UPA Perpustakaan Universitas Jember

Archives of Toxicology

Janina Johänning - Personal Name
Werner Schroth - Personal Name
Hiltrud Brauch - Personal Name
Matthias Schwab - Personal Name
Michel Eichelbaum - Personal Name
Astrid Nörenberg - Personal Name
Ulrich M. Zanger - Personal Name
Maria Thomas - Personal Name
Patrick Kröner - Personal Name
Thomas E. Mürdter - Personal Name

Tamoxifen, a standard therapy for breast cancer, is metabolized to compounds with anti-estrogenic as well as estrogen-like
action at the estrogen receptor. Little is known about the formation of estrogen-like metabolites and their biological impact.
Thus, we characterized the estrogen-like metabolites tamoxifen bisphenol and metabolite E for their metabolic pathway
and their influence on cytochrome P450 activity and ADME gene expression. The formation of tamoxifen bisphenol and
metabolite E was studied in human liver microsomes and Supersomes™. Cellular metabolism and impact on CYP enzymes
was analyzed in upcyte® hepatocytes. The influence of 5 µM of tamoxifen, anti-estrogenic and estrogen-like metabolites on
CYP activity was measured by HPLC MS/MS and on ADME gene expression using RT-PCR analyses. Metabolite E was
formed from tamoxifen by CYP2C19, 3A and 1A2 and from desmethyltamoxifen by CYP2D6, 1A2 and 3A. Tamoxifen
bisphenol was mainly formed from (E)- and (Z)-metabolite E by CYP2B6 and CYP2C19, respectively. Regarding phase II
metabolism, UGT2B7, 1A8 and 1A3 showed highest activity in glucuronidation of tamoxifen bisphenol and metabolite E.
Anti-estrogenic metabolites (Z)-4-hydroxytamoxifen, (Z)-endoxifen and (Z)-norendoxifen inhibited the activity of CYP2C
enzymes while tamoxifen bisphenol consistently induced CYPs similar to rifampicin and phenobarbital. On the transcript
level, highest induction up to 5.6-fold was observed for CYP3A4 by tamoxifen, (Z)-4-hydroxytamoxifen, tamoxifen bisphenol
and (E)-metabolite E. Estrogen-like tamoxifen metabolites are formed in CYP-dependent reactions and are further metabolized by glucuronidation. The induction of CYP activity by tamoxifen bisphenol and the inhibition of CYP2C enzymes by
anti-estrogenic metabolites may lead to drug–drug-interactions.

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Tamoxifen
Metabolism
Estrogen-like metabolites
CYP activity
Gene induction

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Archives of Toxicology

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Archives of Toxicology

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