| Literature DB >> 34365473 |
Frits van Rhee1, Brian A Walker2, Eileen M Boyle3, Adam Rosenthal4, Hussein Ghamlouch3, Yan Wang1,5, Phillip Farmer1,5, Michael Rutherford5, Cody Ashby5, Michael Bauer5, Sarah K Johnson1, Christopher P Wardell5, Yubao Wang3, Antje Hoering4, Carolina Schinke1, Sharmilan Thanendrarajan1, Maurizio Zangari1, Bart Barlogie6, Madhav V Dhodapkar7, Faith E Davies3, Gareth J Morgan3.
Abstract
Sequencing studies have shed some light on the pathogenesis of progression from smouldering multiple myeloma (SMM) and symptomatic multiple myeloma (MM). Given the scarcity of smouldering samples, little data are available to determine which translational programmes are dysregulated and whether the mechanisms of progression are uniform across the main molecular subgroups. In this work, we investigated 223 SMM and 1348 MM samples from the University of Arkansas for Medical Sciences (UAMS) for which we had gene expression profiling (GEP). Patients were analysed by TC-7 subgroup for gene expression changes between SMM and MM. Among the commonly dysregulated genes in each subgroup, PHF19 and EZH2 highlight the importance of the PRC2.1 complex. We show that subgroup specific differences exist even at the SMM stage of disease with different biological features driving progression within each TC molecular subgroup. These data suggest that MMSET SMM has already transformed, but that the other precursor diseases are distinct clinical entities from their symptomatic counterpart.Entities:
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Year: 2021 PMID: 34365473 DOI: 10.1038/s41375-021-01379-y
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528