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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1994-9-19
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pubmed:abstractText |
The antitumor efficacy of recombinant murine interleukin-1 alpha (rMuIL-1 alpha) was evaluated either alone or in combination with recombinant human hybrid interferon alpha A/D (IFN-alpha A/D) against the murine B16 F10 malignant melanoma. Treatment of subcutaneous tumor-bearing mice intraperitoneally with rMuIL-1 alpha resulted in a dose-dependent inhibition of tumor growth with the greatest activity obtained with the maximum tolerated dose of rMuIL-1 alpha (10 micrograms per treatment). Augmented tumor inhibition comparable to that seen in mice treated with a high dose of rMuIL-1 alpha was observed in subcutaneous tumor-bearing mice injected with the combination of IFN-alpha A/D and a low dose of rMuIL-1 alpha. Similar inhibition of subcutaneous tumor growth was obtained in T-cell-deficient nude or natural killer cell-deficient beige mice. In contrast, treatment of mice bearing B16F10 experimental pulmonary metastases with rMuIL-1 alpha resulted in no decrease in the number of metastases, and rMuIL-1 alpha did not potentiate the antimetastatic activity of IFN-alpha A/D. A synergistic induction of IL-6 was induced in mice treated with the combination of rMuIL-1 alpha plus IFN-alpha A/D but the level of IL-6 induced was not correlated with inhibition of tumor growth because this elevation of IL-6 was not observed in tumor-bearing nude mice. No direct antiproliferative activity was demonstrable in vitro against B16 F10 cells with rMuIL-1 alpha, IL-6, or rMuIL-1 alpha plus IL-6, and addition of these cytokines did not enhance the antiproliferative activity of IFN-alpha A/D.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1067-5582
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
233-41
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:8061895-Animals,
pubmed-meshheading:8061895-Female,
pubmed-meshheading:8061895-Interferon-alpha,
pubmed-meshheading:8061895-Interleukin-1,
pubmed-meshheading:8061895-Interleukin-6,
pubmed-meshheading:8061895-Killer Cells, Natural,
pubmed-meshheading:8061895-Lung Neoplasms,
pubmed-meshheading:8061895-Lymphocyte Activation,
pubmed-meshheading:8061895-Melanoma, Experimental,
pubmed-meshheading:8061895-Mice,
pubmed-meshheading:8061895-Mice, Inbred C57BL,
pubmed-meshheading:8061895-Mice, Mutant Strains,
pubmed-meshheading:8061895-Mice, Nude,
pubmed-meshheading:8061895-Recombinant Proteins,
pubmed-meshheading:8061895-Skin Neoplasms,
pubmed-meshheading:8061895-T-Lymphocytes,
pubmed-meshheading:8061895-Tumor Cells, Cultured
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pubmed:year |
1994
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pubmed:articleTitle |
Enhanced antitumor efficacy in mice by combination treatment with interleukin-1 alpha and interferon-alpha.
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pubmed:affiliation |
Department of Oncology, Roche Research Center, Hoffmann-La Roche Inc., Nutley, New Jersey 07110.
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pubmed:publicationType |
Journal Article
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