(L5213) DEPTOR Tyrosine Phosphorylation: A Novel Molecular Switch Involved in mTOR Activity

Laurence Gagné (CHU de Québec Research Center CHU de Québec-Université Laval)| Nadine Morin (CHU de Québec Research Center CHU de Québec-Université Laval)| Noémie Lavoie (CHU de Québec Research Center CHU de Québec-Université Laval)| Jean-Philippe Lambert (CHU de Québec Research Center CHU de Québec-Université Laval)| Nicolas Bisson (CHU de Québec Research Center CHU de Québec-Université Laval)| Frédérick Mallette (CHU de Québec Research Center CHU de Québec-Université Laval)| Marc-Étienne Huot (CHU de Québec Research Center CHU de Québec-Université Laval)

Dysregulated mTOR (mechanistic Target Of Rapamycin) is a potent tumor growth inducer known to promote cancer cell proliferation and survival. Its activity can be regulated by numerous factors composing the PTEN/PI3K/AKT canonical pathway, which are often mutated in cancer. However, in a subset of cancer showing a constitutively activated mTOR, there is no alteration within the canonical activation pathway, suggesting different activation mechanism. We previously discovered several post-translational modifications (PTMs) on DEP domain-containing mTOR-interacting protein (DEPTOR), an endogenous regulator of the two mTOR complexes (mTORC1 and mTORC2). Still, the mechanism by which these PTMs regulate DEPTOR ability to shut down mTOR complexes remains ill-defined. Studies have only shown that DEPTOR is phosphorylated on serine (S286/287/291/293/299) under high energy level condition, leading to its degradation by the ubiquitin/proteasome system. Unlike this irreversible regulatory mechanism, we have recently identified another PTM, a tyrosine phosphorylation that affects DEPTOR inhibitory functions. We found that phosphorylation of DEPTOR tyrosine 289 increase its stability, while promoting DEPTOR dissociation from mTORC1&2, leading to a rapid and sustain increase in mTORC1&2 activity. To identify the upstream signaling pathway causing tyrosine 289 phosphorylation, we performed mass spectrometry analysis, as well as a small drug screening of different tyrosine kinase inhibitors. Using these combined methods, we identify Syk (Spleen tyrosine kinase), whose expression levels correlate with levels of tyrosine 289 phosphorylation. We also found that Syk-induced phosphorylation of DEPTOR was regulated by the EphB2 receptor. Our findings uncovered a new mechanism regulating mTOR activity, which explains the increased mTOR activity in cancer with unaffected PTEN/PI3K/AKT regulatory pathways. Better understanding of this mTOR/DEPTOR regulatory pathway could allow the development of a new therapeutic approach to inhibit mTOR associated cancer progression.