In vitro assessment of fluoropyrimidine-metabolizing enzymes: Dihydropyrimidine dehydrogenase, dihydropyrimidinase, and β-ureidopropionase

Eiji Hishinuma, Evelyn Gutiérrez Rico, Masahiro Hiratsuka

Research output: Contribution to journalReview articlepeer-review

5 Citations (Scopus)


Fluoropyrimidine drugs (FPs), including 5-fluorouracil, tegafur, capecitabine, and doxifluridine, are among the most widely used anticancer agents in the treatment of solid tumors. However, severe toxicity occurs in approximately 30% of patients following FP administration, emphasizing the importance of predicting the risk of acute toxicity before treatment. Three metabolic enzymes, dihydropyrimidine dehydrogenase (DPD), dihydropyrimidinase (DHP), and β-ureidopropionase (β-UP), degrade FPs; hence, deficiencies in these enzymes, arising from genetic polymorphisms, are involved in severe FP-related toxicity, although the effect of these polymorphisms on in vivo enzymatic activity has not been clarified. Furthermore, the clinical usefulness of current methods for predicting in vivo activity, such as pyrimidine concentrations in blood or urine, is unknown. In vitro tests have been established as advantageous for predicting the in vivo activity of enzyme variants. This is due to several studies that evaluated FP activities after enzyme metabolism using transient expression systems in Escherichia coli or mammalian cells; however, there are no comparative reports of these results. Thus, in this review, we summarized the results of in vitro analyses involving DPD, DHP, and β-UP in an attempt to encourage further comparative studies using these drug types and to aid in the elucidation of their underlying mechanisms.

Original languageEnglish
Article number2342
Pages (from-to)1-21
Number of pages21
JournalJournal of Clinical Medicine
Issue number8
Publication statusPublished - 2020 Aug


  • Dihydropyrimidinase
  • Dihydropyrimidine dehydrogenase
  • Fluoropyrimidine
  • Genetic polymorphism
  • β-ureidopropionase

ASJC Scopus subject areas

  • Medicine(all)


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