Amelio Oncogene.pdf (909.35 kB)
p73 regulates serine biosynthesis in cancer.
journal contribution
posted on 2020-05-29, 10:26 authored by I Amelio, EK Markert, A Rufini, AV Antonov, BS Sayan, P Tucci, M Agostini, TC Mineo, AJ Levine, G MelinoActivation of serine biosynthesis supports growth and proliferation of cancer cells. Human cancers often exhibit overexpression of phosphoglycerate dehydrogenase (PHGDH), the metabolic enzyme that catalyses the reaction that diverts serine biosynthesis from the glycolytic pathway. By refueling serine biosynthetic pathways, cancer cells sustain their metabolic requirements, promoting macromolecule synthesis, anaplerotic flux and ATP. Serine biosynthesis intersects glutaminolysis and together with this pathway provides substrates for production of antioxidant GSH. In human lung adenocarcinomas we identified a correlation between serine biosynthetic pathway and p73 expression. Metabolic profiling of human cancer cell line revealed that TAp73 activates serine biosynthesis, resulting in increased intracellular levels of serine and glycine, associated to accumulation of glutamate, tricarboxylic acid (TCA) anaplerotic intermediates and GSH. However, at molecular level p73 does not directly regulate serine metabolic enzymes, but transcriptionally controls a key enzyme of glutaminolysis, glutaminase-2 (GLS-2). p73, through GLS-2, favors conversion of glutamine in glutamate, which in turn drives the serine biosynthetic pathway. Serine and glutamate can be then employed for GSH synthesis, thus the p73-dependent metabolic switch enables potential response against oxidative stress. In knockdown experiment, indeed, TAp73 depletion completely abrogates cancer cell proliferation capacity in serine/glycine-deprivation, supporting the role of p73 to help cancer cells under metabolic stress. These findings implicate p73 in regulation of cancer metabolism and suggest that TAp73 influences glutamine and serine metabolism, affecting GSH synthesis and determining cancer pathogenesis.
Funding
This work has been supported by the Medical Research Council, United Kingdom; MIUR, MinSan/IDI-IRCCS (RF73, RF57), ACC12, AIRC (2011-IG11955), AIRC 5xmille (MCO #9979) to GM Work was supported by Ministry of Education and Science of the Russian Federation (11.G34.31.0069) to GM & (14.B37.21.1967) to AAV.
History
Citation
Oncogene, 2014, 33 (42), pp. 5039-5046Author affiliation
/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/School of Medicine/Department of Cancer Studies and Molecular MedicineVersion
- AM (Accepted Manuscript)
Published in
OncogeneVolume
33Issue
42Pagination
5039-5046Publisher
Springer Natureeissn
1476-5594Acceptance date
2013-09-24Copyright date
2013Publisher DOI
Language
engAdministrator link
Publisher version
https://www.nature.com/articles/onc2013456Usage metrics
Categories
Keywords
Cell Line, TumorCell ProliferationDNA-Binding ProteinsGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticGlutaminaseHumansLung NeoplasmsNuclear ProteinsPhosphoglycerate DehydrogenasePhosphoric Monoester HydrolasesProtein IsoformsSerineTransaminasesTranscription, GeneticTumor Suppressor Proteins