Balzarini J, Karlsson A, Wang L, Bohman C, Horská K, Votruba I, Fridland A, Van Aerschot A, Herdewijn P, De Clercq E
Rega Institute for Medical Research, Katholieke Universiteit Lewen, Belgium.
J Biol Chem. 1993 Nov 25;268(33):24591-8.
EICAR (5-ethynyl-1-beta-D-ribofuranosylimidazole-4-carboxamide) is a cytostatic agent that inhibits murine leukemia L1210 and human lymphocyte CEM cells at a 50% inhibitory concentration of 0.80-1.4 microM, respectively. EICAR causes a rapid and marked inhibition of inosinate (IMP) dehydrogenase (EC 1.1.1.205) activity in intact L1210 and CEM cells reflected by a concentration-dependent accumulation of IMP and depletion of GTP and dGTP levels. EICAR 5'-monophosphate is a potent inhibitor of purified L1210 cell IMP dehydrogenase (Ki/Km 0.06). Inhibition of IMP dehydrogenase by EICAR 5'-monophosphate is competitive with respect to IMP. L1210 cells that were selected for resistance to the cytostatic action of EICAR proved to be adenosine kinase-deficient. Also, studies with other mutant L1210 and CEM cell lines revealed that adenosine kinase, as well as an alternative pathway, may be responsible for the conversion of EICAR to its 5'-monophosphate. Purified 2'-deoxycytidine kinase, 2'-deoxyguanosine kinase, cytosolic 5'-nucleotidase, and nicotinamide dinucleotide (NAD) pyrophosphorylase do not seem to be markedly involved in the metabolism of EICAR.
EICAR(5-乙炔基-1-β-D-呋喃核糖基咪唑-4-甲酰胺)是一种细胞生长抑制剂,分别在0.80 - 1.4微摩尔的50%抑制浓度下抑制小鼠白血病L1210细胞和人淋巴细胞CEM细胞。EICAR导致完整的L1210细胞和CEM细胞中的次黄苷酸(IMP)脱氢酶(EC 1.1.1.205)活性迅速且显著受到抑制,这表现为IMP的浓度依赖性积累以及GTP和dGTP水平的消耗。EICAR 5'-单磷酸是纯化的L1210细胞IMP脱氢酶的强效抑制剂(Ki/Km为0.06)。EICAR