Bador H, Morelis R, Louisot P
Int J Biochem. 1983;15(9):1137-42. doi: 10.1016/0020-711x(83)90228-8.
Antineoplastic alkyl-lysophospholipids were found to exert a strong inhibitory effect on membranous or solubilized asialomucin-sialyltransferase (CMP-N-acetylneuraminate: D-galactosyl-glycoprotein N-acetylneuraminyltransferase, EC 2.4.99.1) activity. This inhibitory effect was dependent on the presence of the choline moiety in position 3 of the glycerol molecule, as well as on the presence of long ether-linked aliphatic side chain in position 1 and the absence of any large substituent in position 2. As an example, 1-octadecyl-2-O-methyl-glycero-3-phosphorylcholine acted as a mixed-type inhibitor. Such an inhibitory process on sialyltransferase activity might be an additional factor in the tumor cell destructive effect of alkyl-lysophospholipids.
抗肿瘤烷基溶血磷脂被发现对膜结合型或可溶型去唾液酸糖蛋白唾液酸转移酶(CMP-N-乙酰神经氨酸:D-半乳糖基糖蛋白N-乙酰神经氨酸转移酶,EC 2.4.99.1)的活性具有强烈的抑制作用。这种抑制作用取决于甘油分子3位上胆碱部分的存在,以及1位上长链醚连接脂肪族侧链的存在和2位上无任何大的取代基。例如,1-十八烷基-2-O-甲基甘油-3-磷酸胆碱作为混合型抑制剂。对唾液酸转移酶活性的这种抑制过程可能是烷基溶血磷脂对肿瘤细胞破坏作用的一个额外因素。