Activation of 5’-Deoxy-5-fluorouridine by Thymidine Phosphorylase in Human Tumors

Akira Kono, Yasuhiro Hara, Setsuro Sugata, Yoshiharu Karube, Yoshikazu Matsushima, Hideo Ishitsuka

Research output: Contribution to journalArticle

168 Citations (Scopus)

Abstract

Activities of pyrimidine nucleoside phosphorylases were assayed in extracts of human tumors, normal tissues of the same organs and tumors of mice Sarcoma-180) and guinea pigs Line-10), with thymidine dThd), uridine Urd), and 5’-deoxy-5-fluorouridine 5’-DFUR) as substrates. The nucleoside cleaving activities were higher in extracts of human tumor tissues than in those of normal tissues of the same organs. In human tissues, phosphorolytic activitiy towards dThd was high, while that towards Urd was low. In animal tumors, Urd was the best substrate. 1-2’-Deoxy-β-D-glucopyranosyl)-thymine GPT), a specific inhibitor of uridine phosphorylase, inhibited the phosphorolysis of Urd and 5’-DFUR in extracts of animal tumors, but not that of dThd and 5’-DFUR in extracts of human tumors. A thymidine phosphorylase preparation was partialy purified from human lung cancer. Kmvalues of the preparation were 2.43X10-4M and 1.69X10-3M for dThd and 5’-DFUR, respectively. We conclude that in human tumors a thymidine phosphorylase activity converts 5’-DFUR to 5-fluorouracil, an activated form.

Original languageEnglish
Pages (from-to)175-178
Number of pages4
JournalChemical and Pharmaceutical Bulletin
Volume31
Issue number1
DOIs
Publication statusPublished - 1983 Jan 1

Keywords

  • 1-2’-deoxy-β-D-glucopyranosyl)-thymine
  • 5-fluorouracil
  • 5’-deoxy-5-fluorouridine
  • human tumor
  • lung cancer
  • thymidine
  • thymidine phosphorylase
  • uridine
  • uridine phosphorylase

ASJC Scopus subject areas

  • Chemistry(all)
  • Drug Discovery

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  • Cite this

    Kono, A., Hara, Y., Sugata, S., Karube, Y., Matsushima, Y., & Ishitsuka, H. (1983). Activation of 5’-Deoxy-5-fluorouridine by Thymidine Phosphorylase in Human Tumors. Chemical and Pharmaceutical Bulletin, 31(1), 175-178. https://doi.org/10.1248/cpb.31.175