STAR RNA-binding protein Quaking suppresses cancer via stabilization of specific miRNA

被引:105
作者
Chen, An-Jou [1 ,2 ,3 ]
Paik, Ji-Hye [1 ,2 ,3 ]
Zhang, Hailei [1 ,2 ]
Shukla, Sachet A. [1 ,2 ]
Mortensen, Richard [4 ]
Hu, Jian [1 ,2 ,3 ,5 ]
Ying, Haoqiang [1 ,2 ,3 ,5 ]
Hu, Baoli [1 ,2 ,5 ]
Hurt, Jessica [6 ]
Farny, Natalie [6 ]
Dong, Caroline [1 ,2 ]
Xiao, Yonghong [1 ,2 ]
Wang, Y. Alan [1 ,2 ,5 ]
Silver, Pamela A. [6 ]
Chin, Lynda [1 ,2 ,5 ,7 ]
Vasudevan, Shobha [4 ]
DePinho, Ronald A. [1 ,2 ,3 ,8 ]
机构
[1] Harvard Univ, Sch Med, Belfer Inst Appl Canc Sci, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Med & Genet, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Canc, Boston, MA 02129 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77030 USA
[6] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Dept Dermatol, Brigham & Womens Hosp, Boston, MA 02115 USA
[8] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77030 USA
关键词
cancer; GBM; miRNA; p53; TGF beta; QKI; GROWTH-FACTOR-BETA; MESSENGER-RNA; SIGNAL-TRANSDUCTION; MIR-17-92; CLUSTER; TGF-BETA; P53; CELL; MICRORNAS; GENE; IDENTIFICATION;
D O I
10.1101/gad.189001.112
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 TGF beta R2 and the TGF beta 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-TGF beta 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.
引用
收藏
页码:1459 / 1472
页数:14
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