首页> 外文期刊>Cellular oncology >The shunting of arachidonic acid metabolism to 5-lipoxygenase and cytochrome p450 epoxygenase antagonizes the anti-cancer effect of cyclooxygenase-2 inhibition in head and neck cancer cells.
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The shunting of arachidonic acid metabolism to 5-lipoxygenase and cytochrome p450 epoxygenase antagonizes the anti-cancer effect of cyclooxygenase-2 inhibition in head and neck cancer cells.

机译:花生四烯酸代谢与5-脂氧合酶和细胞色素p450环氧合酶的分流可拮抗环氧化酶-2抑制在头颈部癌细胞中的抗癌作用。

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摘要

It has recently been found that 5-lipoxygenase (5-LO) and cytochrome P450-2J2 (CYP2J2), molecules capable of arachidonic acid (AA) metabolism, might promote cancer cell viability through several mechanisms similar to those of cyclooxygenase-2 (COX-2). We found that not only COX-2 expression, but also the expression of 5-LO and CYP2J2 is up-regulated in head and neck squamous cell carcinoma (HNSCC) cell lines. From these observations, we hypothesized that AA metabolism by 5-LO and/or CYP2J2 may lower the efficacy of anti-cancer effect by COX-2 inhibition.Although COX-2 was highly expressed in all cell lines tested, COX-2-specific inhibition showed little growth-inhibitory effect in some cell lines. Inhibition of COX-2 resulted in increased production of LTB(4) and 14-15-DHET/EET, metabolites of 5-LO and CYP2J2, respectively. Combined knock-down of COX-2 and 5-LO or CYP2J2 by siRNA results in a decrease in cell proliferation and VEGF production. Furthermore, these results are dependent on 5-LO and CYP2J2 expression in cells.Therefore, combined inhibition of COX-2 and 5-LO or CYP2J2 may be one way to overcome low efficacy of single inhibition of COX-2 in cancer cells. In addition, combined therapies should be chosen based on the expression of members of other AA metabolism pathways.
机译:最近发现,能够进行花生四烯酸(AA)代谢的分子5-脂氧合酶(5-LO)和细胞色素P450-2J2(CYP2J2)可能通过类似于环氧合酶-2(COX)的几种机制促进癌细胞的生存能力。 -2)。我们发现在头颈部鳞状细胞癌(HNSCC)细胞系中不仅COX-2表达而且5-LO和CYP2J2表达上调。根据这些观察结果,我们假设5-LO和/或CYP2J2的AA代谢可能会降低COX-2抑制作用的抗癌效果。尽管在所有测试的细胞系中,COX-2均高表达,但COX-2特异性抑制作用在某些细胞系中几乎没有生长抑制作用。抑制COX-2分别导致LTB(4)和14-15-DHET / EET,5-LO和CYP2J2代谢产物的产生增加。 siRNA联合敲低COX-2和5-LO或CYP2J2会导致细胞增殖和VEGF生成减少。此外,这些结果取决于细胞中5-LO和CYP2J2的表达,因此,联合抑制COX-2和5-LO或CYP2J2可能是克服单一抑制COX-2在癌细胞中低效的方法。此外,应根据其他AA代谢途径成员的表达选择联合疗法。

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