Abstract |
(-)- Emetine has little or no effect on O(2) consumption of Ehrlich ascites-cell suspensions or on the viability of transplanted Ehrlich ascites-tumour cells exposed to, or incubated with, the drug in vitro before inoculation into new-host mice. (-)- Emetine administered as a single injection to mice bearing Ehrlich ascites-tumour cells slows the growth rate of the tumour. The subcutaneous or intraperitoneal injection of the drug depresses protein and DNA synthesis of the tumour cells in vivo in a reversible manner. Mice bearing ascitic sarcoma 180 or Ehrlich ascites-tumour cells when given a course of treatment with (-)- emetine or (-)- O-methyltubulosine have a substantially lower tumour load than untreated controls and correspondingly longer survival times.
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Authors | R K Johnson, W R Jondorf |
Journal | The Biochemical journal
(Biochem J)
Vol. 140
Issue 1
Pg. 87-94
(Apr 1974)
ISSN: 0264-6021 [Print] England |
PMID | 4451553
(Publication Type: Journal Article)
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Chemical References |
- DNA, Neoplasm
- Neoplasm Proteins
- O-methyltubulosine
- Leucine
- Thymidine
- Emetine
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Topics |
- Animals
- Carcinoma, Ehrlich Tumor
(metabolism)
- DNA, Neoplasm
(biosynthesis)
- Emetine
(analogs & derivatives, pharmacology)
- Leucine
(metabolism)
- Mice
- Mice, Inbred ICR
- Neoplasm Proteins
(biosynthesis)
- Neoplasm Transplantation
- Oxygen Consumption
(drug effects)
- Protein Biosynthesis
(drug effects)
- Sarcoma 180
(metabolism)
- Thymidine
(metabolism)
- Time Factors
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