Author
Listed:
- Aurélie Kamoun
(Programme Cartes d’Identité des Tumeurs (CIT), Ligue Nationale Contre Le Cancer)
- Ahmed Idbaih
(Université Pierre et Marie Curie Paris 6, Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM), UMR 975
INSERM U975
CNRS, UMR 7225
AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie 2-Mazarin)
- Caroline Dehais
(AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie 2-Mazarin)
- Nabila Elarouci
(Programme Cartes d’Identité des Tumeurs (CIT), Ligue Nationale Contre Le Cancer)
- Catherine Carpentier
(Université Pierre et Marie Curie Paris 6, Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM), UMR 975
INSERM U975
CNRS, UMR 7225)
- Eric Letouzé
(Programme Cartes d’Identité des Tumeurs (CIT), Ligue Nationale Contre Le Cancer)
- Carole Colin
(Université de la Méditerranée, Aix-Marseille, Faculté de Médecine La Timone, CRO2, UMR 911)
- Karima Mokhtari
(Université Pierre et Marie Curie Paris 6, Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM), UMR 975
INSERM U975
CNRS, UMR 7225
AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Laboratoire de Neuropathologie R. Escourolle)
- Anne Jouvet
(Hôpital Neurologique, Hospices Civils de Lyon)
- Emmanuelle Uro-Coste
(CHU Toulouse, Hôpital de Rangueil, Service d’Anatomie et Cytologie Pathologique)
- Nadine Martin-Duverneuil
(AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neuroradiologie)
- Marc Sanson
(Université Pierre et Marie Curie Paris 6, Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM), UMR 975
INSERM U975
CNRS, UMR 7225
AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie 2-Mazarin)
- Jean-Yves Delattre
(Université Pierre et Marie Curie Paris 6, Centre de Recherche de l’Institut de Cerveau et de la Moelle Epinière (CRICM), UMR 975
INSERM U975
CNRS, UMR 7225
AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie 2-Mazarin)
- Dominique Figarella-Branger
(Université de la Méditerranée, Aix-Marseille, Faculté de Médecine La Timone, CRO2, UMR 911
AP-HM, Hôpital de la Timone, Service d’Anatomie Pathologique et de Neuropathologie)
- Aurélien de Reyniès
(Programme Cartes d’Identité des Tumeurs (CIT), Ligue Nationale Contre Le Cancer)
- François Ducray
(Hospices Civils de Lyon, Hôpital Neurologique, Service de Neuro-Oncologie
Cancer Research Centre of Lyon, INSERM U1052, CNRS UMR5286
Université Claude Bernard Lyon 1)
Abstract
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.
Suggested Citation
Aurélie Kamoun & Ahmed Idbaih & Caroline Dehais & Nabila Elarouci & Catherine Carpentier & Eric Letouzé & Carole Colin & Karima Mokhtari & Anne Jouvet & Emmanuelle Uro-Coste & Nadine Martin-Duverneuil, 2016.
"Integrated multi-omics analysis of oligodendroglial tumours identifies three subgroups of 1p/19q co-deleted gliomas,"
Nature Communications, Nature, vol. 7(1), pages 1-11, September.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms11263
DOI: 10.1038/ncomms11263
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