Diverse mutations and structural variations contribute to Notch
signaling deregulation in paediatric T-cell lymphoblastic lymphoma
Abstract
Background T-cell lymphoblastic lymphoma (T-LBL) is an aggressive
neoplasm closely related to T-cell acute lymphoblastic leukaemia
(T-ALL). Despite their similarities, and contrary to T-ALL, studies on
pediatric T-LBL are scarce and, therefore, its molecular landscape has
not been fully elucidated yet. Procedure To characterize the genetic and
molecular heterogeneity of paediatric T-LBL, 33 patients were analyzed
using an integrated approach, including targeted next generation
sequencing, RNA-sequencing transcriptome analysis and copy-number
arrays. Results Copy number and mutational analyses allowed the
detection of recurrent homozygous deletions of 9p/CDKN2A (78%), trisomy
20 (19%) and gains of 17q24-q25 (16%), as well as frequent mutations
of NOTCH1 (62%), followed by BCL11B (23%), WT1 (19%) and FBXW7, PHF6
and RPL10 genes (15%, respectively). This genetic profile did not
differ to that described in T-ALL in terms of mutation incidence and
global genomic complexity level but unveiled virtually exclusive 17q25
gains and trisomy 20 in T-LBL. Additionally, we identified novel gene
fusions in paediatric T-LBL including NOTCH1-IKZF2, RNGTT-SNAP91 and
DDX3X-MLLT10, the latter being the only one previously described in
T-ALL. Moreover, clinical correlations highlighted the presence of Notch
pathway alterations as a factor related to favorable outcome.
Conclusions In summary, the genomic landscape of paediatric T-LBL is
similar to that observed in T-ALL and Notch signaling pathway
deregulation remains the cornerstone in its pathogenesis, including not
only mutations but fusion genes targeting NOTCH1.