Landscape of chromosomal copy number aberrations in gangliogliomas and dysembryoplastic neuroepithelial tumours

被引:33
作者
Prabowo, A. S. [1 ]
van Thuijl, H. F. [5 ,6 ]
Scheinin, I. [6 ,13 ,14 ,15 ]
Sie, D. [6 ]
van Essen, H. F. [6 ]
Iyer, A. M. [1 ]
Spliet, W. G. M. [7 ]
Ferrier, C. H. [8 ,10 ]
van Rijen, P. C. [8 ]
Veersema, T. J. [8 ,9 ]
Thom, M. [16 ]
Schouten-van Meeteren, A. Y. N. [2 ]
Reijneveld, J. C. [3 ,5 ]
Ylstra, B. [6 ]
Wesseling, P. [6 ,11 ]
Aronica, E. [1 ,4 ,12 ]
机构
[1] Univ Amsterdam, Emma Childrens Hosp, Dept Neuropathol, Amsterdam, Netherlands
[2] Univ Amsterdam, Emma Childrens Hosp, Dept Paediat Oncol, Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
[4] Univ Amsterdam, Ctr Neurosci, Swammerdam Inst Life Sci, Amsterdam, Netherlands
[5] Vrije Univ Amsterdam Med Ctr, Dept Neurol, Amsterdam, Netherlands
[6] Vrije Univ Amsterdam Med Ctr, Dept Pathol, Amsterdam, Netherlands
[7] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[8] Univ Med Ctr Utrecht, Dept Neurosurg, Utrecht, Netherlands
[9] Univ Med Ctr Utrecht, Dept Neurol, Utrecht, Netherlands
[10] Univ Med Ctr Utrecht, Dept Clin Neurophysiol, Rudolf Magnus Inst Neurosci, Utrecht, Netherlands
[11] Radboud Univ Nijmegen, Dept Pathol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[12] Stichting Epilepsie Inst Nederland, Heemstede, Netherlands
[13] Univ Helsinki, Dept Pathol, Haartman Inst, Helsinki, Finland
[14] Univ Helsinki, HUSLAB, Helsinki, Finland
[15] Univ Helsinki, Cent Hosp, Helsinki, Finland
[16] UCL, Dept Neuropathol, Inst Neurol, London, England
关键词
copy number aberrations; dysembryoplastic neuroepithelial tumour; ganglioglioma; long-term epilepsy-associated tumours; whole genome sequencing; BRAF(V600E) MUTATION; TRANSCRIPTION FACTOR; EXPRESSION; GLIOMA; CHROMOTHRIPSIS; DIFFUSE; CELLS; REARRANGEMENTS; EVOLUTION; REVEALS;
D O I
10.1111/nan.12235
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim: Gangliogliomas (GGs) and dysembryoplastic neuroepithelial tumours (DNTs) represent the most common histological entities within the spectrum of glioneuronal tumours (GNTs). The wide variability of morphological features complicates histological classification, including discrimination from prognostically distinct diffuse low-grade astrocytomas (AIIs). This study was performed to increase our understanding of these tumours. Methods: We studied chromosomal copy number aberrations(CNAs) by genome-wide sequencing in a large cohort of GNTs and linked these to comprehensive histological analysis and clinical characteristics. One hundred fourteen GNTs were studied: 50GGs and 64DNTs. Also, a data set of CNAs from 38 diffuse AIIs was included. Results: The most frequent CNAs in both GGs and DNTs were gains at chromosomes 5 and 7, often concurrent, and gain at chromosome 6. None of the CNAs was linked to histological subtype, immunohistochemical features or to clinical characteristics. Comparison of AIIs and diffuse GNTs revealed that gain at whole chromosome 5 is only observed in GNTs. CNA patterns indicative of chromothripsis were detected in three GNTs. Conclusion: We conclude that GNTs with diverse morphologies share molecular features, and our findings support the need to improve classification and differential diagnosis of tumour entities within the spectrum of GNTs, as well as their distinction from other gliomas.
引用
收藏
页码:743 / 755
页数:13
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