Journal Article

DKFZ-2023-00608

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Pediatric-type high-grade neuroepithelial tumors with CIC gene fusion share a common DNA methylation signature.

Sievers, P. (First author)DKFZ* ; Sill, M.DKFZ* ; Schrimpf, D.DKFZ* ; Abdullaev, Z. ; Donson, A. M. ; Lake, J. A. ; Friedel, D.DKFZ* ; Scheie, D. ; Tynninen, O. ; Rauramaa, T. ; Vepsäläinen, K. L. ; Samuel, D. ; Chapman, R. ; Grundy, R. G. ; Pajtler, K. W.DKFZ* ; Tauziède-Espariat, A. ; Métais, A. ; Varlet, P. ; Snuderl, M. ; Jacques, T. S. ; Aldape, K. ; Reuss, D. E.DKFZ* ; Korshunov, A.DKFZ* ; Wick, W.DKFZ* ; Pfister, S. M.DKFZ* ; von Deimling, A.DKFZ* ; Sahm, F. (Last author)DKFZ* ; Jones, D. (Last author)DKFZ*

2023
Springer Nature [London]

This record in other databases:  

Please use a persistent id in citations: doi:10.1038/s41698-023-00372-1

Abstract: Pediatric neoplasms in the central nervous system (CNS) show extensive clinical and molecular heterogeneity and are fundamentally different from those occurring in adults. Molecular genetic testing contributes to accurate diagnosis and enables an optimal clinical management of affected children. Here, we investigated a rare, molecularly distinct type of pediatric high-grade neuroepithelial tumor (n = 18), that was identified through unsupervised visualization of genome-wide DNA methylation array data, together with copy number profiling, targeted next-generation DNA sequencing, and RNA transcriptome sequencing. DNA and/or RNA sequencing revealed recurrent fusions involving the capicua transcriptional repressor (CIC) gene in 10/10 tumor samples analyzed, with the most common fusion being CIC::LEUTX (n = 9). In addition, a CIC::NUTM1 fusion was detected in one of the tumors. Apart from the detected fusion events, no additional oncogenic alteration was identified in these tumors. The histopathological review demonstrated a morphologically heterogeneous group of high-grade neuroepithelial tumors with positive immunostaining for markers of glial differentiation in combination with weak and focal expression of synaptophysin, CD56 and CD99. All tumors were located in the supratentorial compartment, occurred during childhood (median age 8.5 years) and typically showed early relapses. In summary, we expand the spectrum of pediatric-type tumors of the CNS by reporting a previously uncharacterized group of rare high-grade neuroepithelial tumors that share a common DNA methylation signature and recurrent gene fusions involving the transcriptional repressor CIC. Downstream functional consequences of the fusion protein CIC::LEUTX and potential therapeutic implications need to be further investigated.

Note: #EA:B300#LA:B300#LA:B360#

---

Contributing Institute(s):

1. KKE Neuropathologie (B300)
2. B062 Pädiatrische Neuroonkologie (B062)
3. KKE Neuroonkologie (B320)
4. Pediatric Glioma (B360)
5. DKTK HD zentral (HD01)

Research Program(s):

1. 312 - Funktionelle und strukturelle Genomforschung (POF4-312) (POF4-312)

Appears in the scientific report 2023

---

Database coverage:
; ; ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DOAJ Seal ; Essential Science Indicators ; Fees ; IF >= 5 ; JCR ; PubMed Central ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection

---