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.
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Authors | F Suzuki, R R Brutkiewicz, R B Pollard |
Journal | British journal of cancer
(Br J Cancer)
Vol. 52
Issue 5
Pg. 757-63
(Nov 1985)
ISSN: 0007-0920 [Print] England |
PMID | 3933536
(Publication Type: Journal Article)
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Chemical References |
- Organometallic Compounds
- Propionates
- Germanium
- propagermanium
- Interferon-gamma
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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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