姜黄素
环氧合酶
前列腺素E2
佛波
化学
十四烷基佛波乙酸酯
细胞培养
前列腺素E
生物化学
分子生物学
抗癌原
抄写(语言学)
药理学
生物
体外
蛋白激酶C
生物活性
内分泌学
磷酸化
酶
遗传学
语言学
哲学
作者
Fan Zhang,Nasser K. Altorki,Juan R. Mestre,Kotha Subbaramaiah,Andrew J. Dannenberg
出处
期刊:Carcinogenesis
[Oxford University Press]
日期:1999-03-01
卷期号:20 (3): 445-451
被引量:286
标识
DOI:10.1093/carcin/20.3.445
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 E2. 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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