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Ability of sera from mice treated with Ge-132, an organic germanium compound, to inhibit experimental murine ascites tumours.

Abstract
Sera from C57Bl/6 mice treated orally with Ge-132 exhibited antitumour activity against Ehrlich (allogeneic) and RL male 1 (syngeneic) ascites tumours in BALB/c mice. Sera obtained from mice 24 h after Ge-132 administration displayed the greatest antitumour effect and this was dose dependent. Sera prepared from mice 12, 36, or 48 h after Ge-132 treatment had no protective effect. Circulating interferon (IFN) was induced at 24 h after administration of Ge-132 but was not detected in the sera at 12, 36, or 48 h after administration. The antiviral activity of sera from Ge-132-treated mice was inactivated by treatments with trypsin, low pH, and anti-IFN gamma antiserum. The inactivated preparations of serum IFN induced by Ge-132 did not exhibit antitumour activity when administered to tumour-bearing mice. These results suggest that antitumour activity in the sera of Ge-132-treated mice may be expressed through activities of Ge-132-induced lymphokine(s), such as IFN gamma.
AuthorsF Suzuki, R R Brutkiewicz, R B Pollard
JournalBritish journal of cancer (Br J Cancer) Vol. 52 Issue 5 Pg. 757-63 (Nov 1985) ISSN: 0007-0920 [Print] England
PMID3933536 (Publication Type: Journal Article)
Chemical References
  • Organometallic Compounds
  • Propionates
  • Germanium
  • propagermanium
  • Interferon-gamma
Topics
  • Animals
  • Carcinoma, Ehrlich Tumor (therapy)
  • Dose-Response Relationship, Immunologic
  • Female
  • Germanium (pharmacology)
  • Interferon-gamma (antagonists & inhibitors, blood)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Neoplasms, Experimental (mortality, therapy)
  • Organometallic Compounds (pharmacology)
  • Propionates
  • Time Factors

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