首页> 外文期刊>European Journal of Pharmacology: An International Journal >Indomethacin antagonizes EP 2 prostanoid receptor activation in LS174T human colon cancer cells
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Indomethacin antagonizes EP 2 prostanoid receptor activation in LS174T human colon cancer cells

机译:吲哚美辛拮抗LS174T人结肠癌细胞中EP 2前列腺素受体的活化

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摘要

Increases in the level of cyclooxygenase (COX)-2 and prostanoids such as prostaglandin E 2 (PGE 2) are considered biomarkers of colorectal cancer. Therefore, non-steroidal anti-inflammatory drugs (NSAID) have been used to reduce the risk of cancer development by reducing prostanoid biosynthesis as COX inhibitors. Along with their activity as COX inhibitors, NSAID have been reported to have other effects. One major NSAID, indomethacin, has been shown to have several effects independent of COX inhibition. To further examine the COX-inhibition-independent effects of indomethacin on colorectal cancer, we used human colon cancer LS174T cells, known to have express little COX-2 and have no detectable PGE 2 production. Here we show that indomethacin has a potential antagonizing effect on human EP 2 receptors. We believe this study raises the reasons to use indomethacin as a lead-compound for setting up another EP 2 receptor-specific antagonist as a relatively cost-efficient strategy for anti-cancer medication in the future.
机译:环氧合酶(COX)-2和前列腺素(例如前列腺素E 2(PGE 2))水平的升高被认为是结直肠癌的生物标志物。因此,非甾体类抗炎药(NSAID)已用于通过减少前列腺素类生物合成作为COX抑制剂来降低癌症发展的风险。据报道,NSAID及其作为COX抑制剂的活性还具有其他作用。一种主要的NSAID消炎痛已显示出多种独立于COX抑制作用的作用。为了进一步检查吲哚美辛对结肠直肠癌的COX抑制非依赖性作用,我们使用了人类结肠癌LS174T细胞,该细胞已知仅表达少量COX-2并且没有可检测的PGE 2产生。在这里,我们显示消炎痛对人的EP 2受体具有潜在的拮抗作用。我们认为,这项研究提出了使用吲哚美辛作为先导化合物建立另一种EP 2受体特异性拮抗剂的理由,作为未来抗癌药物的相对具有成本效益的策略。

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