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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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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. |
format | Online Article Text |
id | pubmed-4405285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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