Menin and Menin-Associated Proteins Coregulate Cancer Energy Metabolism.
Ontology highlight
ABSTRACT: The interplay between glycolysis and mitochondrial oxidative phosphorylation (OXPHOS) is central to maintain energy homeostasis. It remains to be determined whether there is a mechanism governing metabolic fluxes based on substrate availability in microenvironments. Here we show that menin is a key transcription factor regulating the expression of OXPHOS and glycolytic genes in cancer cells and primary tumors with poor prognosis. A group of menin-associated proteins (MAPs), including KMT2A, MED12, WAPL, and GATA3, is found to restrain menin's full function in this transcription regulation. shRNA knockdowns of menin and MAPs result in reduced ATP production with proportional alterations of cellular energy generated through glycolysis and OXPHOS. When shRNA knockdown cells are exposed to met
SUBMITTER: Chou CW
PROVIDER: S-EPMC7564175 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature
ACCESS DATA