DECREASED IMMUNOSUPPRESSION ASSOCIATED WITH ANTI-TUMOR ACTIVITY OF 5-DEOXY-5-FLUOROURIDINE COMPARED TO 5-FLUOROURACIL AND 5-FLUOROURIDINE

  • 1 January 1983
    • journal article
    • research article
    • Vol. 43  (6) , 2529-2535
Abstract
5-Fluorouracil (5-FUra), 5-deoxy-5-fluorouridine (5''dFUrd), and 5-fluorouridine were compared for their relative antitumor activity, their capacity to inhibit leukocyte exudation and macrophage (M.vphi.) killing of tumor cells in vivo and in vitro, and their ability to induce leukopenia and monocytopenia. 5''dFUrd was less toxic than 5-FUra and exhibited anti-Ehrlich [murine] ascites activity over a wider range of drug doses. Inflammatory exudates induced by thioglycollate or pyran were inhibited up to 91% by prior 5-FUra injection but were inhibited not more than 62% by 5''dFUrd. Pyran-induced M.vphi. inhibition of Ehrlich ascites proliferation in vivo was diminished up to 5-fold by 5-FUra but was never diminished more than 2-fold by 5''dFUrd, while neither agent suppressed in vitro M.vphi. cytotoxicity of in vivo pyran-activated M.vphi.. At high doses, 5-FUra reduced white blood cell counts 73%, in contrast to the 8% reduction caused buy 5''dFUrd, while at their optimal anti-Ehrlich ascites doses, 5-FUra and 5''dFUrd both lowered white blood cell counts by only 20%. However, 5-FUra caused a severe monocytopenia not seen in animals given injections of comparable doses of 5''dFurd. 5-FUra appeared to inhibit the inflammatory response and antitumor activity by inhibiting the influx of immature M.vphi. into the peritoneal cavity, not by inhibiting the function of mature effector cells.