Title : Potential role of UGT1A4 promoter SNPs in anastrozole pharmacogenomics.

Pub. Date : 2013 Apr

PMID : 23371966






6 Functional Relationships(s)
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1 Potential role of UGT1A4 promoter SNPs in anastrozole pharmacogenomics. Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens
2 In this study, we examined individual variability in the glucuronidation of anastrozole and its association with UGT1A4 promoter and coding region polymorphisms. Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens
3 Anastrozole glucuronidation was correlated (r = 0.99; P < 0.0001) with lamotrigine glucuronidation (a diagnostic substrate for UGT1A4) and with UGT1A4 mRNA expression levels in human liver microsomes (r = 0.99; P < 0.0001). Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens
4 Anastrozole glucuronidation was correlated (r = 0.99; P < 0.0001) with lamotrigine glucuronidation (a diagnostic substrate for UGT1A4) and with UGT1A4 mRNA expression levels in human liver microsomes (r = 0.99; P < 0.0001). Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens
5 Recombinant UGT1A4 catalyzed anastrozole glucuronidation, which was inhibited by hecogenin (IC50 = 15 microM), a UGT1A4 specific inhibitor. Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens
6 Recombinant UGT1A4 catalyzed anastrozole glucuronidation, which was inhibited by hecogenin (IC50 = 15 microM), a UGT1A4 specific inhibitor. Anastrozole UDP glucuronosyltransferase family 1 member A4 Homo sapiens