Astrocyte elevated gene-1 is a proliferation promoter in breast cancer via suppressing transcriptional factor FOXO1

被引:115
作者
Li, J. [2 ,3 ]
Yang, L. [1 ,3 ]
Song, L. [4 ]
Xiong, H. [1 ,3 ]
Wang, L. [1 ,3 ]
Yan, X. [2 ,3 ]
Yuan, J. [2 ,3 ]
Wu, J. [1 ,3 ]
Li, M. [1 ,3 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Microbiol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Biochem, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Key Lab Trop Dis Control, Minist Educ, Guangzhou 510080, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol So China, Guangzhou 510080, Guangdong, Peoples R China
关键词
AEG-1; FOXO1; p27(Kip1); p21(Cip1); Akt; breast cancer; TUMOR PROGRESSION; PROSTATE-CANCER; CELL-SURVIVAL; BCCIP-ALPHA; PROTEIN; METASTASIS; DEGRADATION; INTEGRATION; ACTIVATION; EXPRESSION;
D O I
10.1038/onc.2009.171
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
We have previously reported that astrocyte elevated gene-1 (AEG-1) was upregulated in human breast cancer. However, the biological function of AEG-1 in the development and progression of breast cancer remains to be clarified. In this study, we examined the effect of AEG-1 on cell proliferation and found that AEG-1 upregulation was significantly linked to increased Ki67 (P < 0.001). Ectopic expression of AEG-1 in MCF-7 and MDA-MB-435 breast cancer cells dramatically enhanced cell proliferation and their ability of anchorage-independent growth, whereas silencing endogenous AEG-1 with shRNAs inhibited cell proliferation and colony-forming ability of the cells on soft agar. Furthermore, these proliferative effects were significantly associated with decreases of p27(Kip1) and p21(Cip1) two key cell-cycle inhibitors. Moreover, we further demonstrated that AEG-1 could downregulate the transcriptional activity of FOXO1 by inducing its phosphorylation through the PI3K/Akt signaling pathway. These observations were further confirmed in clinical human primary breast cancer specimens, in which high-level expression of AEG-1 was inversely correlated with the expression of FOXO1. Taken together, our results provide the first demonstration of a novel mechanism by which AEG-1 induces proliferation of breast cancer cell, and our findings suggest that AEG-1 might play an important role in tumorigenesis of breast cancer. Oncogene (2009) 28, 3188-3196; doi: 10.1038/onc.2009.171; published online 27 July 2009
引用
收藏
页码:3188 / 3196
页数:9
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