肉瘤
生物
转录组
融合基因
癌症研究
基因
同种类的
细胞
计算生物学
病理
基因表达
医学
遗传学
物理
热力学
作者
Sarah Watson,Virginie Perrin,Delphine Guillemot,Stéphanie Reynaud,Jean‐Michel Coindre,Marie Karanian,Jean‐Marc Guinebretière,Paul Fréneaux,François Le Loarer,Mégane Bouvet,Louise Galmiche,Frédérique Larousserie,Élisabeth Longchampt,Dominique Ranchere‐Vince,Gaëlle Pierron,Olivier Delattre,Franck Tirode
摘要
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. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
科研通智能强力驱动
Strongly Powered by AbleSci AI