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Fusion transcripts FYN-TRAF3IP2 and KHDRBS1-LCK hijack T cell receptor signaling in peripheral T-cell lymphoma, not otherwise specified

Authors :
Daan Dierickx
Philippe Gaulard
Carlos Graux
Koen Debackere
Laurence de Leval
Nicole Mentens
Jan Cools
Lucienne Michaux
Kris Jacobs
Thomas Tousseyn
Sofie Demeyer
Olga Gielen
Michaël Broux
Iwona Wlodarska
Marlies Vanden Bempt
Lukas Marcelis
Gregor Verhoef
UCL - SSS/IREC/MONT - Pôle Mont Godinne
UCL - (MGD) Service d'hématologie
Source :
Nature communications, vol. 12, no. 1, pp. 3705, Nature communications, Vol. 12, no.1, p. 3705 (2021), Nature Communications, Vol 12, Iss 1, Pp 1-19 (2021), Nature Communications
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

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.<br />Peripheral T cell lymphoma (PTCL) not otherwise specified (NOS) is a subgroup of PTCL, which has no distinctive features and is poorly characterized at the genetic level. Here, the authors identify two fusion transcripts that activate T cell receptor complex signalling and confer therapeutic vulnerability in PTCL-NOS.

Subjects

Subjects :
0301 basic medicine
Oncogene Proteins, Fusion
General Physics and Astronomy
Kaplan-Meier Estimate
Proto-Oncogene Proteins c-fyn
Cohort Studies
Mice
0302 clinical medicine
RNA-Seq
Receptor
Cancer genetics
Multidisciplinary
Forkhead Box Protein O1
Intracellular Signaling Peptides and Proteins
NF-kappa B
RNA-Binding Proteins
hemic and immune systems
DNA-Binding Proteins
Gene Expression Regulation, Neoplastic
Sin3 Histone Deacetylase and Corepressor Complex
medicine.anatomical_structure
030220 oncology & carcinogenesis
T-cell lymphoma
Adaptor Proteins, Signal Transducing/genetics
Adaptor Proteins, Signal Transducing/metabolism
Animals
Cell Line, Tumor
Cell Membrane/metabolism
DNA-Binding Proteins/genetics
DNA-Binding Proteins/metabolism
Forkhead Box Protein O1/genetics
Forkhead Box Protein O1/metabolism
Gene Expression Regulation, Neoplastic/genetics
Humans
Intracellular Signaling Peptides and Proteins/metabolism
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)/genetics
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)/metabolism
Lymphoma, T-Cell, Peripheral/genetics
Lymphoma, T-Cell, Peripheral/metabolism
Lymphoma, T-Cell, Peripheral/pathology
Mice, Inbred C57BL
NF-kappa B/metabolism
Oncogene Proteins, Fusion/genetics
Oncogene Proteins, Fusion/metabolism
Proto-Oncogene Proteins c-fyn/genetics
Proto-Oncogene Proteins c-fyn/metabolism
RNA-Binding Proteins/genetics
RNA-Binding Proteins/metabolism
Receptors, Antigen, T-Cell/metabolism
Signal Transduction/genetics
Sin3 Histone Deacetylase and Corepressor Complex/genetics
Sin3 Histone Deacetylase and Corepressor Complex/metabolism
bcl-X Protein/antagonists & inhibitors
bcl-X Protein/metabolism
Signal transduction
Signal Transduction
Science
T cell
Receptors, Antigen, T-Cell
bcl-X Protein
Peripheral T-cell lymphoma not otherwise specified
Biology
Article
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
FYN
medicine
Adaptor Proteins, Signal Transducing
Cell Membrane
T-cell receptor
Lymphoma, T-Cell, Peripheral
General Chemistry
medicine.disease
Lymphoma
030104 developmental biology
Lymphocyte Specific Protein Tyrosine Kinase p56(lck)
Cancer research
Ex vivo

Details

ISSN :
20411723
Volume :
12
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....133ce4ef8eab96b32fc1be9ac3896731
Full Text :
https://doi.org/10.1038/s41467-021-24037-4