eLifeCancer BiologyPeer-reviewed journal article
Mitochondrial ETF insufficiency drives neoplastic growth by selectively optimizing cancer bioenergetics
David J. PapadopoliiD, Ranveer PaliaiD, Predrag JovanoviciD, Sébastien TabarièsiD, Emma Ciccolini, Valérie SabouriniD, Sebastian IgelmanniD, Shannon McLaughlaniD, Lesley ZhaniD, HaEun KimiD, Nabila ChekkaliD, Krzysztof J. SzkopiD, Thierry BertomeuiD, Jibin Zeng, Julia Avian VassalakisiD, Farzaneh AfzaliiD, Slim MzoughiiD, Ernesto GuccioneiD, Mike TyersiD, Daina Zofija AvizonisiD, Ola Segnestam LarssoniD, Lynne-Marie M PostovitiD, Sergej DjuranovićiD, Josie Ursini‐SiegeliD, Peter M. SiegeliD, , Ivan TopisirovićiD
Abstract
Mitochondrial electron transport flavoprotein (ETF) insufficiency causes metabolic diseases known as a multiple acyl-CoA dehydrogenase deficiency (MADD). In contrast to muscle, ETFDH is a non-essential gene in acute lymphoblastic leukemia NALM-6 cells, and its expression is reduced across human cancers. ETF insufficiency caused by decreased ETFDH expression limits flexibility of OXPHOS fuel utilization but paradoxically increases cancer cell bioenergetics and accelerates neoplastic growth by activation of the mTORC1/BCL-6/4E-BP1 axis. Collectively, these findings reveal that while ETF insufficiency is rare and has detrimental effects in non-malignant tissues, it is common in neoplasia, where ETFDH downregulation leads to bioenergetic and signaling reprogramming that accelerate neoplastic growth.
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