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Coordinative Metabolism of Glutamine Carbon and Nitrogen in Proliferating Cancer Cells Under Hypoxia

Overview
Journal Nat Commun
Specialty Biology
Date 2019 Jan 16
PMID 30643150
Citations 106
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Abstract

Under hypoxia, most of glucose is converted to secretory lactate, which leads to the overuse of glutamine-carbon. However, under such a condition how glutamine nitrogen is disposed to avoid over-accumulating ammonia remains to be determined. Here we identify a metabolic flux of glutamine to secretory dihydroorotate, which is indispensable to glutamine-carbon metabolism under hypoxia. We found that glutamine nitrogen is necessary to nucleotide biosynthesis, but enriched in dihyroorotate and orotate rather than processing to its downstream uridine monophosphate under hypoxia. Dihyroorotate, not orotate, is then secreted out of cells. Furthermore, we found that the specific metabolic pathway occurs in vivo and is required for tumor growth. The identified metabolic pathway renders glutamine mainly to acetyl coenzyme A for lipogenesis, with the rest carbon and nitrogen being safely removed. Therefore, our results reveal how glutamine carbon and nitrogen are coordinatively metabolized under hypoxia, and provide a comprehensive understanding on glutamine metabolism.

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References
1.
Adeva M, Souto G, Blanco N, Donapetry C . Ammonium metabolism in humans. Metabolism. 2012; 61(11):1495-511. DOI: 10.1016/j.metabol.2012.07.007. View

2.
Yang C, Sudderth J, Dang T, Bachoo R, Bachoo R, McDonald J . Glioblastoma cells require glutamate dehydrogenase to survive impairments of glucose metabolism or Akt signaling. Cancer Res. 2009; 69(20):7986-93. PMC: 2764330. DOI: 10.1158/0008-5472.CAN-09-2266. View

3.
Kappler M, Pabst U, Rot S, Taubert H, Wichmann H, Schubert J . Normoxic accumulation of HIF1α is associated with glutaminolysis. Clin Oral Investig. 2016; 21(1):211-224. DOI: 10.1007/s00784-016-1780-9. View

4.
DeBerardinis R, Mancuso A, Daikhin E, Nissim I, Yudkoff M, Wehrli S . Beyond aerobic glycolysis: transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis. Proc Natl Acad Sci U S A. 2007; 104(49):19345-50. PMC: 2148292. DOI: 10.1073/pnas.0709747104. View

5.
Birsoy K, Wang T, Chen W, Freinkman E, Abu-Remaileh M, Sabatini D . An Essential Role of the Mitochondrial Electron Transport Chain in Cell Proliferation Is to Enable Aspartate Synthesis. Cell. 2015; 162(3):540-51. PMC: 4522279. DOI: 10.1016/j.cell.2015.07.016. View