Source:http://linkedlifedata.com/resource/pubmed/id/10754496
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2000-4-27
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pubmed:abstractText |
Expression of the telomerase catalytic sub-unit (htert) constitutes a key step in the development of human cancer. Although htert regulation is still unclear, several studies suggest that c-myc may activate its expression. Prostate cancer is one of the most common malignancies among men in Western countries. Since de-regulated expression of myc as well as telomerase activation may contribute to the pathogenicity of this cancer, we investigated this pathway in prostate tumorigenesis. For this purpose, myc- and htert-mRNA expression was quantified in 33 sporadic prostate tumors using a real-time quantitative PCR assay based on TaqMan methodology. myc over-expression was observed in 19 (58%) of 33 tumors, whereas telomerase status evaluated by htert expression was observed in 22 (67%). There was no correlation between myc over-expression or htert expression level and tumor stage or Gleason grade. A significant association (p = 0.0024) was found between myc over-expression and elevated htert expression, indicating that the up-regulation of telomerase activity often observed in prostate tumors might be conferred through transactivation of htert by myc. It is likely that the ability of c-myc protein to stimulate expression of htert and thereby enhance telomerase activity represents an important step in prostate tumorigenesis.
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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/DNA, Neoplasm,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Oligonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc,
http://linkedlifedata.com/resource/pubmed/chemical/RNA,
http://linkedlifedata.com/resource/pubmed/chemical/Telomerase,
http://linkedlifedata.com/resource/pubmed/chemical/telomerase RNA
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2000 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
89
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
172-6
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pubmed:dateRevised |
2007-7-24
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pubmed:meshHeading |
pubmed-meshheading:10754496-DNA, Neoplasm,
pubmed-meshheading:10754496-DNA Primers,
pubmed-meshheading:10754496-DNA-Binding Proteins,
pubmed-meshheading:10754496-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:10754496-Genes, myc,
pubmed-meshheading:10754496-Humans,
pubmed-meshheading:10754496-Male,
pubmed-meshheading:10754496-Oligonucleotides,
pubmed-meshheading:10754496-Prostatic Neoplasms,
pubmed-meshheading:10754496-Proto-Oncogene Proteins c-myc,
pubmed-meshheading:10754496-RNA,
pubmed-meshheading:10754496-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:10754496-Specimen Handling,
pubmed-meshheading:10754496-Telomerase,
pubmed-meshheading:10754496-Tumor Cells, Cultured,
pubmed-meshheading:10754496-Up-Regulation
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pubmed:year |
2000
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pubmed:articleTitle |
htert expression correlates with MYC over-expression in human prostate cancer.
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pubmed:affiliation |
Laboratoire d'Oncogénétique, Centre René Huguenin, St-Cloud, France.
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pubmed:publicationType |
Journal Article
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