Cytosolic and microsomal activation of doxifluridine and tegafur to produce 5-fluorouracil in human liver

Cancer Chemother Pharmacol. 2002 Dec;50(6):454-8. doi: 10.1007/s00280-002-0528-1. Epub 2002 Oct 26.

Abstract

Purpose: The enzymatic formation of 5-fluorouracil (5-FU) from two fluoropyrimidine prodrugs, doxifluridine (5'-DFUR) and tegafur (FT), was compared in vitro in order to determine whether there are differences between the metabolic profiles of the two prodrugs.

Methods: Conversion of the two fluoropyrimidine prodrugs to 5-FU was measured by high-performance liquid chromatography at a concentration of 500 micro M using the microsomal and cytosolic fractions of 12 human livers. The degree of correlation between the 5-FU-forming activities was determined using various cytochrome P450-dependent reactions.

Results: Liver microsomes catalyzed 5-FU formation from 5'-DFUR at rates of 10.0-160.1 pmol/min per mg protein and correlated well with CYP2A6-dependent coumarin 7-hydroxylase activity. The rates of microsomal 5-FU formation from FT ranged from 44.9 to 808.3 pmol/min per mg protein and also correlated with coumarin 7-hydroxylase activity. The cytosol fractions catalyzed 5-FU formation from 5'-DFUR at rates of 3,164.6 to 6,026.6 pmol/min per mg protein, almost two orders of magnitude higher than the rates of cytosolic 5-FU formation from FT (46.8-219.0 pmol/min per mg protein).

Conclusions: The cytosolic enzymes in livers appear to be important for 5-FU formation from 5'-DFUR. Both cytosolic and microsomal enzymes were involved almost equally in 5-FU formation from FT. The increased formation of 5-FU from 5'-DFUR might provide an answer to the question of why similar blood 5-FU levels were retained despite blood 5'-DFUR levels lower than blood FT levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Antimetabolites, Antineoplastic / metabolism*
  • Aryl Hydrocarbon Hydroxylases / metabolism
  • Cytochrome P-450 CYP1A2 / metabolism
  • Cytochrome P-450 CYP2A6
  • Cytochrome P-450 Enzyme System / metabolism
  • Cytosol / metabolism*
  • Floxuridine / metabolism*
  • Fluorouracil / metabolism*
  • Humans
  • In Vitro Techniques
  • Microsomes, Liver / enzymology*
  • Mixed Function Oxygenases / metabolism
  • Steroid Hydroxylases / metabolism
  • Tegafur / metabolism*
  • Thymidine Phosphorylase / metabolism

Substances

  • Antimetabolites, Antineoplastic
  • Floxuridine
  • Tegafur
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Steroid Hydroxylases
  • Aryl Hydrocarbon Hydroxylases
  • CYP2A6 protein, human
  • Cytochrome P-450 CYP1A2
  • Cytochrome P-450 CYP2A6
  • steroid hormone 6-beta-hydroxylase
  • Thymidine Phosphorylase
  • Fluorouracil
  • doxifluridine