A CDC20-APC/SOX2 Signaling Axis Regulates Human Glioblastoma Stem-like Cells

被引:87
作者
Mao, Diane D. [1 ]
Gujar, Amit D. [1 ]
Mahlokozera, Tatenda [1 ,2 ]
Chen, Ishita [1 ]
Pan, Yanchun [1 ]
Luo, Jingqin [3 ]
Brost, Taylor [4 ]
Thompson, Elizabeth A. [1 ]
Turski, Alice [1 ]
Leuthardt, Eric C. [1 ]
Dunn, Gavin P. [1 ,5 ,6 ,7 ,8 ]
Chicoine, Michael R. [1 ,5 ]
Rich, Keith M. [1 ,5 ]
Dowling, Joshua L. [1 ,5 ]
Zipfel, Gregory J. [1 ,5 ]
Dacey, Ralph G. [1 ,5 ]
Achilefu, Samuel [9 ]
Tran, David D. [5 ,10 ]
Yano, Hiroko [1 ,5 ,11 ,12 ]
Kim, Albert H. [1 ,5 ,11 ,13 ]
机构
[1] Washington Univ, Sch Med, Dept Neurol Surg, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Program Neurosci, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Med, Div Biostat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Program Mol Cell Biol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Siteman Canc Ctr, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Ctr Human Immunol, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Immunotherapy Programs, St Louis, MO 63110 USA
[8] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[9] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, Mol Imaging Ctr, St Louis, MO 63110 USA
[10] Washington Univ, Sch Med, Dept Med, Div Oncol, St Louis, MO 63110 USA
[11] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[12] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[13] Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO 63110 USA
来源
CELL REPORTS | 2015年 / 11卷 / 11期
关键词
INTEGRATED GENOMIC ANALYSIS; TUMOR-INITIATING CELLS; CYCLE PROGRESSION; SOX2; DIFFERENTIATION; INVASION; PATHWAY; GLIOMAS; IDH1; PHOSPHORYLATION;
D O I
10.1016/j.celrep.2015.05.027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glioblastoma harbors a dynamic subpopulation of glioblastoma stem-like cells (GSCs) that can propagate tumors in vivo and is resistant to standard chemoradiation. Identification of the cell-intrinsic mechanisms governing this clinically important cell state may lead to the discovery of therapeutic strategies for this challenging malignancy. Here, we demonstrate that the mitotic E3 ubiquitin ligase CDC20-anaphase-promoting complex (CDC20-APC) drives invasiveness and self-renewal in patient tumor-derived GSCs. Moreover, CDC20 knockdown inhibited and CDC20 overexpression increased the ability of human GSCs to generate brain tumors in an orthotopic xenograft model in vivo. CDC20-APC control of GSC invasion and self-renewal operates through pluripotency-related transcription factor SOX2. Our results identify a CDC20-APC/SOX2 signaling axis that controls key biological properties of GSCs, with implications for CDC20-APC-targeted strategies in the treatment of glioblastoma.
引用
收藏
页码:1809 / 1821
页数:13
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