Abstract |
An artificial hematogenous- metastasis model, in which B16f10 melanoma cells injected into the tail veins of C57/BL mice arrest in the lungs and proliferate as discrete pulmonary foci, was employed to examine effects of L- histidinol on the capacity of a number of conventional antineoplastic agents to manage disseminated disease. Treatment responses were evaluated by determining both the number of lung foci and/or by evaluating animal survival. L- Histidinol, on its own, was found to have a significant and dose-dependent capacity to reduce the number of lung foci and to extend survival of animals bearing disseminated B16f10 melanoma. L- Histidinol enhanced the ability of bis-chloroethylnitrosourea, 5-fluorouracil, and 1-beta-D-arabinofuranosulcytosine to reduce the number of lung foci. The latter combinations also gave marked improvements in survival, whether administered 1 or 7 days after the intravenous injection of tumor cells.
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Authors | R C Warrington, W D Fang |
Journal | Anticancer research
(Anticancer Res)
1991 Sep-Oct
Vol. 11
Issue 5
Pg. 1869-74
ISSN: 0250-7005 [Print] Greece |
PMID | 1722659
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cytarabine
- Bleomycin
- Histidine
- Histidinol
- Doxorubicin
- Cisplatin
- Fluorouracil
- Carmustine
- Methotrexate
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Topics |
- Animals
- Antineoplastic Combined Chemotherapy Protocols
(therapeutic use)
- Bleomycin
(administration & dosage)
- Carmustine
(administration & dosage)
- Cisplatin
(administration & dosage)
- Cytarabine
(administration & dosage)
- Doxorubicin
(administration & dosage)
- Drug Interactions
- Drug Screening Assays, Antitumor
- Female
- Fluorouracil
(administration & dosage)
- Histidine
(pharmacology)
- Histidinol
(administration & dosage, antagonists & inhibitors)
- Lung Neoplasms
(drug therapy, mortality, secondary)
- Melanoma, Experimental
(drug therapy, mortality, secondary)
- Methotrexate
(administration & dosage)
- Mice
- Mice, Inbred C57BL
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