| Literature DB >> 29533464 |
Abdullah Alholle1, Marie Karanian2,3, Anna T Brini4, Mark R Morris5, Vinodh Kannappan5, Stefania Niada4, Angela Niblett6, Dominique Ranchère-Vince2, Daniel Pissaloux2,3, Christophe Delfour7, Aurelie Maran-Gonzalez8, Cristina R Antonescu9, Vaiyapuri Sumathi6, Franck Tirode3,10, Farida Latif1.
Abstract
In recent years, undifferentiated small round cell sarcomas (USRCSs) have been divided into a variety of new, rare, sarcoma subtypes, including the group of Ewing-like sarcomas, which have the morphological appearance of Ewing sarcomas, but carry CIC-DUX4, BCOR-CCNB3 and other gene fusions different from the classic EWSR1-ETS gene fusion. Using high-throughput RNA-sequencing (RNA-seq) analyses, we identified a novel recurrent gene fusion, CRTC1-SS18, in two cases of USRCS that lacked any known translocation. RNA-seq results were confirmed by reverse transcription polymerase chain reaction, long-range polymerase chain reaction, and fluorescence in situ hybridization. In vitro, we showed that the cells expressing the gene fusion were morphologically distinct and had enhanced oncogenic potential as compared with control cells. Expression profile comparisons with tumours of other sarcoma subtypes demonstrated that both cases clustered close to EWSR1-CREB1-positive tumours. Moreover, these analyses indicated enhanced NTRK1 expression in CRTC1-SS18-positive tumours. We conclude that the novel gene fusion identified in this study adds a new subtype to the USRCSs with unique gene signatures, and may be of therapeutic relevance.Entities:
Keywords: Ewing sarcoma; RNA-seq; gene fusion; undifferentiated small round cell sarcoma
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Year: 2018 PMID: 29533464 PMCID: PMC7988498 DOI: 10.1002/path.5071
Source DB: PubMed Journal: J Pathol ISSN: 0022-3417 Impact factor: 7.996