Abstract
The antiandrogenic drug, flutamide, is widely used in the treatment of carcinoma of the prostate. The present study examines the metabolism of flutamide by human liver microsomes and purified recombinant human cytochrome P450s (CYP), expressed as fusion proteins. These studies show the principal role of CYP1A2 in the metabolism of flutamide to 2-hydroxyflutamide. A minor metabolite is formed during the metabolism of flutamide by CYP3A4 in the presence of an excess of added purified NADPH-P450 reductase.
The metabolism of flutamide is inhibited by low concentrations of α-naphthoflavone and ketoconazole. Other substrates of CYP1A2, such as phenacetin, imipramine, caffeine, and estradiol, are also inhibitors of flutamide metabolism by CYP1A2. Of interest is the inhibition of flutamide metabolism by its metabolite, 2-hydroxyflutamide, and the inhibition of the 2- and 4- hydroxylation of estradiol by flutamide.
CV1 cells do not metabolize flutamide to 2-hydroxyflutamide. In assays performed using this cell line transfected with the cDNA for the androgen receptor, flutamide is a pure antagonist, and 2-hydroxyflutamide, while a more potent androgen receptor (AR) antagonist, activates the AR at higher concentrations. Stable expression of CYPIA2 in these CV1 cells causes flutamide to exhibit agonistic properties at higher concentrations, a behavior not exhibited by cells stably transfected only with the expression vector encoding the AR. These findings raise the possibility that increased conversion of flutamide to 2-hydroxyflutamide or accumulation of 2-hydroxyflutamide in cells may contribute to the anomalous responses to flutamide that are observed in some advanced prostate cancers.
Footnotes
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Send reprint requests to: Ronald W. Estabrook, Ph.D., Department of Biochemistry, University of Texas, Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75235-9038. E-mail:estabroo{at}utsw.swmed.edu.
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This study was supported by National Institutes of Health Grants NIGMS 16488-27 (to R.W.E.) and DK 47657 (to M.J.M.) and by Grant I-1090 from the Robert A Welch Foundation (to M.J.M.). The tritiation of samples of flutamide and hydroxyflutamide were underwritten by an unrestricted educational grant from Integrated Therapeutics Group.
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↵2 T. S. Gao and M. J. McPhaul: Functional activities of the A- and B-forms of the human androgen receptor in response to androgen receptor agonists and antagonists, submitted for publication.
- Abbreviations used are::
- CYP
- cytochrome P450
- DOPC
- dioleoylphospatidyl-choline
- CHAPS
- (3-[3-cholamidopropyl)-dimethylammonio]1-propanesulfonate
- AR
- androgen receptor
- HPLC
- high performance liquid chromatography
- CMV
- cytomegalovirus
- Received April 25, 1997.
- Accepted July 9, 1997.
- The American Society for Pharmacology and Experimental Therapeutics
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