Selective metabolism of vincristine in vitro by CYP3A5

Jennifer B. Dennison, Palaniappan Kulanthaivel, Robert J. Barbuch, Jamie Renbarger, William J. Ehlhardt, Stephen D. Hall

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

Clinical outcomes of vincristine therapy, both neurotoxicity and efficacy, are unpredictable, and the reported pharmacokinetics of vincristine have considerable interindividual variability. In vitro and in vivo data support a dominant role for CYP3A enzymes in the elimination of vincristine. Consequently, genetic polymorphisms in cytochrome P450 (P450) expression may contribute to the interindividual variability in clinical response, but the contributions of individual P450s and the primary pathways of vincristine metabolism have not been defined. In the present study, vincristine was incubated with a library of cDNA-expressed P450s, and the major oxidative metabolites were identified. CYP3A4 and CYP3A5 were the only P450s to support substantial loss of parent drug and formation of the previously unidentified, major metabolite (M1). The structure of M1, arising as a result of an oxidative cleavage of the piperidine ring of the dihydro-hydroxycatharanthine unit of vincristine, was conclusively established after conversion to suitable derivatives followed by spectroscopic analysis, and a new pathway for vincristine metabolism is proposed. CYP3A5 was more efficient in catalyzing the formation of M1 compared with CYP3A4 (9- to 14-fold higher intrinsic clearance for CYP3A5). The formation of M1 was stimulated (3-fold) by the presence of coexpressed cytochrome b5, but the relative efficiencies of M1 formation by CYP3A4 and CYP3A5 were unaffected. Our findings demonstrate that in contrast to most CYP3A biotransformations, the oxidation of vincristine is considerably more efficient with CYP3A5 than with CYP3A4. We conclude that common genetic polymorphisms in CYP3A5 expression may contribute to the interindividual variability in the systemic elimination of vincristine.

Original languageEnglish
Pages (from-to)1317-1327
Number of pages11
JournalDrug Metabolism and Disposition
Volume34
Issue number8
DOIs
StatePublished - 2006

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Cytochrome P-450 CYP3A
Vincristine
Metabolism
Genetic Polymorphisms
Metabolites
Polymorphism
In Vitro Techniques
Cytochromes b5
Pharmacokinetics
Spectroscopic analysis
Biotransformation
Gene Library
Cytochrome P-450 Enzyme System

ASJC Scopus subject areas

  • Pharmacology
  • Toxicology

Cite this

Dennison, J. B., Kulanthaivel, P., Barbuch, R. J., Renbarger, J., Ehlhardt, W. J., & Hall, S. D. (2006). Selective metabolism of vincristine in vitro by CYP3A5. Drug Metabolism and Disposition, 34(8), 1317-1327. https://doi.org/10.1124/dmd.106.009902

Selective metabolism of vincristine in vitro by CYP3A5. / Dennison, Jennifer B.; Kulanthaivel, Palaniappan; Barbuch, Robert J.; Renbarger, Jamie; Ehlhardt, William J.; Hall, Stephen D.

In: Drug Metabolism and Disposition, Vol. 34, No. 8, 2006, p. 1317-1327.

Research output: Contribution to journalArticle

Dennison, JB, Kulanthaivel, P, Barbuch, RJ, Renbarger, J, Ehlhardt, WJ & Hall, SD 2006, 'Selective metabolism of vincristine in vitro by CYP3A5', Drug Metabolism and Disposition, vol. 34, no. 8, pp. 1317-1327. https://doi.org/10.1124/dmd.106.009902
Dennison, Jennifer B. ; Kulanthaivel, Palaniappan ; Barbuch, Robert J. ; Renbarger, Jamie ; Ehlhardt, William J. ; Hall, Stephen D. / Selective metabolism of vincristine in vitro by CYP3A5. In: Drug Metabolism and Disposition. 2006 ; Vol. 34, No. 8. pp. 1317-1327.
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