Moonlighting proteins in cancer

被引:53
作者
Min, Kyung-Won [1 ]
Lee, Seong-Ho [2 ]
Baek, Seung Joon [1 ]
机构
[1] Univ Tennessee, Coll Vet Med, Dept Biomed & Diagnost Sci, Knoxville, TN 37996 USA
[2] Univ Maryland, Coll Agr & Nat Resources, Dept Nutr & Food Sci, College Pk, MD 20742 USA
关键词
Moonlighting protein; Translocation; Multi-functional proteins; Dynamic proteins; MACROPHAGE INHIBITORY CYTOKINE-1; DRUG-ACTIVATED GENE-1; CADHERIN-MEDIATED ADHESION; SMALL-MOLECULE INHIBITORS; BETA SIGNALING PATHWAY; NF-KAPPA-B; TISSUE TRANSGLUTAMINASE; TRANSCRIPTION FACTOR; NUCLEAR-LOCALIZATION; CELL-SURVIVAL;
D O I
10.1016/j.canlet.2015.09.022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the 1980s, growing evidence suggested that the cellular localization of proteins determined their activity and biological functions. In a classical view, a protein is characterized by the single cellular compartment where it primarily resides and functions. It is now believed that when proteins appear in different subcellular locations, the cells surpass the expected activity of proteins given the same genomic information to fulfill complex biological behavior. Many proteins are recognized for having the potential to exist in multiple locations in cells. Dysregulation of translocation may cause cancer or contribute to poorer cancer prognosis. Thus, quantitative and comprehensive assessment of dynamic proteins and associated protein movements could be a promising indicator in determining cancer prognosis and efficiency of cancer treatment and therapy. This review will summarize these so-called moonlighting proteins, in terms of a coupled intracellular cancer signaling pathway. Determination of the detailed biological intracellular and extracellular transit and regulatory activity of moonlighting proteins permits a better understanding of cancer and identification of potential means of molecular intervention. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:108 / 116
页数:9
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