TY - JOUR
T1 - Integrated multi-omics analysis of oligodendroglial tumours identifies three subgroups of 1p/19q co-deleted gliomas
AU - Pola Network
AU - Kamoun, Aurélie
AU - Idbaih, Ahmed
AU - Dehais, Caroline
AU - Elarouci, Nabila
AU - Carpentier, Catherine
AU - Letouzé, Eric
AU - Colin, Carole
AU - Mokhtari, Karima
AU - Jouvet, Anne
AU - Uro-Coste, Emmanuelle
AU - Martin-Duverneuil, Nadine
AU - Sanson, Marc
AU - Delattre, Jean Yves
AU - Figarella-Branger, Dominique
AU - De Reyniès, Aurélien
AU - Ducray, François
AU - Adam, Clovis
AU - Andraud, Marie
AU - Aubriot-Lorton, Marie Hélène
AU - Bauchet, Luc
AU - Beauchesne, Patrick
AU - Bielle, Franck
AU - Blechet, Claire
AU - Campone, Mario
AU - Carpentier, Antoine F.
AU - Carpiuc, Ioana
AU - Cazals-Hatem, Dominique
AU - Chenard, Marie Pierre
AU - Chiforeanu, Danchristian
AU - Chinot, Olivier
AU - Cohen-Moyal, Elisabeth
AU - Colin, Philippe
AU - Dam-Hieu, Phong
AU - Desenclos, Christine
AU - Desse, Nicolas
AU - Dhermain, Frederic
AU - Diebold, Marie Danièle
AU - Eimer, Sandrine
AU - Faillot, Thierry
AU - Fesneau, Mélanie
AU - Fontaine, Denys
AU - Gaillard, Stéphane
AU - Gauchotte, Guillaume
AU - Gaultier, Claude
AU - Ghiringhelli, François
AU - Godard, Joel
AU - Gueye, Edouard Marcel
AU - Guillamo, Jean Sebastien
AU - Hamdi-Elouadhani, Selma
AU - Honnorat, Jerome
PY - 2016/4/19
Y1 - 2016/4/19
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84973326510&partnerID=8YFLogxK
U2 - 10.1038/ncomms11263
DO - 10.1038/ncomms11263
M3 - Article
C2 - 27090007
AN - SCOPUS:84973326510
SN - 2041-1723
VL - 7
JO - Nature Communications
JF - Nature Communications
M1 - 11263
ER -