Bodineau, ClémentTomé, MercedesMurdoch, Piedad Del SocorroDurán, Raúl V2023-05-032023-05-032022-04-26http://hdl.handle.net/10668/19690Cancer cells metabolize glutamine mostly through glutaminolysis, a metabolic pathway that activates MTORC1. The AMPK-MTORC1 signaling axis is a key regulator of cell growth and proliferation. Our recent investigation identified that the connection between glutamine and AMPK is not restricted to glutaminolysis. Rather, we demonstrated the crucial role of ASNS (asparagine synthetase (glutamine-hydrolyzing)) and the GABA shunt for the metabolic control of the AMPK-MTORC1 axis during glutamine sufficiency. Our results elucidated a metabolic network by which glutamine metabolism regulates the MTORC1-macroautophagy/autophagy pathway through two independent branches involving glutaminolysis and ASNS-GABA shunt.Abbreviations: αKG: alpha-ketoglutarate; AMPK: AMP-activated protein kinase; ASNS: asparagine synthetase (glutamine-hydrolyzing); GLUD/GDH: glutamate dehydrogenase; GLS: glutaminase; GOT1: glutamic-oxaloacetic transaminase 1; MTORC1: mechanistic target of rapamycin kinase complex 1; TCA: tricarboxylic acid.enAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/ASNSGABA-shuntMTORC1glutamineglutamoptosisGlutamineAutophagyAMP-Activated Protein KinasesMechanistic Target of Rapamycin Complex 1gamma-Aminobutyric Acidresearch article35470752open access10.1080/15548627.2022.20628751554-8635PMC9629096https://doi.org/10.1080/15548627.2022.2062875https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629096/pdf