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A comparative study on proliferation, macromolecular synthesis and energy metabolism of in vitro-grown Ehrlich ascites tumor cells in the presence of glucosone, galactosone and methylglyoxal.

Abstract
Proliferation of in vitro grown Ehrlich ascites tumor cells is completely inhibited by 0.2-0.4 mM methylglyoxal and 1-2 mM glucosone or galactosone without severely affecting viability (dye exclusion test); no phase-specific arrest of cell growth is observed. Incorporation of [14C] thymidine into the acid-insoluble fraction of the cells decreases within a few minutes to less than 50% of that in controls in the presence of 0.4 mM methylglyoxal, and 2 mM glucosone or galactosone causes a comparable inhibition of DNA synthesis after 2 h or 4 h, respectively. The action of 0.4 mM methylglyoxal inhibits incorporation of [14C] leucine within a few minutes by more than 70%, while 2 mM glucosone and galactosone are significantly less effective (50%-60% inhibition after 12 h). While methylglyoxal and galactosone do not severely affect lactate production of the cells, 2 mM glucosone reduces glycolysis by 60%-70%; ATP/ADP ratios did not fall below 3.5 in the presence of the inhibitors (controls 4-6). It is suggested that the reaction potentialities of the oxaldehyde function of the inhibitors play an important role in their growth-inhibitory activity, besides exerting a specific effect on hexokinase (glucosone) and UTP-trapping activity.
AuthorsK A Reiffen, F Schneider
JournalJournal of cancer research and clinical oncology (J Cancer Res Clin Oncol) Vol. 107 Issue 3 Pg. 206-10 ( 1984) ISSN: 0171-5216 [Print] Germany
PMID6736108 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Aldehydes
  • DNA, Neoplasm
  • Ketoses
  • Neoplasm Proteins
  • glucosone
  • galactosone
  • Adenosine Diphosphate
  • Pyruvaldehyde
  • Adenosine Triphosphate
  • Galactose
Topics
  • Adenosine Diphosphate (metabolism)
  • Adenosine Triphosphate (metabolism)
  • Aldehydes (pharmacology)
  • Animals
  • Carcinoma, Ehrlich Tumor (metabolism, pathology)
  • Cell Division (drug effects)
  • Cell Survival (drug effects)
  • DNA, Neoplasm (biosynthesis)
  • Energy Metabolism (drug effects)
  • Female
  • Galactose (analogs & derivatives, pharmacology)
  • Ketoses (pharmacology)
  • Mice
  • Mice, Inbred Strains
  • Neoplasm Proteins (biosynthesis)
  • Pyruvaldehyde (pharmacology)

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