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Inhibitory effect of isothiocyanate derivant targeting AGPS by computer-aid drug design on proliferation of glioma and hepatic carcinoma cells

机译:计算机辅助药物设计对靶向AGPS的异硫氰酸酯衍生物对神经胶质瘤和肝癌细胞增殖的抑制作用

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摘要

Lipids metabolism was involved in the process of many types of tumor and alkylglycerone phosphate synthase (AGPS) was considered implicated in tumor process. Benzyl isothiocyanate (BITC) showed the inhibitory effect of tumor and AGPS activity, therefore, we screened a group of small molecular compound based on BITC by computer-aid design targeting AGPS and the results showed that the derivants could suppress the proliferation, the expression of tumor related genes such as survivin and Bcl-2, and the level of ether lipids such as lysophosphatidic acid ether (LPAe) and platelet activating factor ether (PAFe); however, the activity of caspase-3/8 was improved in glioma U87MG and hepatic carcinoma HepG2 cells in vitro.
机译:脂质代谢参与多种类型的肿瘤的过程,而烷基甘油磷酸酯合酶(AGPS)被认为与肿瘤过程有关。异硫氰酸苄酯(BITC)表现出对肿瘤和AGPS活性的抑制作用,因此,我们通过针对AGPS的计算机辅助设计筛选了一组基于BITC的小分子化合物,结果表明该衍生物可以抑制增殖,抑制AGPS的表达。肿瘤相关基因,例如survivin和Bcl-2,以及醚脂质的水平,如溶血磷脂酸醚(LPAe)和血小板活化因子醚(PAFe);然而,在神经胶质瘤U87MG和肝癌HepG2细胞中,caspase-3 / 8的活性有所提高。

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