pubmed-article:2965156 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C1261473 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0024109 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0017968 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0431085 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0041385 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0085535 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C1522484 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0036525 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0392747 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C1554963 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0049517 | lld:lifeskim |
pubmed-article:2965156 | lifeskim:mentions | umls-concept:C0673362 | lld:lifeskim |
pubmed-article:2965156 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:2965156 | pubmed:dateCreated | 1988-5-6 | lld:pubmed |
pubmed-article:2965156 | pubmed:abstractText | Synthesis and expression of cell surface carbohydrates appear to be involved in recognition events associated with tumor invasion and metastasis. Thus, the potential of murine sarcoma L-1 cells to form experimental lung metastases after i.v. injection was assessed after inhibiting tumor cell protein glycosylation with tunicamycin, swainsonine, bromoconduritol, or 1-desoxynojirimycin. Incubation of sarcoma L-1 cells with 0.5 microgram (or above) of these substances/ml medium for 20-24 h significantly inhibited lung colonization. Cytotoxic side effects or additional organ manifestations could not be found. Gas liquid chromatographic examinations of carbohydrates from treated L-1 cells indicated that sugar synthesis was evidently inhibited. These results suggest that specific glycan structures on tumor cells are required for expression of the metastatic phenotype. | lld:pubmed |
pubmed-article:2965156 | pubmed:language | eng | lld:pubmed |
pubmed-article:2965156 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2965156 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2965156 | pubmed:issn | 0171-5216 | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:UhlenbruckGG | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:PulvererGG | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:KoH LHL | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:OhshimaYY | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:YassinAA | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:RoszkowskiKK | lld:pubmed |
pubmed-article:2965156 | pubmed:author | pubmed-author:BeuthJJ | lld:pubmed |
pubmed-article:2965156 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2965156 | pubmed:volume | 114 | lld:pubmed |
pubmed-article:2965156 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2965156 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2965156 | pubmed:pagination | 217-20 | lld:pubmed |
pubmed-article:2965156 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:2965156 | pubmed:meshHeading | pubmed-meshheading:2965156-... | lld:pubmed |
pubmed-article:2965156 | pubmed:year | 1988 | lld:pubmed |
pubmed-article:2965156 | pubmed:articleTitle | Glycoprotein modifications of sarcoma L-1 tumor cells by tunicamycin, swainsonine, bromoconduritol or 1-desoxynojirimycin treatment inhibits their metastatic lung colonization in Balb/c-mice. | lld:pubmed |
pubmed-article:2965156 | pubmed:affiliation | Institute of Hygiene, University of Cologne, Federal Republic of Germany. | lld:pubmed |
pubmed-article:2965156 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2965156 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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