Genes & Development · 2012 · 112 citations · 54 references
Life SciencesMolecular BiologyOncologyGene ExpressionMolecular OncologySignal TransductionCancer Cell SignalingMicrorna BiologyMicrorna-mediated RegulationRna InterferenceSignal Transduction In CancerTumor Suppressor GenesEpistasis AnalysisMicrorna In CancerMicrorna Regulation In CancerRna-binding Protein InteractionsTumor Suppression PathwaysTumor Suppressor NetworksTumor Suppressor P53Tumor Suppressor Pathways
Multidimensional cancer genome analysis and validation has defined Quaking (QKI), a member of the signal transduction and activation of RNA (STAR) family of RNA-binding proteins, as a novel glioblastoma multiforme (GBM) tumor suppressor. Here, we establish that p53 directly regulates QKI gene expression, and QKI protein associates with and leads to the stabilization of miR-20a; miR-20a, in turn, regulates TGFβR2 and the TGFβ signaling network. This pathway circuitry is substantiated by in silico epistasis analysis of its components in the human GBM TCGA (The Cancer Genome Atlas Project) collection and by their gain- and loss-of-function interactions in in vitro and in vivo complementation studies. This p53-QKI-miR-20a-TGFβ pathway expands our understanding of the p53 tumor suppression network in cancer and reveals a novel tumor suppression mechanism involving regulation of specific cancer-relevant microRNAs.
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A microRNA component of the p53 tumour suppressor network
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