Astrocyte elevated gene-1 (AEG-1) is a target gene of oncogenic Ha-ras requiring phosphatidylinositol 3-kinase and c-Myc

被引:200
|
作者
Lee, Seok-Geun
Su, Zao-Zhong
Emdad, Luni
Sarkar, Devanand
Fisher, Paul B. [1 ]
机构
[1] Columbia Univ, Med Ctr, Coll Phys & Surg, Dept Urol, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Coll Phys & Surg, Dept Neurosurg, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Coll Phys & Surg, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
关键词
tumor-promoting gene; signaling pathway; transcription; RAPID SUBTRACTION HYBRIDIZATION; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; CELL-CYCLE; TRANSCRIPTIONAL REGULATION; SIGNALING PATHWAY; EPITHELIAL-CELLS; PROTEIN-KINASES; BINDING-PROTEIN; CANCER-THERAPY;
D O I
10.1073/pnas.0608386103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It is well established that Ha-ras and c-myc genes collaborate in promoting transformation, tumor progression, and metastasis. However, the precise mechanism underlying this cooperation remains unclear. In the present study, we document that astrocyte elevated gene-1 (AEG-1) is a downstream target molecule of Ha-ras and c-myc, mediating their tumor-promoting effects. AEG-1 expression is elevated in diverse neoplastic states, it cooperates with Ha-ras to promote transformation, and its overexpression augments invasion of transformed cells, demonstrating its functional involvement in Ha-ras-mediated tumorigenesis. We now document that AEG-1 expression is markedly induced by oncogenic Ha-ras, activating the phosphatidylinositol 3-kinase signaling pathway that augments binding of c-Myc to key E-box elements in the AEG-1 promoter, thereby regulating AEG-1 transcription. In addition, Ha-ras-mediated colony formation is inhibited by AEG-1 siRNA. This is a demonstration that Ha-ras activation of a tumor-promoting gene is regulated directly by c-Myc DNA binding via phosphatidylinositol 3-kinase signaling, thus revealing a previously uncharacterized mechanism of Ha-ras-mediated oncogenesis through AEG-1.
引用
收藏
页码:17390 / 17395
页数:6
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