Curcumin inhibits cyclooxygenase-2 transcription in bile acid- and phorbol ester-treated human gastrointestinal epithelial cells

被引:230
作者
Zhang, F
Altorki, NK
Mestre, JR
Subbaramaiah, K
Dannenberg, AJ
机构
[1] New York Presbyterian Hosp, Div Gastroenterol & Hepatol, New York, NY 10021 USA
[2] New York Presbyterian Hosp, Dept Cardiothorac Surg, New York, NY 10021 USA
[3] New York Presbyterian Hosp, Dept Med, New York, NY 10021 USA
[4] New York Presbyterian Hosp, Dept Surg, New York, NY 10021 USA
[5] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Surg, Head & Neck Serv, New York, NY 10021 USA
[7] Anne Fisher Nutr Ctr & Strang Canc Prevent Ctr, New York, NY 10021 USA
关键词
D O I
10.1093/carcin/20.3.445
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated whether curcumin, a chemopreventive agent, inhibited chenodeoxycholate (CD)- or phorbol ester (PMA)-mediated induction of cyclooxygenase-2 (COX-2) in several gastrointestinal cell lines (SK-GT-4, SCC450, IEC-18 and HCA-7). Treatment with curcumin suppressed CD- and PMA-mediated induction of COX-2 protein and synthesis of prostaglandin E-2. Curcumin also suppressed the induction of COX-2 mRNA by CD and PMA. Nuclear run-offs revealed increased rates of COX-2 transcription after treatment with CD or PMA and these effects were inhibited by curcumin. Treatment with CD or PMA increased binding of AP-1 to DNA, This effect was also blocked by curcumin. In addition to the above effects on gene expression, we found that curcumin directly inhibited the activity of COX-2. These data provide new insights into the anticancer properties of curcumin.
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页码:445 / 451
页数:7
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