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               <mods:identifier type="citation">Nat Commun. 2016;7:10438.</mods:identifier>
               <mods:identifier type="doi">10.1038/ncomms10438</mods:identifier>
               <mods:identifier type="e-issn">2041-1723</mods:identifier>
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               <mods:abstract>The levels, regulation and prognostic value of p21 in head and neck squamous cell carcinomas (HNSCC) has been puzzling for years. Here, we report a new mechanism of regulation of p21 by the mTORC1/4E-BP1 pathway. We find that non-phosphorylated 4E-BP1 interacts with p21 and induces its degradation. Accordingly, hyper-activation of mTORC1 results in phosphorylation of 4E-BP1 and stabilization of p21. In HNSCC, p21 levels strongly correlate with mTORC1 activity but not with p53 status. Finally, clinical data indicate that HNSCC patients with p21 and phospho-S6-double-positive tumours present a better disease-specific survival. We conclude that over-activation of the mTORC1/4E-BP1/p21 pathway is a frequent and clinically relevant alteration in HNSCC.</mods:abstract>
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                  <mods:title>Stabilization of p21 by mTORC1/4E-BP1 predicts clinical outcome of head and neck cancers</mods:title>
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