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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1983-5-27
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pubmed:abstractText |
The effects of tumor promoters on the expression of murine leukemia virus (MuLV) were studied in tissue culture. Dihydroteleocidin B, an indole alkaloid, recently found to be a tumor promoter, enhanced not only the production of Moloney MuLV (M-MuLV) by a mouse fibroblast cell line, C3H2K, persistently infected with M-MuLV, but also growth on the C3H2K cells. The production of infectious M-MuLV by M-MuLV-infected C3H2K cells that had been treated with dihydroteleocidin B for 1-7 days was four or five times higher than that of control cells. C3H2K cells grew faster and became stationary at higher cell densities in the presence of dihydroteleocidin B than in its absence. The tumor-promoting phorbol ester phorbol-12, 13-didecanoate and 12-O-tetradecanoylphorbol-13-acetate also enhanced the production of M-MuLV, but their effects were not so strong as that of dihydroteleocidin B. These tumor promoters, however, did not induce production of endogenous MuLV in C3H2K or K-BALB cells.
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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 |
Apr
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
509-13
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pubmed:dateRevised |
2007-7-24
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pubmed:meshHeading |
pubmed-meshheading:6832857-Alkaloids,
pubmed-meshheading:6832857-Animals,
pubmed-meshheading:6832857-Carcinogens,
pubmed-meshheading:6832857-Cell Division,
pubmed-meshheading:6832857-Cell Line,
pubmed-meshheading:6832857-Fibroblasts,
pubmed-meshheading:6832857-Lyngbya Toxins,
pubmed-meshheading:6832857-Mice,
pubmed-meshheading:6832857-Moloney murine leukemia virus,
pubmed-meshheading:6832857-Time Factors,
pubmed-meshheading:6832857-Virus Replication
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pubmed:year |
1983
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pubmed:articleTitle |
A new tumor promoter, dihydroteleocidin B, enhances cell growth and the production of murine leukemia virus by fibroblasts.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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