Sanghani Sonal P, Quinney Sara K, Fredenburg Tyler B, Davis Wilhelmina I, Murry Daryl J, Bosron William F
Biotechnology Research and Training Center, Indiana University School of Medicine, 1345 W. 16th Street, Room L3-304, Indianapolis, IN 46202, USA.
Drug Metab Dispos. 2004 May;32(5):505-11. doi: 10.1124/dmd.32.5.505.
Carboxylesterases metabolize ester, thioester, carbamate, and amide compounds to more soluble acid, alcohol, and amine products. They belong to a multigene family with about 50% sequence identity between classes. CES1A1 and CES2 are the most studied human isoenzymes from class 1 and 2, respectively. In this study, we report the cloning and expression of a new human isoenzyme, CES3, that belongs to class 3. The purified recombinant CES3 protein has carboxylesterase activity. Carboxylesterases metabolize the carbamate prodrug 7-ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin (CPT-11; irinotecan) to its active metabolite 7-ethyl-10-hydroxycamptothecin (SN-38), a potent topoisomerase I inhibitor. CYP3A4 oxidizes CPT-11 to two major oxidative metabolites, 7-ethyl-10-[4-N-(5-aminopentanoic acid)-1-piperidino] carbonyloxycamptothecin (APC) and 7-ethyl-10-[4-(1-piperidino)-1-amino]-carbonyloxycamptothecin (NPC). In this study, we investigate whether these oxidative metabolites, NPC and APC, can be metabolized to SN-38 by purified human carboxylesterases, CES1A1, CES2, and CES3. We find that CPT-11, APC, and NPC can all be metabolized by carboxylesterases to SN-38. CES2 has the highest catalytic activity of 0.012 min(-1) microM(-1) among the three carboxylesterases studied for hydrolysis of CPT-11. NPC was an equally good substrate of CES2 in comparison to CPT-11, with a catalytic efficiency of 0.005 min(-1) microM(-1). APC was a very poor substrate for all three isoenzymes, exhibiting a catalytic activity of 0.015 x 10(-3) min(-1) microM(-1) for CES2. Catalytic efficiency of CES3 for CPT-11 hydrolysis was 20- to 2000-fold less than that of CES1A1 and CES2. The relative activity of the three isoenzymes was CES2 > CES1A1 >> CES3, for all three substrates.
羧酸酯酶可将酯、硫酯、氨基甲酸酯和酰胺类化合物代谢为更易溶解的酸、醇和胺类产物。它们属于一个多基因家族,不同类别之间的序列同一性约为50%。CES1A1和CES2分别是来自第1类和第2类中研究最多的人类同工酶。在本研究中,我们报道了一种属于第3类的新型人类同工酶CES3的克隆和表达。纯化的重组CES3蛋白具有羧酸酯酶活性。羧酸酯酶可将氨基甲酸酯前药7-乙基-10-[4-(1-哌啶基)-1-哌啶基]羰基氧基喜树碱(CPT-11;伊立替康)代谢为其活性代谢物7-乙基-10-羟基喜树碱(SN-38),一种强效的拓扑异构酶I抑制剂。CYP3A4将CPT-11氧化为两种主要的氧化代谢物,7-乙基-10-[4-N-(5-氨基戊酸)-1-哌啶基]羰基氧基喜树碱(APC)和7-乙基-10-[4-(1-哌啶基)-1-氨基]-羰基氧基喜树碱(NPC)。在本研究中,我们研究了这些氧化代谢物NPC和APC是否能被纯化的人类羧酸酯酶CES1A1、CES2和CES3代谢为SN-38。我们发现CPT-11、APC和NPC都能被羧酸酯酶代谢为SN-38。在所研究的三种用于水解CPT-11的羧酸酯酶中,CES2具有最高的催化活性,为0.012 min(-1) microM(-1)。与CPT-11相比,NPC是CES2同样良好的底物,催化效率为0.005 min(-1) microM(-1)。APC是所有三种同工酶的非常差的底物,对CES2表现出0.015×10(-3) min(-1) microM(-1)的催化活性。CES3对CPT-11水解的催化效率比对CES1A1和CES2低20至2000倍。对于所有三种底物,三种同工酶的相对活性为CES2 > CES1A1 >> CES3。