Glucuronidation of estrone and 16α-hydroxyestrone by human UGT enzymes: The key roles of UGT1A10 and UGT2B7

被引:29
作者
Kallionpaa, Roope A. [1 ]
Jarvinen, Erkka [1 ]
Finel, Moshe [1 ]
机构
[1] Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, Helsinki 00014, Finland
基金
芬兰科学院;
关键词
Estrone glucuronidation; UGT1A10; 16 alpha-Hydroxyestrone conjugation; UGT2B7; Extrahepatic glucuronidation; Intestine microsomes; HUMAN UDP-GLUCURONOSYLTRANSFERASE; BREAST-CANCER; METABOLITES; ESTRADIOL; EXPRESSION; BINDING; CLONING;
D O I
10.1016/j.jsbmb.2015.07.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The glucuronidation of estrone and 16 alpha-hydroxyestrone by recombinant human UDP-glucuronosyl-transferase enzymes (UGTs) of subfamilies 1A, 2A and 2B was studied. Microsomes from human liver and small intestine were also tested for the glucuronidation of these two estrogens. The results revealed that UGT1A10 is by far the most active enzyme in estrone glucuronidation. UGT1A10 also exhibited high rate of 16 alpha-hydroxyestrone conjugation at the 3-OH, whereas UGT2B7 catalyzed its glucuronidation at high rates at the 16-OH. Human liver microsomes exhibited high rates of 16 alpha-hydroxyestrone-16-glucuronide formation, but very low formation rates of either 16 alpha-hydroxyestrone-3-glucuronide or estrone glucuronide. On the other hand, human intestine microsomes catalyzed the formation of all these 3 different glucuronides at high rates. Kinetic analyses revealed very low K-m value for 16 alpha-hydroxyestrone glucuronidation by UGT2B7, below 4 mu M, suggesting higher affinity than commonly found among UGTs and their substrates. In further studies with UGT1A10, mutant F93G exhibited increased glucuronidation rates of 16 alpha-hydroxyestrone, but not estrone, whereas mutations in F90 did not reveal any activity with either estrogen. Taken together, the results of this study significantly expand our understanding on the metabolism of estrogens and their interactions with the human UGTs. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 111
页数:8
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