Taming the Heterogeneity of Aggressive Lymphomas for Precision Therapy

Author:

Young Ryan M.1,Phelan James D.1,Shaffer Arthur L.1,Wright George W.2,Huang Da Wei1,Schmitz Roland1,Johnson Calvin3,Oellerich Thomas1,Wilson Wyndham1,Staudt Louis M.1

Affiliation:

1. Lymphoid Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA;

2. Biometric Research Branch, Division of Cancer Diagnosis and Treatment, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA

3. Office of Intramural Research, Center for Information Technology, National Institutes of Health, Bethesda, Maryland 20892, USA

Abstract

Genomic analyses of diffuse large B cell lymphoma (DLBCL) are revealing the genetic and phenotypic heterogeneity of these aggressive lymphomas. In part, this heterogeneity reflects the existence of distinct genetic subtypes that acquire characteristic constellations of somatic genetic alterations to converge on the DLBCL phenotype. In parallel, functional genomic screens and proteomic analyses have identified multiprotein assemblies that coordinate oncogenic survival signaling in DLBCL. In this review, we merge these recent insights into a unified conceptual framework with implications for the design of precision medicine trials in DLBCL.

Publisher

Annual Reviews

Subject

Cancer Research,Cell Biology,Oncology

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