Transfer of intestine-derived diamines into tumour cells during treatment of Ehrlich-ascites--carcinoma-bearing mice with polyamine anti-metabolites

Biochem J. 1984 Mar 1;218(2):641-4. doi: 10.1042/bj2180641.

Abstract

Treatment of Ehrlich-ascites-carcinoma-bearing mice with methylglyoxal bis(guanylhydrazone) alone or in combination with 2-difluoromethylornithine greatly enhanced the transfer of intragastrically administered radioactive putrescine and cadaverine into the carcinoma cells. Difluoromethylornithine alone did not have any effect on the accumulation of intestine-derived diamines in the tumour cells. The frequently reported restoration of difluoromethylornithine-induced polyamine depletion on administration of methylglyoxal bis(guanylhydrazone) is in all likelihood attributable to a profound inhibition of intestinal diamine oxidase (EC 1.4.3.6), resulting in an enhanced entry of intestinal (bacterial) diamines into general circulation and finally into tumour cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cadaverine / metabolism*
  • Carcinoma, Ehrlich Tumor / metabolism*
  • Diamines / metabolism*
  • Eflornithine
  • Guanidines / pharmacology*
  • Mice
  • Mitoguazone / pharmacology*
  • Ornithine / analogs & derivatives*
  • Ornithine / pharmacology
  • Putrescine / metabolism*

Substances

  • Diamines
  • Guanidines
  • Ornithine
  • Cadaverine
  • Mitoguazone
  • Putrescine
  • Eflornithine