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Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma

Vimentin is currently used to differentiate between malignant renal carcinomas and benign oncocytomas. Recent reports showing Vimentin positive oncocytomas seriously question the validity of this present diagnostic approach. Vimentin 3 is a spliced variant and ends with a unique C-terminal ending af...

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Autores principales: von Brandenstein, Melanie, Puetz, Katharina, Schlosser, Monika, Löser, Heike, Kallinowski, Joachim P., Gödde, Daniel, Buettner, Reinhard, Störkel, Stefan, Fries, Jochen W. U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405285/
https://www.ncbi.nlm.nih.gov/pubmed/25944973
http://dx.doi.org/10.1155/2015/368534
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author von Brandenstein, Melanie
Puetz, Katharina
Schlosser, Monika
Löser, Heike
Kallinowski, Joachim P.
Gödde, Daniel
Buettner, Reinhard
Störkel, Stefan
Fries, Jochen W. U.
author_facet von Brandenstein, Melanie
Puetz, Katharina
Schlosser, Monika
Löser, Heike
Kallinowski, Joachim P.
Gödde, Daniel
Buettner, Reinhard
Störkel, Stefan
Fries, Jochen W. U.
author_sort von Brandenstein, Melanie
collection PubMed
description Vimentin is currently used to differentiate between malignant renal carcinomas and benign oncocytomas. Recent reports showing Vimentin positive oncocytomas seriously question the validity of this present diagnostic approach. Vimentin 3 is a spliced variant and ends with a unique C-terminal ending after exon 7 which differentiates it from the full length version that has 9 exons. Therefore, the protein size is different; the full length Vimentin version has a protein size of ~57 kDa and the truncated version of ~47 kDa. We designed an antibody, called Vim3, against the unique C-terminal ending of the Vimentin 3 variant. Using immune histology, immune fluorescence, Western blot, and qRT-PCR analysis, a Vim3 overexpression was detectable exclusively in oncocytoma, making the detection of Vim3 a potential specific marker for benign kidney tumors. This antibody is the first to clearly differentiate benign oncocytoma and the mimicking eosinophilic variants of the RCCs. This differentiation between malignant and benign RCCs is essential for operative planning, follow-up therapy, and patients' survival. In the future the usage of Vimentin antibodies in routine pathology has to be applied with care. Consideration must be given to Vimentin specific binding epitopes otherwise a misdiagnosis of the patients' tumor samples may result.
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spelling pubmed-44052852015-05-05 Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma von Brandenstein, Melanie Puetz, Katharina Schlosser, Monika Löser, Heike Kallinowski, Joachim P. Gödde, Daniel Buettner, Reinhard Störkel, Stefan Fries, Jochen W. U. Dis Markers Research Article Vimentin is currently used to differentiate between malignant renal carcinomas and benign oncocytomas. Recent reports showing Vimentin positive oncocytomas seriously question the validity of this present diagnostic approach. Vimentin 3 is a spliced variant and ends with a unique C-terminal ending after exon 7 which differentiates it from the full length version that has 9 exons. Therefore, the protein size is different; the full length Vimentin version has a protein size of ~57 kDa and the truncated version of ~47 kDa. We designed an antibody, called Vim3, against the unique C-terminal ending of the Vimentin 3 variant. Using immune histology, immune fluorescence, Western blot, and qRT-PCR analysis, a Vim3 overexpression was detectable exclusively in oncocytoma, making the detection of Vim3 a potential specific marker for benign kidney tumors. This antibody is the first to clearly differentiate benign oncocytoma and the mimicking eosinophilic variants of the RCCs. This differentiation between malignant and benign RCCs is essential for operative planning, follow-up therapy, and patients' survival. In the future the usage of Vimentin antibodies in routine pathology has to be applied with care. Consideration must be given to Vimentin specific binding epitopes otherwise a misdiagnosis of the patients' tumor samples may result. Hindawi Publishing Corporation 2015 2015-04-07 /pmc/articles/PMC4405285/ /pubmed/25944973 http://dx.doi.org/10.1155/2015/368534 Text en Copyright © 2015 Melanie von Brandenstein et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
von Brandenstein, Melanie
Puetz, Katharina
Schlosser, Monika
Löser, Heike
Kallinowski, Joachim P.
Gödde, Daniel
Buettner, Reinhard
Störkel, Stefan
Fries, Jochen W. U.
Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title_full Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title_fullStr Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title_full_unstemmed Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title_short Vimentin 3, the New Hope, Differentiating RCC versus Oncocytoma
title_sort vimentin 3, the new hope, differentiating rcc versus oncocytoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405285/
https://www.ncbi.nlm.nih.gov/pubmed/25944973
http://dx.doi.org/10.1155/2015/368534
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