Ontology highlight
ABSTRACT: Purpose
Acute myeloid leukemia (AML) is a hematologic malignancy characterized by the accumulation of immature myeloid precursor cells. AML is poorly responsive to conventional chemotherapy and a diagnosis of AML is usually fatal. More effective and less toxic forms of therapy are desperately needed. AML cells are known to be highly dependent on the amino acid glutamine for their survival. These studies were directed at determining the effects of glutaminase inhibition on metabolism in AML and identifying general weaknesses that can be exploited therapeutically.Experimental design
AML cancer cell lines, primary AML cells, and mouse models of AML and acute lymphoblastic leukemia (ALL) were utilized.Results
We show that blocking glutamine metabolism through the use of
SUBMITTER: Gregory MA
PROVIDER: S-EPMC6642698 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature