Modulation of the cell growth regulator mTOR by Epstein-Barr virus-encoded LMP2A

被引:96
作者
Moody, CA
Scott, RS
Amirghahari, N
Nathan, CA
Young, LS
Dawson, CW
Sixbey, JW
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Ctr Mol & Tumor Virol, Shreveport, LA 71130 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, Shreveport, LA 71130 USA
[3] Louisiana State Univ, Hlth Sci Ctr, Dept Otolaryngol Head & Neck Surg, Shreveport, LA 71130 USA
[4] Louisiana State Univ, Hlth Sci Ctr, Feist Weiller Canc Ctr, Shreveport, LA 71130 USA
[5] Canc Res UK, Inst Canc Studies, Birmingham B15 2TT, W Midlands, England
关键词
D O I
10.1128/JVI.79.9.5499-5506.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Control of translation initiation is one means by which cells regulate growth and proliferation, with components of the protein-synthesizing machinery having oncogenic potential. Expression of latency protein LMP2A by the human tumor virus Epstein-Barr virus (EBV) activates phosphatidylinositol 3-kinase/Akt located upstream of an essential mediator of growth signals, mTOR (mammalian target of rapamycin). We show that mTOR is activated by expression of LMP2A in carcinoma cells, leading to wortmannin- and rapamycin-sensitive inhibition of the negative regulator of translation, eukaryotic initiation factor 4E-binding protein 1, and increased c-Myc protein translation. Intervention by this DNA tumor virus in cellular translational controls is likely to be an integral component of EBV tumorigenesis.
引用
收藏
页码:5499 / 5506
页数:8
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