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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6C
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pubmed:dateCreated |
2004-2-25
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pubmed:abstractText |
In our previous study, we found complexes of the non-coding pMP6 plasmid and cationic liposomes which exerted antitumor activity in the C26 model. We now sought to unravel the underlying protective effector mechanism(s).
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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|
pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:issn |
0250-7005
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4843-51
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14981934-Adenocarcinoma,
pubmed-meshheading:14981934-Animals,
pubmed-meshheading:14981934-Cell Division,
pubmed-meshheading:14981934-Cell Survival,
pubmed-meshheading:14981934-Colonic Neoplasms,
pubmed-meshheading:14981934-Cytokines,
pubmed-meshheading:14981934-Drug Carriers,
pubmed-meshheading:14981934-Female,
pubmed-meshheading:14981934-Liposomes,
pubmed-meshheading:14981934-Mice,
pubmed-meshheading:14981934-Mice, Inbred BALB C,
pubmed-meshheading:14981934-Plasmids,
pubmed-meshheading:14981934-Time Factors,
pubmed-meshheading:14981934-Tumor Cells, Cultured
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|
pubmed:articleTitle |
Intraperitoneal administration of pMP6/liposome complexes inhibits the growth of co-localized colon-26 adenocarcinoma cells by inducing a tumor-specific immune response.
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pubmed:affiliation |
Department of General Surgery, University of Vienna Medical School, Vienna, Austria.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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