細胞週期;cell differentiation agents;Indole-3-acetic acid ( IAA ) analogs;all-trans retinoic acid ( ATRA );acute promyelocytic leukemia ( APL );cell cycle;HL-60 cell;NBT
    日期: 1990
    上傳時間: 2009-12-03 09:30:38 (UTC+8)
    摘要: 為了尋求新型的細胞分化劑,著者針對一系列??-3-醋酸 ( IAA ) 類緣物進行分化作用與抑制增殖作用之篩選工作。發現化合物IAA-Ile及IAA-Phe其二者對促進全反式維甲酸分化活性之效果最為顯著。於是進一步地以其對HL-60細胞週期之影響及細胞表面抗原表現來探討其初步作用機轉。 當化合物IAA-Ile及IAA-Phe與全反式維甲酸併用時,其對細胞週期及細胞表面抗原表現影響的結果顯示與全反式維甲酸於誘導細胞分化時產生的結果相似。綜合本研究結果:化合物IAA-Ile及IAA-Phe併用全反式維甲酸使用於人類前骨髓性白血病的分化療法上應有不錯的助益。; In order to develop the novel cell differentiation agents, a series of Indole-3-acetic acid ( IAA ) analogs were screened for their differentiation and antiproliferation activities of HL-60 cells. Compounds, IAA-Ile and IAA-Phe were found to be the most effective to potentiate the induction of differentiation by all-trans retinoic acid ( ATRA ). Therefore the further studies were carried out to evaluate their effects on the cell cycle and cell surface antigen expression of HL-60 cells. When combined with ATRA, compounds IAA-Ile and IAA-Phe were found to affect the cell cycle and cell surface antigen expression in the same manner as ATRA. This finding suggest that IAA-Ile and IAA-Phe when administered together with ATRA, may have beneficial therapeutic effects in the treatment of acute promyelocytic leukemia ( APL ).
    顯示於類別:[藥物化學研究所] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML278檢視/開啟


    在CMUR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