α-Ketoglutarate dehydrogenase is a therapeutic vulnerability in acute myeloid leukemia

Perturbations in intermediary metabolism contribute to the pathogenesis of acute myeloid leukemia (AML) and can produce therapeutically actionable dependencies. Here, we probed whether α-ketoglutarate (αKG) metabolism represents a specific vulnerability in AML. Using functional genomics, metabolomics, and mouse models, we identified the αKG dehydrogenase complex, which catalyzes the conversion of αKG to succinyl coenzyme A, as a molecular dependency across multiple models of adverse-risk AML. Inhibition of 2-oxoglutarate dehydrogenase (OGDH), the E1 subunit of the αKG dehydrogenase complex, impaired AML progression and drove differentiation. Mechanistically, hindrance of αKG flux through the tricarboxylic acid (TCA) cycle resulted in rapid exhaustion of aspartate pools and blockade of de novo nucleotide biosynthesis, whereas cellular bioenergetics was largely preserved. Additionally, increased αKG levels after OGDH inhibition affected the biosynthesis of other critical amino acids. Thus, this work has identified a previously undescribed, functional link between certain TCA cycle components and nucleotide biosynthesis enzymes across AML. This metabolic node may serve as a cancer-specific vulnerability, amenable to therapeutic targeting in AML and perhaps in other cancers with similar metabolic wiring.

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Publication Details

Journal
Blood
Published
2025-01-10
DOI
https://doi.org/10.1182/blood.2024025245
Citations
13
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
23.01
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article

α-Ketoglutarate dehydrogenase is a therapeutic vulnerability in acute myeloid leukemia

Zohar Sachs, Timour Baslan, Justin R. Cross, Lydia W.S. Finley et al.
13 citations
Blood
Acute Myeloid Leukemia Research
23.01
article

α-Ketoglutarate dehydrogenase is a therapeutic vulnerability in acute myeloid leukemia

Zohar Sachs, Timour Baslan, Justin R. Cross, Lydia W.S. Finley, Jossie J. Yashinskie, Scott W. Lowe, Almudena Chaves Perez, Sha Tian, Sudha Janaki‐Raman, Valentin J.A. Barthet, Benjamin T. Jackson, Riccardo Mezzadra, Yu-Jui Ho, Scott E. Millman, Chi-Chao Chen, Michelle Saoi, John P. Morris, Varun Narendra, Tom Devine
article en
13 citations

Abstract

Perturbations in intermediary metabolism contribute to the pathogenesis of acute myeloid leukemia (AML) and can produce therapeutically actionable dependencies. Here, we probed whether α-ketoglutarate (αKG) metabolism represents a specific vulnerability in AML. Using functional genomics, metabolomics, and mouse models, we identified the αKG dehydrogenase complex, which catalyzes the conversion of αKG to succinyl coenzyme A, as a molecular dependency across multiple models of adverse-risk AML. Inhibition of 2-oxoglutarate dehydrogenase (OGDH), the E1 subunit of the αKG dehydrogenase complex, impaired AML progression and drove differentiation. Mechanistically, hindrance of αKG flux through the tricarboxylic acid (TCA) cycle resulted in rapid exhaustion of aspartate pools and blockade of de novo nucleotide biosynthesis, whereas cellular bioenergetics was largely preserved. Additionally, increased αKG levels after OGDH inhibition affected the biosynthesis of other critical amino acids. Thus, this work has identified a previously undescribed, functional link between certain TCA cycle components and nucleotide biosynthesis enzymes across AML. This metabolic node may serve as a cancer-specific vulnerability, amenable to therapeutic targeting in AML and perhaps in other cancers with similar metabolic wiring.

BloodVol. 145(13)
Memorial Sloan Kettering Cancer Center (US), Howard Hughes Medical Institute (US), Cornell University (US), University of Minnesota System (US), University of Minnesota Medical Center (US)
Good health and well-being
Openalex Percentile: Top 0%
Acute Myeloid Leukemia Research
23.01
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