Source:http://linkedlifedata.com/resource/pubmed/id/11895479
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2002-3-15
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pubmed:abstractText |
Antimicrotubule drugs (AMDs), such as taxol and vincristine, are the most important addition to the chemotherapeutic armamentarium against human cancers. It has been shown that prolonged AMD treatment induces hyperploidy in G1-checkpoint-defective cancer cells and that these hyperploid cells subsequently undergo apoptosis. However, a fraction of these hyperploid cells are able to survive the prolonged mitotic stress and resume cell-cycle progression.
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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 |
Feb
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pubmed:issn |
1356-9597
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
151-62
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11895479-Antineoplastic Agents,
pubmed-meshheading:11895479-Chromosomes,
pubmed-meshheading:11895479-Glioma,
pubmed-meshheading:11895479-Humans,
pubmed-meshheading:11895479-Microtubules,
pubmed-meshheading:11895479-Nocodazole,
pubmed-meshheading:11895479-Polyploidy,
pubmed-meshheading:11895479-Tumor Cells, Cultured,
pubmed-meshheading:11895479-Vincristine
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pubmed:year |
2002
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pubmed:articleTitle |
Hyperploidy induced by drugs that inhibit formation of microtubule promotes chromosome instability.
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pubmed:affiliation |
Department of Tumor Genetics and Biology, Kumamoto University School of Medicine, 2-2-1 Honjo, Kumamoto 860-0811, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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