| Literature DB >> 34661146 |
P Leif Bergsagel1, W Michael Kuehl2.
Abstract
A comprehensive genomic analysis of structural variants in multiple myeloma in this issue highlights the key role of these events, involving primarily the immunoglobulin heavy chain locus in disease initiation and the MYC locus in disease progression. However, the current study reveals the large number of genomic hotspots, oncogenes, tumor suppressor genes, and recombination mechanisms that contribute to multiple myeloma heterogeneity. See related article by Rustad et al., p. 258. ©2020 American Association for Cancer Research.Entities:
Year: 2020 PMID: 34661146 PMCID: PMC8504774 DOI: 10.1158/2643-3230.BCD-20-0170
Source DB: PubMed Journal: Blood Cancer Discov ISSN: 2643-3230