A critical role of Sonic Hedgehog signaling in maintaining the tumorigenicity of neuroblastoma cells

被引:42
|
作者
Mao, Ling [1 ]
Xia, Yuan-Peng [1 ]
Zhou, Yu-Nan [1 ]
Dai, Ruo-Lian [1 ]
Yang, Xue [1 ]
Duan, Shu-Jie [1 ]
Qiao, Xian [1 ]
Mei, Yuan-Wu [1 ]
Hu, Bo [1 ]
Cui, Hongjuan [2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Neurol, Union Hosp, Wuhan 430074, Peoples R China
[2] Univ Toledo, Coll Med, Dept Biochem & Canc Biol, Toledo, OH 43606 USA
来源
CANCER SCIENCE | 2009年 / 100卷 / 10期
基金
中国国家自然科学基金;
关键词
NEURAL CREST CELLS; CANCER STEM-CELLS; FLOOR PLATE; INHIBITION; GLI2; PROLIFERATION; CYCLOPAMINE; PATHWAY; DIFFERENTIATION; TRANSDUCTION;
D O I
10.1111/j.1349-7006.2009.01262.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulated evidence suggests a major role for the activation of the Sonic Hedgehog (SHH) signaling pathway in the development of neural crest stem cells that give rise to the sympathetic nervous system. We therefore investigated the involvement of SHH signaling in the pathogenesis of neuroblastoma, a common childhood malignant tumor of the sympathetic nervous system. Human neuroblastoma cell lines and a majority of primary neuroblastoma specimens showed high-level expression of the pathway targets and components, indicating persistent activation of the SHH pathway. All of the neuroblastoma cell lines we examined expressed significant levels of SHH ligand, suggesting an autocrine, ligand-dependent activation of the SHH pathway in neuroblastoma cells. Inhibition of SHH signaling by cyclopamine induced apoptosis and blocked proliferation in all major types of neuroblastoma cells, and abrogated the tumorigenicity of neuroblastoma cells. Moreover, the knockdown of GLI2 in neuroblastoma BE (2)-C and SK-N-DZ cell lines resulted in the inhibition of colony formation. Our study has revealed a molecular mechanism for the persistent activation of the SHH pathway which promotes the development of neuroblastoma, and suggests a new approach for the treatment of this childhood malignant tumor. (Cancer Sci 2009; 100: 1848-1855).
引用
收藏
页码:1848 / 1855
页数:8
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