| Literature DB >> 22751500 |
An-Jou Chen1, Ji-Hye Paik, Hailei Zhang, Sachet A Shukla, Richard Mortensen, Jian Hu, Haoqiang Ying, Baoli Hu, Jessica Hurt, Natalie Farny, Caroline Dong, Yonghong Xiao, Y Alan Wang, Pamela A Silver, Lynda Chin, Shobha Vasudevan, Ronald A Depinho.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22751500 PMCID: PMC3403014 DOI: 10.1101/gad.189001.112
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361