Over-expression of AEG-1 significantly associates with tumour aggressiveness and poor prognosis in human non-small cell lung cancer

被引:109
作者
Song, Libing [1 ]
Li, Wen [2 ]
Zhang, Huizhong [3 ]
Liao, Wenting
Dai, Ting [4 ]
Yu, Chunping
Ding, Xiaofan [4 ]
Zhang, Lanjun [5 ]
Li, Jun
机构
[1] Sun Yat Sen Univ, Dept Expt Res, Ctr Canc, State Key Lab Oncol So China, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Lab Dept Surg, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Dept Pathol, Ctr Canc, Guangzhou 510060, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Dept Biochem, Zhongshan Sch Med, Guangzhou 510080, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Dept Thorac Surg, Ctr Canc, State Key Lab Oncol So China, Guangzhou 510060, Guangdong, Peoples R China
关键词
AEG-1; non-small cell lung cancer; aggressiveness; prognosis; ASTROCYTE-ELEVATED GENE-1; FACTOR-KAPPA-B; MESENCHYMAL TRANSITION; UP-REGULATION; INVASIVE PHENOTYPE; BREAST-CANCER; C-REL; METASTASIS; ACTIVATION; PROGRESSION;
D O I
10.1002/path.2595
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Astrocyte elevated gene 1 (AEG-1), a novel oncoprotein, has been implicated in oncogenesis and cancer progression in various types of human cancers. The clinical significance and biological role of AEG-1 in non-small cell lung cancer (NSCLC), however, remain unclear. In the present study, we found that the expression of AEG-1 was markedly up-regulated in NSCLC cell lines and NSCLC tissues at the level of both transcription and translation. Ectopically expressed AEG-1 enhanced the migratory and invasive abilities of NSCLC cells, whereas knockdown of endogenous AEG-1 by specific shRNAs significantly inhibited these abilities. The function of AEG-1 on metastasis modulation was associated with the activation of the PI3K-Akt and NF-kappa B signalling pathways. Furthermore, we showed high expression of AEG-1 in 99/200 (49.5%) paraffin-embedded archival NSCLC specimens. Moreover, statistical analysis displayed a significant correlation in AEG-1 expression with the clinical stage (p < 0.001), T classification (p = 0.001), N classification (P = 0.015), distant metastasis (p = 0.004) and differentiation (p = 027). Patients with higher AEG-1 expression had an overall shorter survival time, whereas patients with lower expression of AEG-1 had a better survival time. Multivariate analysis suggested that AEG-1 expression might be an independent prognostic indicator for the survival of NSCLC patients. Taken together, our results suggest that elevated expression of AEG-1 plays an important role in the aggressiveness of NSCLC, leading to a poor clinical outcome. Copyright (C) 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:317 / 326
页数:10
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