Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Thimsen, Vivian, Hölsken, Annett, Buchfelder, Michael, Flitsch, Jörg, Fahlbusch, Rudolf, Stefanits, Harald, Losa, Marco, Jones, David T. W., Buslei, Rolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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
_version_ 1782443434680778752
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
work_keys_str_mv AT thimsenvivian epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT holskenannett epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT buchfeldermichael epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT flitschjorg epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT fahlbuschrudolf epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT stefanitsharald epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT losamarco epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT jonesdavidtw epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts
AT busleirolf epcamcd326isdifferentiallyexpressedincraniopharyngiomasubtypesandrathkescleftcysts