Targeting Glioma Stem Cells by Functional Inhibition of a Prosurvival OncomiR-138 in Malignant Gliomas

被引:89
作者
Chan, Xin Hui Derryn [1 ]
Nama, Srikanth [1 ]
Gopal, Felicia [1 ]
Rizk, Pamela [1 ]
Ramasamy, Srinivas [1 ]
Sundaram, Gopinath [1 ]
Ow, Ghim Siong [2 ]
Vladimirovna, Ivshina Anna [2 ]
Tanavde, Vivek [2 ]
Haybaeck, Johannes [3 ]
Kuznetsov, Vladimir [2 ]
Sampath, Prabha [1 ,4 ]
机构
[1] Agcy Sci Technol & Res, Inst Med Biol, Singapore 138648, Singapore
[2] Agcy Sci Technol & Res, Bioinformat Inst, Singapore 138671, Singapore
[3] Med Univ Graz, Dept Neuropathol, A-8036 Graz, Austria
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
来源
CELL REPORTS | 2012年 / 2卷 / 03期
关键词
C-MYC; TUMOR-GROWTH; IN-VIVO; GLIOBLASTOMA; EXPRESSION; BRAIN; IDENTIFICATION; MICRORNA-21; ARREST; OVEREXPRESSION;
D O I
10.1016/j.celrep.2012.07.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Malignant gliomas are the most aggressive forms of brain tumors, associated with high rates of morbidity and mortality. Recurrence and tumorigenesis are attributed to a subpopulation of tumor-initiating glioma stem cells (GSCs) that are intrinsically resistant to therapy. Initiation and progression of gliomas have been linked to alterations in microRNA expression. Here, we report the identification of microRNA-138 (miR-138) as a molecular signature of GSCs and demonstrate a vital role for miR-138 in promoting growth and survival of bona fide tumor-initiating cells with self-renewal potential. Sequence-specific functional inhibition of miR-138 prevents tumorsphere formation in vitro and impedes tumorigenesis in vivo. We delineate the components of the miR-138 regulatory network by loss-of-function analysis to identify specific regulators of apoptosis. Finally, the higher expression of miR-138 in GSCs compared to non-neoplastic tissue and association with tumor recurrence and survival highlights the clinical significance of miR-138 as a prognostic biomarker and a therapeutic target for treatment of malignant gliomas.
引用
收藏
页码:591 / 602
页数:12
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