Astrocyte Elevated Gene-1: Far More Than Just a Gene Regulated in Astrocytes

被引:92
作者
Sarkar, Devanand [2 ,3 ]
Emdad, Luni [4 ]
Lee, Seok-Geun [3 ]
Yoo, Byoung Kwon
Su, Zao-zhong
Fisher, Paul B. [1 ,2 ,3 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Human & Mol Genet, Richmond, VA 23298 USA
[2] Virginia Commonwealth Univ, Inst Mol Med, Richmond, VA 23298 USA
[3] Virginia Commonwealth Univ, Massey Canc Ctr, Sch Med, Richmond, VA 23298 USA
[4] Mt Sinai Sch Med, Dept Neurosurg, New York, NY USA
基金
美国国家卫生研究院;
关键词
CANCER PROGRESSION; TUMOR PROGRESSION; BREAST-CANCER; PROTEIN; IDENTIFICATION; ACTIVATION; OVEREXPRESSION; PROLIFERATION; HYBRIDIZATION; LYRIC/AEG-1;
D O I
10.1158/0008-5472.CAN-09-1846
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since its original cloning by subtraction hybridization in 2002, it is now evident that Astrocyte elevated gene-1 (AEG-1) is a key contributor to the carcinogenic process in diverse organs. AEG-1 protein expression is elevated in advanced stages of many cancers, which correlates with poor survival. In specific cancers, such as breast and liver cancer, the AEG-1 gene itself is amplified, further supporting a seminal role in tumorigenesis. Overexpression and inhibition studies both in in vitro and in in vivo models reveal the importance of AEG-1 in regulating multiple physiologically and pathologically relevant processes including proliferation, invasion, metastasis, and gene expression. AEG-1 is a single-pass transmembrane protein with multiple nuclear localization signals and no known domains or motifs. Although pertinent roles of AEG-1 in the carcinogenic process are established, its potential function (promotion of metastasis only versus functioning as a bona ride oncogene) as well as localization (cell surface versus nucleus) remain areas requiring further clarification. The present review critically evaluates what is currently known about AEG-1 and provides new perspectives relative to this intriguing molecule that may provide a rational target for intervening in the cancer phenotype. [Cancer Res 2009:69(22):8529-35]
引用
收藏
页码:8529 / 8535
页数:7
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