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Hyperthermia enhances the cytotoxicity against hypoxic cells of RP-170, a new 2-nitroimidazole nucleoside hypoxic cell sensitizer.

Abstract
The effect of the new hypoxic cell sensitizer, 1-[2-hydroxy-1-(hydroxymethyl)-ethoxy]methyl-2-nitroimidazole (RP-170), combined with heat against EMT6/KU cells, was determined under conditions of in vitro hypoxia. Heat-induced cytotoxicity for the EMT6/KU cells was increased to a greater extent under conditions of hypoxia and a normal pH of the medium. Hypoxia also reduced the surviving fraction of the cells treated either with RP-170 alone or with RP-170 plus heat. The concomitant treatment of RP-170 and heat inhibited the clonogenic activity of the EMT6/KU cells under conditions of in vitro hypoxia in all experimental groups, with a significant difference (p < 0.05). Therefore, RP-170 combined with exposure to heat may be an effective treatment for hypoxic cells in a solid tumor, as these cells are resistant to radiation and/or to many chemotherapeutic agents.
AuthorsY Emi, Y Maehara, T Kusumoto, H Baba, M Sakaguchi, K Sugimachi
JournalOncology (Oncology) 1995 Jan-Feb Vol. 52 Issue 1 Pg. 55-9 ISSN: 0030-2414 [Print] Switzerland
PMID7800343 (Publication Type: Journal Article)
Chemical References
  • Nitroimidazoles
  • Nucleosides
  • Radiation-Sensitizing Agents
  • RP 170
  • Misonidazole
Topics
  • Animals
  • Cell Hypoxia
  • Cell Survival (drug effects)
  • Female
  • Hot Temperature
  • Mice
  • Mice, Inbred BALB C
  • Misonidazole (pharmacology)
  • Nitroimidazoles (pharmacology)
  • Nucleosides (pharmacology)
  • Radiation-Sensitizing Agents (pharmacology)
  • Tumor Cells, Cultured

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