PDCD4 limits prooncogenic neuregulin-ErbB signaling

The neuregulins and their ErbB/HER receptors play essential roles in mammalian development and tissue homeostasis. In addition, deregulation of their function has been linked to the pathogenesis of diseases such as cancer or schizophrenia. These circumstances have stimulated research into the biology of this ligand-receptor system. Here we show the identification of programmed cell death protein-4 (PDCD4) as a novel neuregulin-ErbB signaling mediator. Phosphoproteomic analyses identified PDCD4 as protein whose phosphorylation increased in cells treated with neuregulin. Mutagenesis experiments defined serine 67 of PDCD4 as a site whose phosphorylation increased upon activation of neuregulin receptors. Phosphorylation of that site promoted degradation of PDCD4 by the proteasome, which depended on exit of PDCD4 from the nucleus to the cytosol. Mechanistic studies defined mTORC1 and ERK1/2 as routes implicated in neuregulin-induced serine 67 phosphorylation and PDCD4 degradation. Functionally, PDCD4 regulated several important biological functions of neuregulin, such as proliferation, migration, or invasion.

Automated summary

Neuregulins and their ErbB/HER receptors are important in mammalian development and tissue homeostasis, with PDCD4 identified as a novel mediator in neuregulin-ErbB signaling. Phosphorylation of PDCD4 at serine 67 is shown to promote its degradation and regulate important biological functions of neuregulin, such as proliferation, migration, and invasion, through mTORC1 and ERK1/2 pathways.