English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1498366      線上人數 : 361
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/310903500/2921


    題名: The effect of paclitaxel on 2-aminofluorene-DNA adducts formation and arylamine N-acetyltransferase activity and gene expression in human lung tumor cells (A549).
    作者: 夏德椿(Hsia,Te-Chun);鍾景光(Chung, Jing-Gung)*;(Lu, H.F.);何恆堅;(Yang, C.C.);(Lu, K.H.);洪啟賦
    貢獻者: 中醫學院中醫學系學士班中醫內科學科;中國附醫高壓氧治療中心
    關鍵詞: Curcumin;DNA adduct formation;N-Acetyltransferase;2-Aminofluorene
    日期: 2002-05
    上傳時間: 2009-08-20 17:57:42 (UTC+8)
    摘要: It is well known that N-acetyltransferase (NAT)plays an important role in the arylamine metabolism. We analysed the response
    of A549 human lung cancer cells for N-acetylation of 2-aminofluorene (AF)to curcumin. After curcumin treatment, the NAT
    activity was examined by HPLC, AF-DNA adduct formation was examined by HPLC, and NAT gene expression by polymerase
    chain reaction were detected. The NAT activity in the human A549 cells and cytosols was suppressed by curcumin in a dosedependent
    manner. The results also demonstrated that gene expression (NAT1 mRNA)in human lung A549 tumor cells was inhibited and decreased by curcumin. After the incubation of human lung A549 tumor cells with AF with or without curcumin cotreatment, the cells were recovered and DNA was prepared and hydrolyzed to nucleotides. The adducted nucleotides were extracted into butanol and analyzation of AF-DNA adducts was done by HPLC. The results also demonstrated that curcumin decreases AF-DNA adduct formation in the human lung A549 tumor cells.
    關聯: FOOD AND CHEMICAL TOXICOLOGY 40(5):697~703
    顯示於類別:[中醫學系暨碩博班] 期刊論文

    文件中的檔案:

    檔案 大小格式瀏覽次數
    0KbUnknown407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