PKR, apoptosis and cancer

被引:167
作者
Jagus, R [1 ]
Joshi, B
Barber, GN
机构
[1] Univ Maryland, Maryland Biotechnol Inst, Ctr Med Biotechnol, Baltimore, MD 21201 USA
[2] Univ Maryland, Maryland Biotechnol Inst, Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[3] Emory Univ, Sch Med, Winship Canc Ctr, Atlanta, GA 30322 USA
关键词
PKR; eIF2; alpha; apoptosis; translational regulation; breast cancer;
D O I
10.1016/S1357-2725(98)00136-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The double-stranded (ds) RNA-regulated serine/threonine protein kinase, PKR, is an interferon-inducible enzyme of widespread occurrence in mammalian cells. PKR is activated by dsRNA via a mechanism involving autophosphorylation Once activated, the enzyme phosphorylates the alpha-subunit of protein synthesis initiation factor eIF2, thereby inhibiting translation. Accumulating data suggest that PKR has additional substrates, and that the kinase may also regulate gene transcription and signal transduction pathways. Although PKR plays an important role in mediating the antiviral effects of interferons, PKR is also implicated in regulating cell proliferation in uninfected cells and may have a tumor suppressor function under normal conditions. Studies of human malignancies and tumor cell lines suggest that, in general, patients bearing tumors with a higher PKR content have a more favorable prognosis. However, in human breast carcinoma cells, dysregulation of PKR may be associated with the establishment or maintenance of the transformed state. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:123 / 138
页数:16
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