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Fig. 7. A novel pathway involving mTOR and Mdm2 signals cell survival. Upon
Hgf stimulation, Met triggers the nuclear translocation of Mdm2 by activating
the PI3K-Akt pathway. In addition, Met enhances Mdm2 translation by acting on
Akt-mTOR via PI3K. The relevance of this mechanism for Met-triggered cell
survival has been genetically and pharmacologically demonstrated. Blocking a
single step of this pathway alters the cell survival/death balance in
embryonic cells.