| Literature DB >> 26366710 |
Ana Ortega-Molina1, Isaac W Boss2,3, Andres Canela4, Heng Pan5, Yanwen Jiang2,5, Chunying Zhao1, Man Jiang1, Deqing Hu6, Xabier Agirre2,7, Itamar Niesvizky2,3, Ji-Eun Lee8, Hua-Tang Chen4, Daisuke Ennishi9, David W Scott9, Anja Mottok9, Christoffer Hother9, Shichong Liu10, Xing-Jun Cao10, Wayne Tam11, Rita Shaknovich2, Benjamin A Garcia10, Randy D Gascoyne9, Kai Ge8, Ali Shilatifard6, Olivier Elemento5, Andre Nussenzweig4, Ari M Melnick2,3, Hans-Guido Wendel1.
Abstract
The gene encoding the lysine-specific histone methyltransferase KMT2D has emerged as one of the most frequently mutated genes in follicular lymphoma and diffuse large B cell lymphoma; however, the biological consequences of KMT2D mutations on lymphoma development are not known. Here we show that KMT2D functions as a bona fide tumor suppressor and that its genetic ablation in B cells promotes lymphoma development in mice. KMT2D deficiency also delays germinal center involution and impedes B cell differentiation and class switch recombination. Integrative genomic analyses indicate that KMT2D affects methylation of lysine 4 on histone H3 (H3K4) and expression of a set of genes, including those in the CD40, JAK-STAT, Toll-like receptor and B cell receptor signaling pathways. Notably, other KMT2D target genes include frequently mutated tumor suppressor genes such as TNFAIP3, SOCS3 and TNFRSF14. Therefore, KMT2D mutations may promote malignant outgrowth by perturbing the expression of tumor suppressor genes that control B cell-activating pathways.Entities:
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Year: 2015 PMID: 26366710 PMCID: PMC4676270 DOI: 10.1038/nm.3943
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440