Source:http://linkedlifedata.com/resource/pubmed/id/10403119
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1999-9-24
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pubmed:abstractText |
Little is known about the role of protein-tyrosine phosphatases (PTPs), the cellular counterparts of protein-tyrosine kinases, both for normal growth regulation and for its dysregulation in cancer. The receptor-like PTPalpha (RPTPalpha) may play a positive role in growth regulation and has been shown to be overexpressed in colon carcinoma. An RNA/RNA in situ hybridisation protocol for RPTPalpha as well as RPTPalpha immunohistochemistry was developed to evaluate RPTPalpha expression in oral squamous cell carcinomas (OSCCs) of different histological grade and to reveal the synthetically active cells and their tissue distribution. In well-differentiated OSCC (G1), RPTPalpha mRNA could be detected by in situ hybridisation exclusively in stroma cells (fibro/myofibroblasts and inflammatory cells). A higher histological grade (G2/G3) was associated with an increased number of RPTPalpha-synthesising carcinoma cells haphazardly distributed within invading tumour areas. Consistent results were obtained by immunocytochemistry. Thus, both carcinoma dedifferentiation and stroma recruitment and activation seem to be associated with an upregulation of RPTPalpha expression in OSCC. The results speak in favour of the important role of activation of stroma fibro/myofibroblasts influencing the biological behaviour of epithelial tumours and also suggest that elevated RPTPalpha expression may be a more general marker for proliferating or dedifferentiated cells.
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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/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PTPRA protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor-Like Protein Tyrosine...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0948-6143
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
399-403
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:10403119-Carcinoma, Squamous Cell,
pubmed-meshheading:10403119-Gene Expression,
pubmed-meshheading:10403119-Humans,
pubmed-meshheading:10403119-Immunoenzyme Techniques,
pubmed-meshheading:10403119-In Situ Hybridization,
pubmed-meshheading:10403119-Membrane Proteins,
pubmed-meshheading:10403119-Mouth Neoplasms,
pubmed-meshheading:10403119-Protein Tyrosine Phosphatases,
pubmed-meshheading:10403119-RNA,
pubmed-meshheading:10403119-Receptor-Like Protein Tyrosine Phosphatases, Class 4,
pubmed-meshheading:10403119-Receptors, Cell Surface,
pubmed-meshheading:10403119-Tumor Cells, Cultured,
pubmed-meshheading:10403119-U937 Cells
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pubmed:year |
1999
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pubmed:articleTitle |
Expression of the transmembrane protein tyrosine phosphatase RPTPalpha in human oral squamous cell carcinoma.
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pubmed:affiliation |
Institute of Pathology, Friedrich Schiller University, Jena, Germany. berndt@bach.med.uni-jena.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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