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.
Original language | English (US) |
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Pages (from-to) | 221-223 |
Number of pages | 3 |
Journal | Blood cancer discovery |
Volume | 1 |
Issue number | 3 |
DOIs | |
State | Published - Nov 1 2020 |
ASJC Scopus subject areas
- General Medicine