Source:http://linkedlifedata.com/resource/pubmed/id/16943690
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-8-31
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pubmed:abstractText |
According to a good correlation between in situ hybridization-based metalloproteinase-2/9:E-cadherin ratio (MER) and the pathological stage of prostate cancer, we set the cutoff line of MER at 6.0 (MER>6) to distinguish between organ-confined (pT2) and advanced diseases (pT3a-b/N1). In this study, we looked at the factors affecting MER and leading to a misprediction of the pathological stage. We examined MER in 39 paired specimens of prostate core needle biopsy and prostatectomy from the same patient and compared these MERs. In 34 (87%) of 39 cases, the MER of biopsy was correlated with the final pathological stage (pT2 vs. pT3a-b/N1). MER ranges in pT3a-b/N1 cancer were significantly wider than those in pT2 cancer (p < 0.01). The number of MER>6 fields in Gleason score 8-9 cancer was larger than that in Gleason score 7 cancer (p < 0.0001). In 5 cases where there was a failure to distinguish pT2 from pT3a-b/N1, the misdiagnosis was significantly associated with a small number of biopsies (4 or 6 specimens; p = 0.0469), a small amount of tumor tissue in biopsy specimens (less than 5 mm; p = 0.0492), and a wide MER range (more than 5.0; high intratumoral heterogeneity; p = 0.0202). Considering these factors increases the usefulness of preoperative prediction of the final pathological stage by MER in prostate cancer.
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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/Cadherins,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 9,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Markers, Biological
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pubmed:status |
MEDLINE
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pubmed:issn |
1015-2008
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2006 S. Karger AG, Basel.
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pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
98-104
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16943690-Biopsy, Needle,
pubmed-meshheading:16943690-Cadherins,
pubmed-meshheading:16943690-Disease Progression,
pubmed-meshheading:16943690-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:16943690-Humans,
pubmed-meshheading:16943690-Male,
pubmed-meshheading:16943690-Matrix Metalloproteinase 2,
pubmed-meshheading:16943690-Matrix Metalloproteinase 9,
pubmed-meshheading:16943690-Neoplasm Staging,
pubmed-meshheading:16943690-Predictive Value of Tests,
pubmed-meshheading:16943690-Prognosis,
pubmed-meshheading:16943690-Prostatic Neoplasms,
pubmed-meshheading:16943690-RNA, Messenger,
pubmed-meshheading:16943690-Reference Values,
pubmed-meshheading:16943690-Tumor Markers, Biological
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pubmed:year |
2006
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pubmed:articleTitle |
Determinants for prediction of malignant potential by metalloproteinase:E-cadherin ratio in prostate core needle biopsy.
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pubmed:affiliation |
Department of Molecular Pathology, Nara Medical University School of Medicine, Kashihara, Japan.
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pubmed:publicationType |
Journal Article,
Evaluation Studies
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