Abstract
In the present study, we evidence how in breast cancer cells low doses of Taxol for 18 h determined the upregulation of p53 and p21 waf expression concomitantly with a decrease of the anti-apoptotic Bcl-2. P53 and its gene product, the mdm2 protein, in treated cells exhibits a prevalent nuclear compartmentalization, thus potentiating p53 transactivatory properties. Indeed, the most important finding of this study consists with the evidence that Taxol at lower concentrations is able to produce the activation of p21 promoter via p53. Prolonged exposure of MCF-7 cells to Taxol (48 h) resulted in an increased co-association between p21 and PCNA compared to control and this well fits with the simultaneous block of cell cycle into the G2/M phase.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Retracted Publication
MeSH terms
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Active Transport, Cell Nucleus / drug effects
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Antineoplastic Agents, Phytogenic / pharmacology*
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Breast Neoplasms / metabolism*
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Cell Division / drug effects
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Cell Line, Tumor
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Cell Nucleus / metabolism
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Cyclin-Dependent Kinase Inhibitor p21 / metabolism*
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Dose-Response Relationship, Drug
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Female
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G2 Phase / drug effects
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Humans
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Paclitaxel / pharmacology*
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Proliferating Cell Nuclear Antigen / metabolism
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Promoter Regions, Genetic / drug effects
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Protein Binding / drug effects
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Proto-Oncogene Proteins c-bcl-2 / metabolism*
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Proto-Oncogene Proteins c-mdm2 / metabolism
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Time Factors
Substances
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Antineoplastic Agents, Phytogenic
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CDKN1A protein, human
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Cyclin-Dependent Kinase Inhibitor p21
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Proliferating Cell Nuclear Antigen
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Proto-Oncogene Proteins c-bcl-2
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MDM2 protein, human
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Proto-Oncogene Proteins c-mdm2
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Paclitaxel