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EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts
The epithelial cell adhesion molecule (EpCAM) is a type I glycoprotein located on the surface of epithelial cells. It is strongly expressed in many neoplasms and already used in the diagnosis and distinction of various tumour subtypes. Comparative studies about EpCAM expression in cystic sellar lesi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949472/ https://www.ncbi.nlm.nih.gov/pubmed/27431859 http://dx.doi.org/10.1038/srep29731 |
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author | Thimsen, Vivian Hölsken, Annett Buchfelder, Michael Flitsch, Jörg Fahlbusch, Rudolf Stefanits, Harald Losa, Marco Jones, David T. W. Buslei, Rolf |
author_facet | Thimsen, Vivian Hölsken, Annett Buchfelder, Michael Flitsch, Jörg Fahlbusch, Rudolf Stefanits, Harald Losa, Marco Jones, David T. W. Buslei, Rolf |
author_sort | Thimsen, Vivian |
collection | PubMed |
description | The epithelial cell adhesion molecule (EpCAM) is a type I glycoprotein located on the surface of epithelial cells. It is strongly expressed in many neoplasms and already used in the diagnosis and distinction of various tumour subtypes. Comparative studies about EpCAM expression in cystic sellar lesions are lacking. Therefore, we analysed its distribution pattern in adamantinomatous (aCP) and papillary (pCP) craniopharyngiomas (CP) and Rathke’s Cleft Cysts (RCC) using immunohistochemistry and gene expression profiling. Whereas the protein was not detectable in pCP (n = 10), all aCP (n = 64) showed distinct staining patterns. The vast majority of RCC (n = 10) also appeared positive, but these displayed notably lower labeling scores. Additionally, significantly higher mRNA levels were detectable in aCP (n = 19) when compared to pCP (n = 10) (p = 9.985(−8)). Furthermore, pediatric aCP cases, in general, exhibited stronger EpCAM staining levels compared to adult ones (p = 0.015). However, we were not able to verify this result on mRNA level. In summary, our findings demonstrate that EpCAM can be used as an additional distinction-marker for cystic lesions of the sellar region. Its unknown function in aCP and the presence of an approved monoclonal bispecific trifunctional antibody for cancer therapy are interesting starting points for further studies. |
format | Online Article Text |
id | pubmed-4949472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49494722016-07-26 EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts Thimsen, Vivian Hölsken, Annett Buchfelder, Michael Flitsch, Jörg Fahlbusch, Rudolf Stefanits, Harald Losa, Marco Jones, David T. W. Buslei, Rolf Sci Rep Article The epithelial cell adhesion molecule (EpCAM) is a type I glycoprotein located on the surface of epithelial cells. It is strongly expressed in many neoplasms and already used in the diagnosis and distinction of various tumour subtypes. Comparative studies about EpCAM expression in cystic sellar lesions are lacking. Therefore, we analysed its distribution pattern in adamantinomatous (aCP) and papillary (pCP) craniopharyngiomas (CP) and Rathke’s Cleft Cysts (RCC) using immunohistochemistry and gene expression profiling. Whereas the protein was not detectable in pCP (n = 10), all aCP (n = 64) showed distinct staining patterns. The vast majority of RCC (n = 10) also appeared positive, but these displayed notably lower labeling scores. Additionally, significantly higher mRNA levels were detectable in aCP (n = 19) when compared to pCP (n = 10) (p = 9.985(−8)). Furthermore, pediatric aCP cases, in general, exhibited stronger EpCAM staining levels compared to adult ones (p = 0.015). However, we were not able to verify this result on mRNA level. In summary, our findings demonstrate that EpCAM can be used as an additional distinction-marker for cystic lesions of the sellar region. Its unknown function in aCP and the presence of an approved monoclonal bispecific trifunctional antibody for cancer therapy are interesting starting points for further studies. Nature Publishing Group 2016-07-19 /pmc/articles/PMC4949472/ /pubmed/27431859 http://dx.doi.org/10.1038/srep29731 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Thimsen, Vivian Hölsken, Annett Buchfelder, Michael Flitsch, Jörg Fahlbusch, Rudolf Stefanits, Harald Losa, Marco Jones, David T. W. Buslei, Rolf EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title | EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title_full | EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title_fullStr | EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title_full_unstemmed | EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title_short | EpCAM (CD326) is differentially expressed in craniopharyngioma subtypes and Rathke’s cleft cysts |
title_sort | epcam (cd326) is differentially expressed in craniopharyngioma subtypes and rathke’s cleft cysts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949472/ https://www.ncbi.nlm.nih.gov/pubmed/27431859 http://dx.doi.org/10.1038/srep29731 |
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