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吲哚美辛可降低HCA - 7人结肠癌细胞中花生四烯酸的摄取。

Indomethacin decreases arachidonic acid uptake in HCA-7 human colon cancer cells.

作者信息

Orido Takashi, Fujino Hiromichi, Hasegawa Yuta, Toyomura Kaori, Kawashima Tatsuo, Murayama Toshihiko

机构信息

Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Japan.

出版信息

J Pharmacol Sci. 2008 Nov;108(3):389-92. doi: 10.1254/jphs.08167sc. Epub 2008 Nov 6.

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) reduce the incidence of colorectal cancer. However, evidence is accumulating that NSAIDs have anti-cancer effects in addition to inhibiting cyclooxygenase (COX)-mediated prostanoid biosynthesis. We now show that indomethacin, a popular NSAID, significantly reduced the [3H]-arachidonic acid uptake in HCA-7 human colon cancer cells. Interestingly, no decrease in the uptake of [3H]-arachidonic acid occurred when the cells were treated with aspirin, diclofenac, and sulindac even though the concentrations of these NSAIDs were high enough to inhibit COX-2 activity. These findings suggest that indomethacin has a novel anti-cancer effect that may be independent of COX-2 inhibition.

摘要

非甾体抗炎药(NSAIDs)可降低结直肠癌的发病率。然而,越来越多的证据表明,NSAIDs除了抑制环氧化酶(COX)介导的前列腺素生物合成外,还具有抗癌作用。我们现在发现,一种常用的NSAIDs——吲哚美辛,可显著降低HCA-7人结肠癌细胞中[3H] - 花生四烯酸的摄取。有趣的是,当用阿司匹林、双氯芬酸和舒林酸处理细胞时,[3H] - 花生四烯酸的摄取并未减少,尽管这些NSAIDs的浓度足以抑制COX-2活性。这些发现表明,吲哚美辛具有一种可能独立于COX-2抑制作用的新型抗癌作用。

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