Source:http://linkedlifedata.com/resource/pubmed/id/20371980
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0034693,
umls-concept:C0193504,
umls-concept:C0205263,
umls-concept:C0221198,
umls-concept:C0229671,
umls-concept:C0334094,
umls-concept:C0380162,
umls-concept:C0441889,
umls-concept:C1138408,
umls-concept:C1171362,
umls-concept:C1378703,
umls-concept:C1515670,
umls-concept:C1979925
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pubmed:issue |
2
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pubmed:dateCreated |
2010-4-7
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pubmed:abstractText |
Expressed in renal carcinoma (ERC)/mesothelin is a good biomarker for human mesothelioma and has been investigated for its mechanistic rationale during the mesothelioma development. Studies are thus ongoing in our laboratories to assess expression of ERC/mesothelin in sera and normal/proliferative/neoplastic mesothelial tissues of animals untreated or given potentially mesothelioma-inducible xenobiotics, by an enzyme-linked immunosorbent assay (ELISA) for N- and C-(terminal fragments of) ERC/mesothelin and immunohistochemistry for C-ERC/mesothelin. In the present paper, we intend to communicate our preliminary data, because this is the first report to show how and from what stage the ERC/mesothelin expression changes during the chemical induction of mesothelial proliferative/neoplatic lesions. Serum N-ERC/mesothelin levels were 51.4 +/- 5.6 ng/ml in control male Fischer 344 rats, increased to 83.6 +/- 11.2 ng/ml in rats given a single intrascrotal administration of 1 mg/kg body weight of multi-wall carbon nanotube (MWCNT) and bearing mesothelial hyperplasia 52 weeks thereafter, and further elevated to 180 +/- 77 ng/ml in rats similarly treated and becoming moribund 40 weeks thereafter, or killed as scheduled at the end of week 52, bearing mesothelioma. While C-ERC/mesothelin was expressed in normal and hyperplastic mesothelia, the protein was detected only in epithelioid mesothelioma cells at the most superficial layer. It is thus suggested that ERC/mesothelin can be used as a biomarker of mesothelial proliferative lesions also in animals, and that the increase of levels may start from the early stage and be enhanced by the progression of the mesothelioma development.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1880-3989
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pubmed:author |
pubmed-author:FukamachiKatsumiK,
pubmed-author:HagiwaraYoshiakiY,
pubmed-author:HinoOkioO,
pubmed-author:HiroseAkihikoA,
pubmed-author:NakaeDaiD,
pubmed-author:NishimuraTetsujiT,
pubmed-author:OgataAkioA,
pubmed-author:OhashiNorioN,
pubmed-author:SakamotoYoshimitsuY,
pubmed-author:SatohKanakoK,
pubmed-author:TsudaHiroyukiH
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pubmed:issnType |
Electronic
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
265-70
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pubmed:dateRevised |
2011-10-26
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pubmed:meshHeading |
pubmed-meshheading:20371980-Animals,
pubmed-meshheading:20371980-Cell Proliferation,
pubmed-meshheading:20371980-Epithelium,
pubmed-meshheading:20371980-GPI-Linked Proteins,
pubmed-meshheading:20371980-Male,
pubmed-meshheading:20371980-Membrane Glycoproteins,
pubmed-meshheading:20371980-Nanotubes, Carbon,
pubmed-meshheading:20371980-Rats,
pubmed-meshheading:20371980-Rats, Inbred F344
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pubmed:year |
2010
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pubmed:articleTitle |
Serum level of expressed in renal carcinoma (ERC)/ mesothelin in rats with mesothelial proliferative lesions induced by multi-wall carbon nanotube (MWCNT).
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pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
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