Source:http://linkedlifedata.com/resource/pubmed/id/10421546
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1999-7-29
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pubmed:abstractText |
The antitumor agent paclitaxel (Taxol) has been shown to arrest cells in mitosis through microtubule stabilization and to induce apoptosis. The tumor suppressor gene p53 is implicated in the regulation of cell cycle checkpoints and can mediate apoptotic cell death. Although initial studies demonstrated that various DNA-damaging agents can induce p53, more recent studies have also shown p53 induction following nonDNA-damaging agents, including paclitaxel. We investigated the influence of p53 abrogation on paclitaxel-induced cell kill and correlated the extent of mitotic arrest and DNA fragmentation by paclitaxel with the drug's cytotoxic effect.
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pubmed:grant | |
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 |
Jul
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pubmed:issn |
0360-3016
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
44
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1119-24
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10421546-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:10421546-DNA, Neoplasm,
pubmed-meshheading:10421546-DNA Fragmentation,
pubmed-meshheading:10421546-Dose-Response Relationship, Drug,
pubmed-meshheading:10421546-Drug Resistance,
pubmed-meshheading:10421546-Genes, p53,
pubmed-meshheading:10421546-Humans,
pubmed-meshheading:10421546-Micronuclei, Chromosome-Defective,
pubmed-meshheading:10421546-Paclitaxel,
pubmed-meshheading:10421546-Tumor Cells, Cultured,
pubmed-meshheading:10421546-Tumor Stem Cell Assay
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pubmed:year |
1999
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pubmed:articleTitle |
Paclitaxel sensitivity correlates with p53 status and DNA fragmentation, but not G2/M accumulation.
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pubmed:affiliation |
Center for Radiological Research, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
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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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