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PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups

AIMS: An ependymoma shows divergent morphological and molecular features depending on their location. The paired box 6 (PAX6) transcription factor is a putative tumour suppressor and drives cancer cells towards a stem cell-like state. A transcriptome study reported high PAX6 expression in ependymal...

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Autores principales: Tabasaran, Julian, Schuhmann, Martin, Ebinger, Martin, Honegger, Jürgen, Renovanz, Mirjam, Schittenhelm, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606524/
https://www.ncbi.nlm.nih.gov/pubmed/34183436
http://dx.doi.org/10.1136/jclinpath-2021-207526
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author Tabasaran, Julian
Schuhmann, Martin
Ebinger, Martin
Honegger, Jürgen
Renovanz, Mirjam
Schittenhelm, Jens
author_facet Tabasaran, Julian
Schuhmann, Martin
Ebinger, Martin
Honegger, Jürgen
Renovanz, Mirjam
Schittenhelm, Jens
author_sort Tabasaran, Julian
collection PubMed
description AIMS: An ependymoma shows divergent morphological and molecular features depending on their location. The paired box 6 (PAX6) transcription factor is a putative tumour suppressor and drives cancer cells towards a stem cell-like state. A transcriptome study reported high PAX6 expression in ependymal tumours, but data on protein expression are lacking. METHODS: We, therefore, analysed PAX6 expression by immunohistochemistry in 172 ependymoma samples and correlated its expression to histology, WHO grade, anatomical location and molecular subgroups. RESULTS: Mean PAX6 nuclear expression in ependymoma was 27.5% (95% CI 23.3 to 31.7). PAX6 expression in subependymoma (mean: 5%) was significantly lower compared with myxopapillary (30%), WHO grade II (26%) and anaplastic ependymoma (35%). Supratentorial ependymomas also displayed significant lower PAX6 levels (15%) compared with spinal cord tumours (30%). Expression levels in YAP1-fused ependymoma (41%) were higher compared with REL-associated protein (RELA)-fusion positive tumours (17%), while PAX6 expression was similar in posterior fossa group A (33%) and B (29%) ependymomas. Kaplan-Meier analysis in RELA-fusion positive ependymomas and posterior fossa group B showed a significant better outcome for PAX6 at or above the cut-off of 19.45% compared with tumours with PAX6 below the cut-off. CONCLUSIONS: We demonstrate that PAX6 is frequently expressed in human ependymal tumours and immunohistochemistry may be helpful in determining prognostic relevant subgroups.
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spelling pubmed-96065242022-10-28 PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups Tabasaran, Julian Schuhmann, Martin Ebinger, Martin Honegger, Jürgen Renovanz, Mirjam Schittenhelm, Jens J Clin Pathol Original Research AIMS: An ependymoma shows divergent morphological and molecular features depending on their location. The paired box 6 (PAX6) transcription factor is a putative tumour suppressor and drives cancer cells towards a stem cell-like state. A transcriptome study reported high PAX6 expression in ependymal tumours, but data on protein expression are lacking. METHODS: We, therefore, analysed PAX6 expression by immunohistochemistry in 172 ependymoma samples and correlated its expression to histology, WHO grade, anatomical location and molecular subgroups. RESULTS: Mean PAX6 nuclear expression in ependymoma was 27.5% (95% CI 23.3 to 31.7). PAX6 expression in subependymoma (mean: 5%) was significantly lower compared with myxopapillary (30%), WHO grade II (26%) and anaplastic ependymoma (35%). Supratentorial ependymomas also displayed significant lower PAX6 levels (15%) compared with spinal cord tumours (30%). Expression levels in YAP1-fused ependymoma (41%) were higher compared with REL-associated protein (RELA)-fusion positive tumours (17%), while PAX6 expression was similar in posterior fossa group A (33%) and B (29%) ependymomas. Kaplan-Meier analysis in RELA-fusion positive ependymomas and posterior fossa group B showed a significant better outcome for PAX6 at or above the cut-off of 19.45% compared with tumours with PAX6 below the cut-off. CONCLUSIONS: We demonstrate that PAX6 is frequently expressed in human ependymal tumours and immunohistochemistry may be helpful in determining prognostic relevant subgroups. BMJ Publishing Group 2022-11 2021-06-28 /pmc/articles/PMC9606524/ /pubmed/34183436 http://dx.doi.org/10.1136/jclinpath-2021-207526 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Tabasaran, Julian
Schuhmann, Martin
Ebinger, Martin
Honegger, Jürgen
Renovanz, Mirjam
Schittenhelm, Jens
PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title_full PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title_fullStr PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title_full_unstemmed PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title_short PAX6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
title_sort pax6 is frequently expressed in ependymal tumours and associated with prognostic relevant subgroups
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606524/
https://www.ncbi.nlm.nih.gov/pubmed/34183436
http://dx.doi.org/10.1136/jclinpath-2021-207526
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