Knockdown of astrocyte elevated gene-1 inhibits proliferation and enhancing chemo-sensitivity to cisplatin or doxorubicin in neuroblastoma cells

被引:84
作者
Liu, Haiyan [1 ]
Song, Xianrang [2 ]
Liu, Chunxi [3 ]
Xie, Li [2 ]
Wei, Ling [2 ]
Sun, Ruopeng [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Pediat, Jinan 250100, Peoples R China
[2] Shandong Canc Hosp & Inst, Dept Canc Res Ctr, Jinan, Peoples R China
[3] Shandong Univ, Qilu Hosp, Lab Cardiovasc Remodeling & Funct Res, Jinan 250100, Peoples R China
来源
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH | 2009年 / 28卷
关键词
CANCER PROGRESSION; METASTASIS; EXPRESSION; SURVIVAL; PROTEIN; CLONING; SYSTEM; AEG-1;
D O I
10.1186/1756-9966-28-19
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Astrocyte elevated gene-1 (AEG-1) was originally characterized as a HIV-1-inducible gene in primary human fetal astrocyte. Recent studies highlight a potential role of AEG-1 in promoting tumor progression and metastasis. The aim of this study was to investigate if AEG-1 serves as a potential therapeutic target of human neuroblastoma. Methods: We employed RNA interference to reduce AEG-1 expression in human neuroblastoma cell lines and analyzed their phenotypic changes. Results: We found that the knockdown of AEG-1 expression in human neuroblastoma cells significantly inhibited cell proliferation and apoptosis. The specific downregulation induced cell arrest in the G(0)/G(1) phase of cell cycle. In the present study, we also observed a significant enhancement of chemo-sensitivity to cisplatin and doxorubicin by knockdown of AEG-1. Conclusion: Our study suggests that overexpressed AEG-1 enhance the tumorogenic properties of neuroblastoma cells. The inhibition of AEG-1 expression could be a new adjuvant therapy for neuroblastoma.
引用
收藏
页数:9
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