Human CYP1B1 and anticancer agent metabolism: mechanism for tumor-specific drug inactivation?

B. Rochat, J. M. Morsman, W. D. Figg, Graeme Ian Murray, H. L. McLeod

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Abstract

The cytochrome P450 1B1 (CYP1B1) is involved in the metabolism of procarcinogens and xenobiotics. Human CYP1B1 protein has been detected in a variety of tumors but is not detected in adjacent normal tissues or in liver. This suggests that CYP1B1 could biotransform anticancer agents specifically in the target cells. The interaction between CYP1B1 and 12 commonly used anticancer drugs was screened using an ethoxyresorufin deethylase assay. Four agents were competitive inhibitors of CYP1B1 activity: flutamide (K-i = 1.0 muM), paclitaxel (K-i = 31.6 muM), mitoxantrone (K-i = 11.6 muM), and docetaxel (K-i = 28.0 muM). Doxorubicin (K-i = 2.6 muM) and daunomycin (K-i = 2.1 muM) were mixed inhibitors, while tamoxifen was a noncompetitive inhibitor (K-i = 5.0 muM). Vinblastine, vincristine, 5-fluorouracil, etoposide, and cyclophosphamide did not inhibit CYP1B1 activity. In vitro incubations with flutamide and CYP1B1 produced a metabolite consistent with 2-hydroxyflutamide. Comparison of kinetic parameters (K-m, K-i, V-max) for flutamide 2-hydroxylation by CYP1B1, CYP1A1, and CYP1A2 indicate that CYP1B1 could play a major role for flutamide biotransformation in tumors. The results obtained indicate that several anticancer agents inhibit CYP1B1 activity. Drug inactivation by CYP1B1 may represent a novel mechanism of resistance, influencing the clinical outcome of chemotherapy.

Original languageEnglish
Pages (from-to)537-541
Number of pages4
JournalJournal of Pharmacology and Experimental Therapeutics
Volume296
Issue number2
Publication statusPublished - 2001

Keywords

  • HUMAN CYTOCHROME-P450 1B1
  • XENOBIOTICS
  • EXPRESSION
  • CANCER

Cite this

Human CYP1B1 and anticancer agent metabolism: mechanism for tumor-specific drug inactivation? / Rochat, B.; Morsman, J. M.; Figg, W. D.; Murray, Graeme Ian; McLeod, H. L.

In: Journal of Pharmacology and Experimental Therapeutics, Vol. 296, No. 2, 2001, p. 537-541.

Research output: Contribution to journalArticle

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