Human gene families encoding UDP-Glucuronosyltransferases (UGTs) have been
identified and partially characterised. This family of enzymes catalysed th
e glucuronidation of drugs, xenobiotics and endobiotics. Genetic mutations
and polymorphisms have been identified in several UGT genes and examples sh
ould be anticipated in all UGT genes. A common genetic defect in the TATA b
ox promoter of the UGT1A1 gene is associated with Gilbert's Syndrome (GS) c
ausing mild hyperbilirubinaemia. Recently, adverse effects of anticancer ag
ents have been observed in Gilbert's patients due to reduced drug or biliru
bin glucuronidation. (C) 2000 Elsevier Science Ireland Ltd. All rights rese
rved.