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星形胶质细胞上调基因-1通过抑制转录因子FOXO1成为乳腺癌的增殖促进因子。

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

作者信息

Li J, Yang L, Song L, Xiong H, Wang L, Yan X, Yuan J, Wu J, Li M

机构信息

Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

Oncogene. 2009 Sep 10;28(36):3188-96. doi: 10.1038/onc.2009.171. Epub 2009 Jul 27.

Abstract

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 p27Kip1 and p21Cip1 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.

摘要

我们之前报道过,星形胶质细胞上调基因-1(AEG-1)在人类乳腺癌中表达上调。然而,AEG-1在乳腺癌发生发展中的生物学功能仍有待阐明。在本研究中,我们检测了AEG-1对细胞增殖的影响,发现AEG-1的上调与Ki67的增加显著相关(P<0.001)。在MCF-7和MDA-MB-435乳腺癌细胞中异位表达AEG-1显著增强了细胞增殖及其非锚定依赖性生长能力,而用短发夹RNA沉默内源性AEG-1则抑制了细胞增殖以及细胞在软琼脂上的集落形成能力。此外,这些增殖效应与两种关键细胞周期抑制剂p27Kip1和p21Cip1的减少显著相关。而且,我们进一步证明,AEG-1可通过PI3K/Akt信号通路诱导FOXO1磷酸化,从而下调其转录活性。这些观察结果在临床人类原发性乳腺癌标本中得到进一步证实,其中AEG-1的高水平表达与FOXO1的表达呈负相关。综上所述,我们的结果首次证明了AEG-1诱导乳腺癌细胞增殖的新机制,我们的研究结果表明AEG-1可能在乳腺癌的肿瘤发生中起重要作用。

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