Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression
- PMID: 23371454
- DOI: 10.1007/s11060-013-1062-1
Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression
Abstract
Ependymomas comprise 8 % of all intracranial tumors in children <15 years. Recent studies revealed that some supratentorial ependymomas express neuronal antigens and that high expression of neurofilament protein light polypeptide (NEFL) correlates with better clinical outcome. We retrospectively analyzed an expanded panel of proteins in 6 supratentorial, 15 posterior fossa and 4 spinal pediatric ependymomas by immunohistochemistry. Expression of high and low affinity neurotrophin receptors TrkA (NTRK1) and p75 (NGFR), pan-neuronal markers NeuN (RBFOX3) and synaptophysin, radial glial marker SOX9, adhesion molecules CD56 (NCAM) and CD44, junctional protein connexin 43 (GJA1), glial fibrillary acidic protein (GFAP), epithelial membrane antigen and proliferation associated antigen Ki-67 were evaluated in a semi-quantitative or quantitative (Ki-67 and NeuN-index) fashion. We found p75 and NeuN to be expressed at significantly higher levels in supratentorial versus infratentorial tumors and GFAP to be expressed at significantly higher levels in infratentorial lesions. In conclusion, immunohistochemical expression of p75, NeuN and GFAP differed in ependymomas depending on tumor topography supporting the view of divergent cells of origin. However, because of the small sample size the results are of preliminary nature and replication in a larger cohort would be desirable.
Similar articles
-
Neuronal differentiation distinguishes supratentorial and infratentorial childhood ependymomas.Neuro Oncol. 2010 Nov;12(11):1126-34. doi: 10.1093/neuonc/noq074. Epub 2010 Jul 8. Neuro Oncol. 2010. PMID: 20615923 Free PMC article.
-
Prognostic value of H3K27me3 in children with ependymoma.Pediatr Blood Cancer. 2020 Mar;67(3):e28121. doi: 10.1002/pbc.28121. Epub 2019 Dec 18. Pediatr Blood Cancer. 2020. PMID: 31850684
-
Chromosome 1q gain and tenascin-C expression are candidate markers to define different risk groups in pediatric posterior fossa ependymoma.Acta Neuropathol Commun. 2016 Aug 22;4(1):88. doi: 10.1186/s40478-016-0349-9. Acta Neuropathol Commun. 2016. PMID: 27550150 Free PMC article.
-
Supratentorial and Infratentorial Ependymoma.Adv Tech Stand Neurosurg. 2024;53:93-118. doi: 10.1007/978-3-031-67077-0_7. Adv Tech Stand Neurosurg. 2024. PMID: 39287805 Review.
-
Intracranial ependymomas: molecular insights and translation to treatment.Brain Pathol. 2020 Jan;30(1):3-12. doi: 10.1111/bpa.12781. Epub 2019 Sep 12. Brain Pathol. 2020. PMID: 31433520 Free PMC article. Review.
Cited by
-
NeuN As a Neuronal Nuclear Antigen and Neuron Differentiation Marker.Acta Naturae. 2015 Apr-Jun;7(2):42-7. Acta Naturae. 2015. PMID: 26085943 Free PMC article.
-
Neuronal Activity in Ontogeny and Oncology.Trends Cancer. 2017 Feb;3(2):89-112. doi: 10.1016/j.trecan.2016.12.008. Epub 2017 Feb 13. Trends Cancer. 2017. PMID: 28718448 Free PMC article. Review.
-
Neurotrophin Signaling in Medulloblastoma.Cancers (Basel). 2020 Sep 7;12(9):2542. doi: 10.3390/cancers12092542. Cancers (Basel). 2020. PMID: 32906676 Free PMC article. Review.
-
Prognostic and microRNA profile analysis for CD44 positive expression pediatric posterior fossa ependymoma.Clin Transl Oncol. 2018 Nov;20(11):1439-1447. doi: 10.1007/s12094-018-1876-6. Epub 2018 Apr 27. Clin Transl Oncol. 2018. PMID: 29704232
-
Proteomic and Mitochondrial Genomic Analyses of Pediatric Brain Tumors.Mol Neurobiol. 2015 Dec;52(3):1341-1363. doi: 10.1007/s12035-014-8930-3. Epub 2014 Oct 25. Mol Neurobiol. 2015. PMID: 25341474
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous