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The genomic and transcriptional landscape of primary central nervous system lymphoma.

Josefine RadkeNaveed IshaqueRandi KollZuguang GuElisa SchumannLina SieverlingSebastian UhrigDaniel HübschmannUmut H ToprakCristina LópezXavier Pastor HostenchSimone BorgoniDilafruz JuraevaFabienne PritschNagarajan ParamasivamGnana Prakash BalasubramanianMatthias SchlesnerShashwat SahayMarc WenigerDebora PehlHelena RadbruchAnja OsterlohAgnieszka KorfelMartin MischJulia OnkenKatharina FaustPeter VajkoczyDag MoskoppYawen WangAndreas JödickeLorenz TrümperIoannis AnagnostopoulosDido LenzeRalf KüppersMichael HummelClemens A SchmittOtmar D WiestlerStephan WolfAndreas UnterbergRoland EilsChristel Herold-MendeBenedikt Brorsnull nullReiner SiebertStefan WiemannFrank L Heppner
Published in: Nature communications (2022)
Primary lymphomas of the central nervous system (PCNSL) are mainly diffuse large B-cell lymphomas (DLBCLs) confined to the central nervous system (CNS). Molecular drivers of PCNSL have not been fully elucidated. Here, we profile and compare the whole-genome and transcriptome landscape of 51 CNS lymphomas (CNSL) to 39 follicular lymphoma and 36 DLBCL cases outside the CNS. We find recurrent mutations in JAK-STAT, NFkB, and B-cell receptor signaling pathways, including hallmark mutations in MYD88 L265P (67%) and CD79B (63%), and CDKN2A deletions (83%). PCNSLs exhibit significantly more focal deletions of HLA-D (6p21) locus as a potential mechanism of immune evasion. Mutational signatures correlating with DNA replication and mitosis are significantly enriched in PCNSL. TERT gene expression is significantly higher in PCNSL compared to activated B-cell (ABC)-DLBCL. Transcriptome analysis clearly distinguishes PCNSL and systemic DLBCL into distinct molecular subtypes. Epstein-Barr virus (EBV)+ CNSL cases lack recurrent mutational hotspots apart from IG and HLA-DRB loci. We show that PCNSL can be clearly distinguished from DLBCL, having distinct expression profiles, IG expression and translocation patterns, as well as specific combinations of genetic alterations.
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