FYN公司
外周T细胞淋巴瘤
淋巴瘤
T细胞
癌症研究
体内
生物
T细胞淋巴瘤
T细胞受体
医学
信号转导
细胞生物学
遗传学
免疫学
酪氨酸激酶
免疫系统
作者
Koen Debackere,Lukas Marcelis,Sofie Demeyer,Marlies Vanden Bempt,Nele Mentens,Olga Gielen,Kris Jacobs,Michael Broüx,Gregor Verhoef,Lucienne Michaux,Carlos Graux,Iwona Włodarska,Philippe Gaulard,Laurence de Leval,Thomas Tousseyn,Jan Cools,Daan Dierickx
标识
DOI:10.1038/s41467-021-24037-4
摘要
Peripheral T-cell lymphoma (PTCL) is a heterogeneous group of non-Hodgkin lymphomas with poor prognosis. Up to 30% of PTCL lack distinctive features and are classified as PTCL, not otherwise specified (PTCL-NOS). To further improve our understanding of the genetic landscape and biology of PTCL-NOS, we perform RNA-sequencing of 18 cases and validate results in an independent cohort of 37 PTCL cases. We identify FYN-TRAF3IP2, KHDRBS1-LCK and SIN3A-FOXO1 as new in-frame fusion transcripts, with FYN-TRAF3IP2 as a recurrent fusion detected in 8 of 55 cases. Using ex vivo and in vivo experiments, we demonstrate that FYN-TRAF3IP2 and KHDRBS1-LCK activate signaling pathways downstream of the T cell receptor (TCR) complex and confer therapeutic vulnerability to clinically available drugs.
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