Dysregulation of protein synthesis and disease

被引:68
作者
Le Quesne, John P. C. [2 ]
Spriggs, Keith A. [1 ]
Bushell, Martin [1 ]
Willis, Anne E. [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Ctr Biomol Sci, Nottingham NG7 2RD, England
[2] Li Ka Shing Ctr, Cambridge Res Inst, Canc Res UK, Cambridge CB2 0RE, England
基金
英国生物技术与生命科学研究理事会;
关键词
protein synthesis; cancer; neurological diseases; micro RNA; IRES; 5 '-UTR; translation; INTERNAL RIBOSOME ENTRY; TRANSFER-RNA-SYNTHETASE; MICRORNA EXPRESSION PROFILES; IRES-MEDIATED TRANSLATION; TUMOR-SUPPRESSOR GENE; INITIATION-FACTOR; 4E; TRANS-ACTING FACTORS; C-MYC-IRES; MESSENGER-RNAS; MIR-200; FAMILY;
D O I
10.1002/path.2627
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The regulation of protein synthesis plays as important a role as transcriptional control in the control of gene expression. Once thought solely to act globally, translational control has now been shown to be able to control the expression of most genes specifically. Dysregulation of this process is associated with a range of pathological conditions, notably cancer and several neurological disorders, and can occur in many ways. These include alterations in the expression of canonical initiation factors, mutations in regulatory mRNA sequence elements in 5' and 3' untranslated regions (UTRs), such as upstream open reading frames (uORFs), internal ribosome entry segments (IRESs) and micro-RNA (miR) target sites, and the altered expression of trans-acting protein factors that bind to and regulate these elements. Translational control is increasingly open for study in both fresh and fixed tissue, and this rapidly developing field is yielding useful diagnostic and prognostic tools that will hopefully provide new targets for effective treatments. Copyright (C) 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:140 / 151
页数:12
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