F-box proteins: Keeping the epithelial-to-mesenchymal transition (EMT) in check

被引:103
作者
Diaz, Victor M. [1 ,2 ,3 ]
de Herreros, Antonio Garcia [1 ,2 ,3 ]
机构
[1] Inst Hosp Mar Invest Med IMIM, Programa Recerca Canc, C Doctor Aiguader 88, Barcelona, Spain
[2] Univ Pompeu Fabra, Dept Ciencies Expt & Salut, Barcelona, Spain
[3] Doctor Aiguader 88, E-08003 Barcelona, Spain
关键词
EMT; Snail; Twist; Zeb; F-box; Ubiquitination; Proteasome; Cancer; FBW7 UBIQUITIN LIGASE; E-CADHERIN REPRESSION; PHOSPHORYLATION-DEPENDENT DEGRADATION; TRANSCRIPTION FACTORS SNAIL; SCF-BETA-TRCP; NF-KAPPA-B; BREAST-CANCER; TUMOR-SUPPRESSOR; C-MYC; CELL-MIGRATION;
D O I
10.1016/j.semcancer.2015.10.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
F-box proteins are the key recognition subunit of multimeric E3 ubiquitin ligase complexes that participate in the proteasome degradation of specific substrates. In the last years, a discrete number of F-box proteins have been shown to regulate the epithelial-to-mesenchymal transition (EMT), a process defined by a rapid change of cell phenotype, the loss of epithelial characteristics and the acquisition of a more invasive phenotype. Specific EMT transcription factors (EMT-TFs), such as Snail, Slug, Twist and Zeb, control EMT induction both during development and in cancer. These EMT-TFs are short-lived proteins that are targeted to the proteasome system by specific F-box proteins, keeping them at low levels. F-box proteins also indirectly regulate the EMT process by controlling EMT inducers, such as Notch, c-Myc or mTOR. Here we summarize the role that these F-box proteins (Fbxw1, Fbxw7, Fbxl14, Fbxl5, Fbxo11 and Fbxo45) play in controlling EMT during development and cancer progression, a process dependent on post-translational modifications that govern their interaction with target proteins. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:71 / 79
页数:9
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