Source:http://linkedlifedata.com/resource/pubmed/id/18413812
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2008-4-16
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pubmed:abstractText |
Nutlin-3 is a small-molecule inhibitor that acts to inhibit MDM2 binding to p53 and subsequent p53-dependent DNA damage signaling. Whether Nutlin-3 alters cell toxicity following DNA damage under oxic versus hypoxic conditions has not been studied. The potential radiosensitization (0-10 Gy) properties of Nutlin-3 (dose range, 2-10 micromol/L for up to 24 h) were investigated in vitro using three prostate cancer cell lines, 22RV1 [wild-type p53 (WTp53)], DU145 (mutated p53), and PC-3 (p53-null) under oxic (21% O(2)), hypoxic (0.2% O(2)), and anoxic (0% O(2)) conditions. As a single agent, Nutlin-3 (2-10 micromol/L) stabilized p53 and p21(WAF) levels and was toxic to WTp53-22RV1 cells (IC(50), 4.3 micromol/L) but had minimal toxicity toward p53-deficient cells (IC(50), >10 micromol/L). When combined with radiation under oxic conditions, Nutlin-3 decreased clonogenic survival in all three cell lines: 22RV1 [sensitizing enhancement ratio (SER), 1.24], DU145 (SER, 1.27), and PC-3 (SER, 1.12). Anoxia induced p53 protein expression in 22RV1 cells and this was augmented by Nutlin-3 treatment. Furthermore, Nutlin-3 was more effective as a radiosensitizer under hypoxic conditions particularly in WTp53-expressing cells: 22RV1 (SER, 1.78), DU145 (SER, 1.31), and PC-3 (SER, 1.28). The decrease in clonogenic survival with Nutlin-3 was not correlated to altered levels of radiation-induced apoptosis within the three cell lines. Our results indicate that Nutlin-3 can act as a radiosensitizer via p53-independent mechanisms under low O(2) levels. Nutlin-3 may be a useful adjunct to improve the therapeutic ratio using precision radiotherapy targeted to hypoxic cells and warrants further study in vivo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/HIF1A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoxia-Inducible Factor 1, alpha...,
http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/MDM2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-mdm2,
http://linkedlifedata.com/resource/pubmed/chemical/Radiation-Sensitizing Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53,
http://linkedlifedata.com/resource/pubmed/chemical/nutlin 3
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1535-7163
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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 |
993-9
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pubmed:meshHeading |
pubmed-meshheading:18413812-Anoxia,
pubmed-meshheading:18413812-Apoptosis,
pubmed-meshheading:18413812-Blotting, Western,
pubmed-meshheading:18413812-Caspases,
pubmed-meshheading:18413812-Cell Cycle,
pubmed-meshheading:18413812-Humans,
pubmed-meshheading:18413812-Hypoxia-Inducible Factor 1, alpha Subunit,
pubmed-meshheading:18413812-Imidazoles,
pubmed-meshheading:18413812-Male,
pubmed-meshheading:18413812-Piperazines,
pubmed-meshheading:18413812-Prostatic Neoplasms,
pubmed-meshheading:18413812-Proto-Oncogene Proteins c-mdm2,
pubmed-meshheading:18413812-Radiation-Sensitizing Agents,
pubmed-meshheading:18413812-Stereoisomerism,
pubmed-meshheading:18413812-Tumor Cells, Cultured,
pubmed-meshheading:18413812-Tumor Stem Cell Assay,
pubmed-meshheading:18413812-Tumor Suppressor Protein p53
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pubmed:year |
2008
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pubmed:articleTitle |
Nutlin-3 radiosensitizes hypoxic prostate cancer cells independent of p53.
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pubmed:affiliation |
Princess Margaret Hospital (University Health Network), Department of Medical Biophysics, University of Toronto, 610 University Avenue, Toronto, Ontario, Canada M5G 2M9.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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