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.
A CDC20-APC/SOX2 Signaling Axis Regulates Human Glioblastoma Stem-like Cells.
CDC20-APC/SOX2信号轴调控人类胶质母细胞瘤干细胞样细胞。
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| 期刊: | Cell Reports | 影响因子: | 6.900 |
| 时间: | 2015 | 起止号: | 2015 Jun 23; 11(11):1809-21 |
| doi: | 10.1016/j.celrep.2015.05.027 | ||
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