Abstract
Although CEBPA mutations are among the most common genetic abnormalities in acute myeloid leukemia (AML), the transformation mechanism remains largely obscure. In this issue of Cancer Cell, Zhang and colleagues report that SOX4 is a direct target and crucial mediator of C/EBPα mutants in AML, revealing a potential therapeutic avenue.
Original language | English |
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Article number | N/A |
Pages (from-to) | 557-559 |
Number of pages | 3 |
Journal | CANCER CELL |
Volume | 24 |
Issue number | 5 |
DOIs | |
Publication status | Published - Nov 2013 |