Astrocyte elevated gene-1 contributes to the pathogenesis of neuroblastoma

被引:100
作者
Lee, S-G [1 ,2 ]
Jeon, H-Y [1 ]
Su, Z-Z [1 ]
Richards, J. E. [1 ]
Vozhilla, N. [1 ]
Sarkar, D. [1 ,2 ,4 ]
Van Maerken, T. [3 ]
Fisher, P. B. [1 ,2 ,4 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Human & Mol Genet, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Sch Med, VCU Massey Canc Ctr, Richmond, VA 23298 USA
[3] Ghent Univ Hosp, Ctr Med Genet, B-9000 Ghent, Belgium
[4] Virginia Commonwealth Univ, Sch Med, VCU Inst Mol Med, Richmond, VA 23298 USA
关键词
neuroblastoma; AEG-1; MYCN; PI3K; Akt; RAPID SUBTRACTION HYBRIDIZATION; PHOSPHATIDYLINOSITOL; 3-KINASE; N-MYC; C-MYC; CANCER PROGRESSION; TUMOR PROGRESSION; BREAST-CANCER; EXPRESSION; PATHWAY; CELLS;
D O I
10.1038/onc.2009.93
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
Neuroblastoma, derived from neural crest progenitor cells, is the most common extracranial solid tumor of childhood. Astrocyte elevated gene-1 (AEG-1) is a primary mediator of tumor progression and metastasis in several human cancers. In this study, we investigated the potential contribution of AEG-1 in human neuroblastoma pathogenesis. AEG-1 expression was significantly elevated in neuroblastoma patient-derived samples and neuroblastoma cell lines as compared with normal peripheral nerve tissues, normal astrocytes and immortalized melanocytes. Knockdown of AEG-1 by small interfering RNA reduced the tumorigenic properties of highly aggressive neuroblastoma cells. Conversely, over-expression of AEG-1 enhanced proliferation and expression of the transformed state in less aggressive neuroblastoma cells through activation of the phosphatidylinositol 3-kinase-Akt-signaling pathway and stabilization of MYCN. These provocative results indicate that AEG-1 may play a crucial role in the pathogenesis of neuroblastoma and could represent a potential target for therapeutic intervention. Oncogene (2009) 28, 2476-2484; doi:10.1038/onc.2009.93; published online 18 May 2009
引用
收藏
页码:2476 / 2484
页数:9
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