Publication detail

Identification of enzymes oxidizing the tyrosine kinase inhibitor cabozantinib: Cabozantinib is predominantly oxidized by CYP3A4 and its oxidation is stimulated by cyt b5 activity

INDRA, R. VAVROVÁ, K. POMPACH, P. HEGER, Z. HODEK, P.

Original Title

Identification of enzymes oxidizing the tyrosine kinase inhibitor cabozantinib: Cabozantinib is predominantly oxidized by CYP3A4 and its oxidation is stimulated by cyt b5 activity

Type

journal article in Web of Science

Language

English

Original Abstract

Herein, the in vitro metabolism of tyrosine kinase inhibitor cabozantinib, the drug used for the treatment of metastatic medullary thyroid cancer and advanced renal cell carcinoma, was studied using hepatic microsomal samples of different human donors, human recombinant cytochromes P450 (CYPs), flavin-containing mono-oxygenases (FMOs) and aldehyde oxidase. After incubation with human microsomes, three metabolites, namely cabozantinib N-oxide, desmethyl cabozantinib and monohydroxy cabozantinib, were detected. Significant correlations were found between CYP3A4 activity and generation of all metabolites. The privileged role of CYP3A4 was further confirmed by examining the effect of CYP inhibitors and by human recombinant enzymes. Only four of all tested human recombinant cytochrome P450 were able to oxidize cabozantinib, and CYP3A4 exhibited the most efficient activity. Importantly, cytochrome b(5) (cyt b(5)) stimulates the CYP3A4-catalyzed formation of cabozantinib metabolites. In addition, cyt b(5) also stimulates the activity of CYP3A5, whereas two other enzymes, CYP1A1 and 1B1, were not affected by cyt b(5). Since CYP3A4 exhibits high expression in the human liver and was found to be the most efficient enzyme in cabozantinib oxidation, we examined the kinetics of this oxidation. The present study provides substantial insights into the metabolism of cabozantinib and brings novel findings related to cabozantinib pharmacokinetics towards possible utilization in personalized medicine.

Keywords

cabozantinib; cytochrome P450; tyrosine kinase inhibitor; cytochrome b(5)

Authors

INDRA, R.; VAVROVÁ, K.; POMPACH, P.; HEGER, Z.; HODEK, P.

Released

30. 12. 2020

Publisher

MDPI

ISBN

2227-9059

Periodical

Biomedicines

Year of study

8

Number

12

State

Swiss Confederation

Pages from

1

Pages to

14

Pages count

14

URL

Full text in the Digital Library

BibTex

@article{BUT169451,
  author="Radek {Indra} and Katarína {Vavrová} and Petr {Pompach} and Zbyněk {Heger} and Petr {Hodek}",
  title="Identification of enzymes oxidizing the tyrosine kinase inhibitor cabozantinib: Cabozantinib is predominantly oxidized by CYP3A4 and its oxidation is stimulated by cyt b5 activity",
  journal="Biomedicines",
  year="2020",
  volume="8",
  number="12",
  pages="1--14",
  doi="10.3390/biomedicines8120547",
  issn="2227-9059",
  url="https://www.mdpi.com/2227-9059/8/12/547"
}