| Literature DB >> 30282799 |
Rabea Wagener1,2, Cristina López1,2, Kortine Kleinheinz3,4, Julia Bausinger1, Sietse M Aukema2, Inga Nagel2,5, Umut H Toprak3,6,7, Julian Seufert3,6,7, Janine Altmüller8, Holger Thiele9, Christof Schneider10, Julia Kolarova1,2, Jeongbin Park3,7, Daniel Hübschmann3,4,11, Eva M Murga Penas2, Hans G Drexler12, Andishe Attarbaschi13, Randi Hovland14, Eigil Kjeldsen15, Michael Kneba16, Udo Kontny17, Laurence de Leval18, Peter Nürnberg8, Ilske Oschlies19, David Oscier20, Brigitte Schlegelberger21, Stephan Stilgenbauer10, Wilhelm Wössmann22, Matthias Schlesner6, Birgit Burkhardt23, Wolfram Klapper19, Elaine S Jaffe24, Ralf Küppers25, Reiner Siebert1,2.
Abstract
The WHO Classification of Tumours of Haematopoietic and Lymphoid Tissue notes instances of Burkitt lymphoma/leukemia (BL) with IG-MYC rearrangement displaying a B-cell precursor immunophenotype (termed herein "preBLL"). To characterize the molecular pathogenesis of preBLL, we investigated 13 preBLL cases (including 1 cell line), of which 12 were analyzable using genome, exome, and targeted sequencing, imbalance mapping, and DNA methylation profiling. In 5 patients with reads across the IG-MYC breakpoint junctions, we found evidence that the translocation derived from an aberrant VDJ recombination, as is typical for IG translocations arising in B-cell precursors. Genomic changes like biallelic IGH translocations or VDJ rearrangements combined with translocation into the VDJ region on the second allele, potentially preventing expression of a productive immunoglobulin, were detected in 6 of 13 cases. We did not detect mutations in genes frequently altered in BL, but instead found activating NRAS and/or KRAS mutations in 7 of 12 preBLLs. Gains on 1q, recurrent in BL and preB lymphoblastic leukemia/lymphoma (pB-ALL/LBL), were detected in 7 of 12 preBLLs. DNA methylation profiling showed preBLL to cluster with precursor B cells and pB-ALL/LBL, but apart from BL. We conclude that preBLL genetically and epigenetically resembles pB-ALL/LBL rather than BL. Therefore, we propose that preBLL be considered as a pB-ALL/LBL with recurrent genetic abnormalities.Entities:
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Year: 2018 PMID: 30282799 PMCID: PMC6251006 DOI: 10.1182/blood-2018-03-842088
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113