| First Author | Chen WL | Year | 2016 |
| Journal | Cancer Cell | Volume | 30 |
| Issue | 5 | Pages | 779-791 |
| PubMed ID | 27746145 | Mgi Jnum | J:238014 |
| Mgi Id | MGI:5817856 | Doi | 10.1016/j.ccell.2016.09.006 |
| Citation | Chen WL, et al. (2016) Enhanced Fructose Utilization Mediated by SLC2A5 Is a Unique Metabolic Feature of Acute Myeloid Leukemia with Therapeutic Potential. Cancer Cell 30(5):779-791 |
| abstractText | Rapidly proliferating leukemic progenitor cells consume substantial glucose, which may lead to glucose insufficiency in bone marrow. We show that acute myeloid leukemia (AML) cells are prone to fructose utilization with an upregulated fructose transporter GLUT5, which compensates for glucose deficiency. Notably, AML patients with upregulated transcription of the GLUT5-encoding gene SLC2A5 or increased fructose utilization have poor outcomes. Pharmacological blockage of fructose uptake ameliorates leukemic phenotypes and potentiates the cytotoxicity of the antileukemic agent, Ara-C. In conclusion, this study highlights enhanced fructose utilization as a metabolic feature of AML and a potential therapeutic target. |
