Source:http://linkedlifedata.com/resource/pubmed/id/14647039
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2003-12-3
|
pubmed:abstractText |
Calcifying epithelial odontogenic tumors (CEOTs), also known as Pindborg tumors, are characterized by the presence of squamous-cell proliferation, calcification, and, notably, amyloid deposits. On the basis of immunohistochemical analyses, the amyloidogenic component had heretofore been deemed to consist of cytokeratin-related or other molecules; however, its chemical composition had never been elucidated. We have used our microanalytic techniques to characterize the protein nature of CEOT-associated amyloid isolated from specimens obtained from 3 patients. As evidenced by the results of amino-acid sequencing and mass spectrometry, the fibrils were found to be composed of a polypeptide of approximately 46 mer. This component was identical in sequence to the N-terminal portion of a hypothetical 153-residue protein encoded by the FLJ20513 gene cloned from the human KATO III cell line. That the amyloid protein was derived from this larger molecule was demonstrated by reverse transcription-polymerase chain reaction amplification of tumor-cell RNA where a full-length FLJ20513 transcript was found. Furthermore, immunohistochemical analyses revealed that the amyloid within the CEOTs immunostained with antibodies prepared against a synthetic FLJ20513-related dodecapeptide. Our studies provide unequivocal evidence that CEOT-associated amyloid consists of a unique and previously undescribed protein that we provisionally designate APin.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0022-2143
|
pubmed:author |
pubmed-author:DonnellRobert LRL,
pubmed-author:EulitzManfredM,
pubmed-author:HrncicRudiR,
pubmed-author:MurphyCharles LCL,
pubmed-author:SlettenKnutK,
pubmed-author:SolomonAlanA,
pubmed-author:WeaverKristalK,
pubmed-author:WeissDeborah TDT,
pubmed-author:WestermarkGunillaG,
pubmed-author:WestermarkPerP
|
pubmed:issnType |
Print
|
pubmed:volume |
142
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
348-55
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:14647039-Adolescent,
pubmed-meshheading:14647039-Amino Acid Sequence,
pubmed-meshheading:14647039-Amyloid,
pubmed-meshheading:14647039-Amyloidosis,
pubmed-meshheading:14647039-Antibodies,
pubmed-meshheading:14647039-Cloning, Molecular,
pubmed-meshheading:14647039-Female,
pubmed-meshheading:14647039-Humans,
pubmed-meshheading:14647039-Immunohistochemistry,
pubmed-meshheading:14647039-Jaw Neoplasms,
pubmed-meshheading:14647039-Middle Aged,
pubmed-meshheading:14647039-Molecular Sequence Data,
pubmed-meshheading:14647039-Neoplasm Proteins,
pubmed-meshheading:14647039-Odontogenic Cyst, Calcifying
|
pubmed:year |
2003
|
pubmed:articleTitle |
Calcifying epithelial odontogenic (Pindborg) tumor-associated amyloid consists of a novel human protein.
|
pubmed:affiliation |
Human Immunology and Cancer Program, Department of Medicine, University of Tennessee Graduate School of Medicine, Knoxville 37920, USA. asolomon@mc.utmck.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|