Journal of Biological Chemistry · 2019 · 29 citations · 32 references
Life SciencesCancer BiologyOncologyCell SignalingMolecular OncologySignal TransductionBone Morphogenetic Protein SignalingCancer Cell SignalingGrowth Factor SignalingOncogenic Signaling PathwaysBmp Signal TransductionSmad Signaling PathwaySmad-mediated Signal TransductionTransforming Growth Factor Beta Signaling ModulationTransforming Growth Factor-beta Signaling
, plays a key role in its Smad4-regulating activity. PDZK1IP1 knockdown enhanced the expression of the TGF-β target genes Smad7 and prostate transmembrane protein androgen-induced (TMEPAI) upon TGF-β stimulation. In contrast, PDZK1IP1 overexpression suppressed TGF-β-induced reporter activities, cell migration, and cell growth inhibition. In a xenograft tumor model in which TGF-β was previously shown to elicit tumor-promoting effects, PDZK1IP1 gain of function decreased tumor size and increased survival rates. Taken together, these findings indicate that PDZK1IP1 interacts with Smad4 and thereby suppresses the TGF-β signaling pathway.
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