Transcriptomic definition of molecular subgroups of small round cell sarcomas

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Watson, Sarah | Perrin, Virginie | Guillemot, Delphine | Reynaud, Stéphanie | Coindre, Jean-Michel | Karanian, Marie | Guinebretière, Jean-Marc | Fréneaux, Paul | Le Loarer, Francois | Bouvet, Megane | Galmiche-Rolland, Louise | Larousserie, Frédérique | Longchampt, Elisabeth | Ranchère-Vince, Dominique | Pierron, Gaëlle | Delattre, Olivier | Tirode, Franck

Edité par CCSD ; John Wiley & Sons -

International audience. Sarcoma represents a highly heterogeneous group of tumours. We report here the first unbiased and systematic search for gene fusions combined with unsupervised expression analysis of a series of 184 small round cell sarcomas. Fusion genes were detected in 59% of samples, with half of them being observed recurrently. We identified biologically homogeneous groups of tumours such as the CIC-fused (to DUX4, FOXO4 or NUTM1) and BCOR-rearranged (BCOR-CCNB3, BCOR-MAML3, ZC3H7B-BCOR, and BCOR internal duplication) tumour groups. VGLL2-fused tumours represented a more biologically and pathologically heterogeneous group. This study also refined the characteristics of some entities such as EWSR1-PATZ1 spindle cell sarcoma or FUS-NFATC2 bone tumours that are different from EWSR1-NFATC2 tumours and transcriptionally resemble CIC-fused tumour entities. We also describe a completely novel group of epithelioid and spindle-cell rhabdomyosarcomas characterized by EWSR1- or FUS-TFCP2 fusions. Finally, expression data identified some potentially new therapeutic targets or pathways.

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