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Inhibition of Proliferation and Induction of Differentiation of Human and Mouse Myeloid Leukemia Cells by New Ethyleneglycol‐type Nonphosphorus Alkyl Ether Lipids

机译:新型乙二醇型非磷烷基醚脂质抑制人和小鼠骨髓白血病细胞的增殖并诱导分化

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摘要

A variety of ethyleneglycol‐type nonphosphorus alkyl ether lipids, ether derivatives of diethylene‐glycol in which the two hydroxyl groups were substituted with long chain alkyl and quaternary ammonioalkyl groups, were synthesized and their effects on proliferation and differentiation of cultured human (HL‐60) and mouse (M1) myeloid leukemia cells were studied. Incubation with these compounds inhibited the cellular proliferation, and the cells differentiated into morphologically and functionally mature granulocytes. Of the compounds tested, 1‐[2‐[2‐(octadecyloxy)ethoxy]ethoxy]‐butylpyridinium mesylate (EG‐6) was the most effective in inducing differentiation of HL‐60 cells. Almost maximal induction of differentiation and inhibition of growth of HL‐60 cells on day 6 were observed when the cells were treated with EG‐6 for 1 day and then cultured without EG‐6 for a further 5 days. The inhibitory effect of EG‐6 on the leukemic cells was over 100 times more than that of 2‐[2‐(dodecyloxy)ethoxy]ethyl 2‐pyridinioethyl phosphate, a potent antileukemic ether phospholipid.
机译:合成了多种乙二醇型非磷烷基醚脂质,即其中两个羟基被长链烷基和季铵烷基取代的二甘醇的醚衍生物,它们对培养的人的增殖和分化具有影响(HL-60 )和小鼠(M1)骨髓白血病细胞进行了研究。与这些化合物一起孵育可抑制细胞增殖,并使细胞分化为形态和功能成熟的粒细胞。在测试的化合物中,1- [2- [2-(十八烷基氧基)乙氧基]乙氧基]-甲基吡啶鎓吡啶鎓(EG-6)在诱导HL-60细胞分化方面最有效。当用EG-6处理细胞1天,然后再不使用EG-6培养5天时,在第6天观察到几乎最大程度的诱导HL-60细胞分化和抑制生长。 EG-6对白血病细胞的抑制作用是磷酸2- [2-(十二烷基氧基)乙氧基]乙基2-吡啶碘乙基磷酸盐的100倍以上,后者是一种有效的抗白血病醚磷脂。

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