Mechanism of cytotoxicity of 5,10-dideazatetrahydrofolic acid in human ovarian carcinoma cells in vitro and modulation of the drug activity by folic or folinic acid folic or folinic acid

E. Erba, S. Sent, C. Sessa, F. L. Vikhanskayat, M. D'Incalcit

Research output: Contribution to journalArticle

Abstract

Inhibition of clonogenic potential by the glycinamideribonucleosyl transformylase inhibitor 5,10dideazatetrahydrofolic acid (DDATHF, Lometrexol) was evaluated in vitro in a human ovarian carcinoma cell line, SW626. Drug-induced inhibition of clonogenic potential is a function of the dose and time of exposure and is independent of the formation of DNA single-strand breaks or de novo synthesis of protein. Simultaneous treatment with 100 μM hypoxanthine completely prevented the inhibition of clonogenic potential caused by 0.5 μM DDATHF. DDATHF blocked cells in the early-middle S-phases of the cell cycle, and there was a correponding marked reduction in the rate of DNA synthesis after drug withdrawal. The cytotoxic potential of DDATHF was modulated by the folic acid concentration present in the medium. In a medium containing 0.22 μM folic acid, DDATHF cytotoxicity was at least 100 times that in a regular medium containing 2.22 μM folic acid, levels which, however, are about 100 times those found in human plasma. DDATHF cytotoxicity differed moderately when folic acid concentrations varied between 0.22 and 0 μM, suggesting that folic acid does not necessarily antagonise DDATHF anti-tumour activity. Folinic acid at a concentration as low as 0.1 μM can completely rescue cells when given simultaneously with 0.5 μM DDATHF. When folinic acid was given 24 h after DDATHF, a reversal of cytotoxicity was observed at 0.5 and 1 μM but to a much lesser extent than simultaneous treatment. When folinic acid was added after 48 or 72 h of DDATHF washout, even at a high concentration and for a long time, no reduction in DDATHF cytotoxicity was found. In conclusion, the study highlights the modulation of DDATHF cytotoxicity by folic acid or by folinic acid and provides further rationale for in vivo clinical investigation with these combinations.

Original languageEnglish
Pages (from-to)205-211
Number of pages7
JournalBritish Journal of Cancer
Volume69
Issue number2
Publication statusPublished - Feb 1994

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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