SOX9-mediated upregulation of LGR5 is important for glioblastoma tumorigenicity

被引:21
作者
Hiraoka, Koji [1 ]
Hayashi, Tomoatsu [1 ]
Kaneko, Ryusuke [1 ]
Nasu-Nishimura, Yukiko [1 ]
Koyama-Nasu, Ryo [1 ]
Kawasaki, Yoshihiro [1 ]
Akiyama, Tetsu [1 ]
机构
[1] Univ Tokyo, Lab Mol & Genet Informat, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
Glioblastoma; Leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5); Sry-related high-mobility group (HMG) box 9 (SOX9); Tumorigenicity; COUPLED RECEPTOR GPR49; STEM-CELLS; WNT/BETA-CATENIN; PROLIFERATION; GLIOMA;
D O I
10.1016/j.bbrc.2015.03.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
LGR5 plays an important role in the self-renewal of stem cells and is used as a marker identifying self-renewing stem cells in small intestine and hair follicles. Moreover, LGR5 has been reported to be over-expressed in several cancers. SOX9 is a transcription factor that plays a key role in development, differentiation and lineage commitment in various tissues. It has also been reported that SOX9 is over-expressed in a variety of cancers and contributes to their malignant phenotype. Here we show that LGR5 is required for the tumorigenicity of glioblastoma cells. We further show that SOX9 is upregulated in glioblastoma cells and directly enhances the expression of LGR5. We also demonstrate that knockdown of SOX9 suppresses the proliferation and tumorigenicity of glioblastoma cells. These results suggest that SOX9-mediated transcriptional regulation of LGR5 is critical for the tumorigenicity of glioblastoma cells. We speculate that the SOX9-LGR5 pathway could be a potentially promising target for the therapy of glioblastoma. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
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