Abstract
In this issue of Blood, Gallipoli et al report that by performing an elegant clustered regularly interspaced short palindromic repeats (CRISPR) screen of FLT3 internal tandem duplication–positive (FLT3-ITD1) acute myeloid leukemia (AML) cells, they have identified that FLT3 inhibition exposes a therapeutically relevant metabolic dependency on glutaminolysis.
Original language | English (US) |
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Pages (from-to) | 1631-1632 |
Number of pages | 2 |
Journal | Blood |
Volume | 131 |
Issue number | 15 |
DOIs | |
State | Published - Apr 12 2018 |
ASJC Scopus subject areas
- Biochemistry
- Immunology
- Hematology
- Cell Biology