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Synthesis and Biological Activity of Anticancer Ether Lipids That Are Specifically Released by Phospholipase A_2 in Tumor Tissue

机译:磷脂酶A_2在肿瘤组织中特异性释放的抗癌醚脂质的合成及生物学活性

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摘要

The clinical use of anticancer lipids is severely limited by their ability to cause lysis of red blood cells prohibiting intravenous injection.Novel delivery systems are therefore required in order to develop anticancer ether lipids(AELs)into clinically useful anticancer drugs.In a recent article(J.Med.Chem.2004,47,1694)we showed that it is possible to construct liposome systems composed of masked AELs that are activated by secretory phospholipase A_2 in cancerous tissue.We present here the synthesis of six AELs and evaluate the biological activity of these bioactive lipids.The synthesized AEL 1-6 were tested against three different cancer cell lines.It was found that the stereochemistry of the glycerol headgroup in AEL-2 and 3 has a dramatic effect on the cytotoxicity of the lipids.AEL 1-4 were furthermore evaluated for their ability to prevent phosphorylation of the apoptosis regulating kinase Akt,and a correlation was found between their cytotoxic activity and their ability to inhibit Akt phosphorylation.
机译:抗癌脂质的临床应用受到严重限制,因为它们导致红细胞裂解而无法静脉注射,因此需要新颖的递送系统才能将抗癌醚脂质(AELs)研发成临床上有用的抗癌药物。 J.Med.Chem.2004,47,1694)研究表明,有可能构建由被掩盖的AEL组成的脂质体系统,该脂质系统被癌组织中的分泌性磷脂酶A_2激活。我们在此介绍了六种AEL的合成并评估了其生物学活性对三种不同的癌细胞系测试了合成的AEL 1-6,发现AEL-2和3中甘油首基的立体化学对脂质的细胞毒性有显着影响.AEL 1-此外,还评估了4种细胞预防凋亡调节激酶Akt磷酸化的能力,并发现它们的细胞毒活性与抑制能力之间存在相关性。它的Akt磷酸化。

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