Expression and Functional Characterization of Breast Cancer-Associated Cytochrome P450 4Z1 in Saccharomyces cerevisiae

Drug Metab Dispos. 2017 Dec;45(12):1364-1371. doi: 10.1124/dmd.117.078188. Epub 2017 Oct 10.

Abstract

CYP4Z1 is an "orphan" cytochrome P450 (P450) enzyme that has provoked interest because of its hypothesized role in breast cancer through formation of the signaling molecule 20-hydroxyeicosatetraenoic acid (20-HETE). We expressed human CYP4Z1 in Saccharomyces cerevisiae and evaluated its catalytic capabilities toward arachidonic and lauric acids (AA and LA). Specific and sensitive mass spectrometry assays enabled discrimination of the regioselectivity of hydroxylation of these two fatty acids. CYP4Z1 generated 7-, 8-, 9-, 10-, and 11-hydroxy LA, whereas the 12-hydroxy metabolite was not detected. HET0016, the prototypic CYP4 inhibitor, only weakly inhibited laurate metabolite formation (IC50 ∼15 μM). CYP4Z1 preferentially oxidized AA to the 14(S),15(R)-epoxide with high regioselectivity and stereoselectivity, a reaction that was also insensitive to HET0016, but neither 20-HETE nor 20-carboxy-AA were detectable metabolites. Docking of LA and AA into a CYP4Z1 homology model was consistent with this preference for internal fatty acid oxidation. Thus, human CYP4Z1 has an inhibitor profile and product regioselectivity distinct from most other CYP4 enzymes, consistent with CYP4Z1's lack of a covalently linked heme. These data suggest that, if CYP4Z1 modulates breast cancer progression, it does so by a mechanism other than direct production of 20-HETE.

MeSH terms

  • Amidines / pharmacology
  • Breast Neoplasms / metabolism*
  • Cytochrome P450 Family 4 / antagonists & inhibitors
  • Cytochrome P450 Family 4 / chemistry
  • Cytochrome P450 Family 4 / isolation & purification
  • Cytochrome P450 Family 4 / metabolism*
  • Disease Progression
  • Humans
  • Hydroxyeicosatetraenoic Acids / metabolism*
  • Hydroxylation / drug effects
  • Interleukin-1 Receptor-Associated Kinases
  • Lauric Acids / metabolism*
  • Mass Spectrometry
  • Microsomes, Liver
  • Molecular Docking Simulation
  • Oxidation-Reduction / drug effects
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae

Substances

  • Amidines
  • HET0016
  • Hydroxyeicosatetraenoic Acids
  • Lauric Acids
  • Recombinant Proteins
  • 20-hydroxy-5,8,11,14-eicosatetraenoic acid
  • CYP4Z1 protein, human
  • Cytochrome P450 Family 4
  • Interleukin-1 Receptor-Associated Kinases