Integrated multi-omics analysis of oligodendroglial tumours identifies three subgroups of 1p/19q co-deleted gliomas

被引:0
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作者
Aurélie Kamoun
Ahmed Idbaih
Caroline Dehais
Nabila Elarouci
Catherine Carpentier
Eric Letouzé
Carole Colin
Karima Mokhtari
Anne Jouvet
Emmanuelle Uro-Coste
Nadine Martin-Duverneuil
Marc Sanson
Jean-Yves Delattre
Dominique Figarella-Branger
Aurélien de Reyniès
François Ducray
机构
[1] Programme Cartes d’Identité des Tumeurs (CIT),Département de Pathologie et Neuropathologie
[2] Ligue Nationale Contre Le Cancer,Department of Cancer Cell Plasticity
[3] Université Pierre et Marie Curie Paris 6,Pathology Department
[4] Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM),Pathology Department
[5] UMR 975,Pathology Department
[6] INSERM U975,Neurosurgery Department
[7] CNRS,Neuro
[8] UMR 7225,oncology Department
[9] AP-HP,Neuropathology Department
[10] Groupe Hospitalier Pitié-Salpêtrière,Pathology Department
[11] Service de Neurologie 2-Mazarin,Medical Oncology Department
[12] Université de la Méditerranée,Neurology Department
[13] Aix-Marseille,Medical Oncology Department
[14] Faculté de Médecine La Timone,Neurosurgery Department
[15] CRO2,Pathology Department
[16] UMR 911,Pathology Department
[17] AP-HP,Neuro
[18] Groupe Hospitalier Pitié-Salpêtrière,oncology Department
[19] Laboratoire de Neuropathologie R. Escourolle,Radiotherapy Department
[20] Hôpital Neurologique,Radiotherapy Department
[21] Hospices Civils de Lyon,Neurosurgery Department
[22] CHU Toulouse,Neurosurgery Department
[23] Hôpital de Rangueil,Neurosurgery Department
[24] Service d’Anatomie et Cytologie Pathologique,Radiotherapy Department
[25] AP-HP,Pathology Department
[26] Groupe Hospitalier Pitié-Salpêtrière,Pathology Department
[27] Service de Neuroradiologie,Neurosurgery Department
[28] Onconeurotek,Radiotherapy Department
[29] Groupe Hospitalier Pitié-Salpêtrière,Neurosurgery Department
[30] AP-HM,Neurosurgery Department
[31] Hôpital de la Timone,Pathology Department
[32] Service d’Anatomie Pathologique et de Neuropathologie,Neurology Department
[33] Hospices Civils de Lyon,Neurosurgery Department
[34] Hôpital Neurologique,Neurosurgery Department
[35] Service de Neuro-Oncologie,Neurology Department
[36] Cancer Research Centre of Lyon,Neurosurgery Department
[37] INSERM U1052,Neuro
[38] CNRS UMR5286,oncology Department
[39] Université Claude Bernard Lyon 1,Pathology Department
[40] Hôpital Bicêtre,Neurosurgery Department
[41] CHU Saint-Pierre de la Réunion,Pathology Department
[42] CHU Dijon,Neurosurgery Department
[43] CHU de Montpellier,Pathology Department
[44] CHU Nancy,Neurology Department
[45] Groupe Hospitalier Pitié-Salpêtrière,Pathology Department
[46] CHR Orléans,Neurosurgery Department
[47] Centre René Gauducheau,Neurosurgery Department
[48] Hôpital Avicenne,Neurosurgery Department
[49] Clinique des Cèdres,Pathology Department
[50] Hôpital Beaujon,Pathology Department
来源
Nature Communications | / 7卷
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摘要
Oligodendroglial tumours (OT) are a heterogeneous group of gliomas. Three molecular subgroups are currently distinguished on the basis of the IDH mutation and 1p/19q co-deletion. Here we present an integrated analysis of the transcriptome, genome and methylome of 156 OT. Not only does our multi-omics classification match the current classification but also reveals three subgroups within 1p/19q co-deleted tumours, associated with specific expression patterns of nervous system cell types: oligodendrocyte, oligodendrocyte precursor cell (OPC) and neuronal lineage. We confirm the validity of these three subgroups using public datasets. Importantly, the OPC-like group is associated with more aggressive clinical and molecular patterns, including MYC activation. We show that the MYC activation occurs through various alterations, including MYC genomic gain, MAX genomic loss, MYC hypomethylation and microRNA-34b/c down-regulation. In the lower grade glioma TCGA dataset, the OPC-like group is associated with a poorer outcome independently of histological grade. Our study reveals previously unrecognized heterogeneity among 1p/19q co-deleted tumours.
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