» Articles » PMID: 18480185

Expression of UGT1A and UGT2B MRNA in Human Normal Tissues and Various Cell Lines

Overview
Specialty Pharmacology
Date 2008 May 16
PMID 18480185
Citations 113
Authors
Affiliations
Soon will be listed here.
Abstract

UDP-glucuronosyltransferases (UGTs) are major phase II drug metabolism enzymes that catalyze the glucuronidation of numerous endogenous and exogenous compounds. UGTs are divided into two families, UGT1 and UGT2, based on evolutionary divergence and homology. Nine UGT1A and seven UGT2B functional isoforms have been identified in humans. Glucuronidation occurs mainly in liver but also in various extrahepatic tissues, possibly affecting the pharmacokinetics. In the present study, we comprehensively determined the expression of all functional UGT1A and UGT2B isoforms in normal human tissues including liver, lung, stomach, small intestine, colon, kidney, bladder, adrenal gland, breast, ovary, uterus, and testis by semiquantitative reverse transcription-polymerase chain reaction. In addition, the expressions of these UGTs mRNA in 15 kinds of human tissue-derived cell lines were also analyzed. Many UGT isoforms were abundantly expressed in the liver, gastrointestinal tract, and kidney, supporting previous studies. Interestingly, we found that all UGTs except UGT2B17 were expressed in bladder. In steroid-related tissues, UGTs were expressed in tissue- and isoform-specific manners. Expression profiles in human tissue-derived cell lines were not necessarily consistent with those in corresponding normal tissues. Different expression profiles were observed in distinct cell lines derived from the same organ. The information presented here will be helpful for understanding the glucuronidation in various tissues and for choosing appropriate cell lines for in vitro studies.

Citing Articles

Prediction of SPT-07A Pharmacokinetics in Rats, Dogs, and Humans Using a Physiologically-Based Pharmacokinetic Model and In Vitro Data.

Zhu X, Kong W, Wang Z, Liu X, Liu L Pharmaceutics. 2025; 16(12).

PMID: 39771574 PMC: 11676658. DOI: 10.3390/pharmaceutics16121596.


The Somatic Mutation Landscape of UDP-Glycosyltransferase () Genes in Human Cancers.

Hu D, Marri S, Hulin J, McKinnon R, Mackenzie P, Meech R Cancers (Basel). 2022; 14(22).

PMID: 36428799 PMC: 9688768. DOI: 10.3390/cancers14225708.


Analysis of in vitro and in vivo metabolism of zidovudine and gemfibrozil in trans-chromosomic mouse line expressing human UGT2 enzymes.

Kobayashi K, Deguchi T, Abe S, Kajitani N, Kazuki K, Takehara S Pharmacol Res Perspect. 2022; 10(6):e01030.

PMID: 36424908 PMC: 9692130. DOI: 10.1002/prp2.1030.


Dysregulated hepatic UDP-glucuronosyltransferases and flavonoids glucuronidation in experimental colitis.

Zeng W, Liu X, Wu Y, Cai Y, Li Z, Ye F Front Pharmacol. 2022; 13:1053610.

PMID: 36408246 PMC: 9672319. DOI: 10.3389/fphar.2022.1053610.


The Glycosyltransferase Pathway: An Integrated Analysis of the Cell Metabolome.

Audet-Delage Y, Rouleau M, Villeneuve L, Guillemette C Metabolites. 2022; 12(10).

PMID: 36295907 PMC: 9609030. DOI: 10.3390/metabo12101006.