An RCOR1 loss–associated gene expression signature identifies a prognostically significant DLBCL subgroup

Author:

Chan Fong Chun12ORCID,Telenius Adele1,Healy Shannon1,Ben-Neriah Susana1,Mottok Anja1,Lim Raymond1ORCID,Drake Marie1,Hu Sandy1,Ding Jiarui3ORCID,Ha Gavin23,Scott David W.1,Kridel Robert1,Bashashati Ali3,Rogic Sanja1,Johnson Nathalie4,Morin Ryan D.56ORCID,Rimsza Lisa M.7,Sehn Laurie1,Connors Joseph M.1ORCID,Marra Marco A.58,Gascoyne Randy D.1,Shah Sohrab P.3,Steidl Christian1

Affiliation:

1. Center for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, BC, Canada;

2. Bioinformatics Graduate Program, University of British Columbia, Vancouver, BC, Canada;

3. Department of Molecular Oncology, British Columbia Cancer Agency, Vancouver, BC, Canada;

4. Department of Oncology, McGill University, Montreal, QC, Canada;

5. Genome Sciences Center, British Columbia Cancer Agency, Vancouver, BC, Canada;

6. Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, BC, Canada;

7. Department of Pathology, University of Arizona, Tucson, AZ; and

8. Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada

Abstract

Key Points Integration of genome-wide copy number and whole transcriptome data identifies key mutational events in the pathogenesis of DLBCL. Genomic deletions in RCOR1 are associated with a specific gene expression signature and with unfavorable clinical outcomes in DLBCL patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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