F-box protein interactions with the hallmark pathways in cancer

被引:65
|
作者
Randle, Suzanne J. [1 ]
Laman, Heike [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Tennis Court Rd, Cambridge CB2 1QP, England
基金
英国生物技术与生命科学研究理事会;
关键词
Ubiquitination; F-box proteins; E3 ubiquitin ligases; Signalling; Cancer hallmarks; E3 UBIQUITIN LIGASE; EPITHELIAL-MESENCHYMAL TRANSITION; PROTEASOME-DEPENDENT DEGRADATION; ANAPHASE-PROMOTING COMPLEX; CYCLIN D1 DEGRADATION; EMBRYONIC STEM-CELLS; NF-KAPPA-B; BETA-TRCP; DNA-DAMAGE; AURORA-B;
D O I
10.1016/j.semcancer.2015.09.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
F-box proteins (FBP) are the substrate specifying subunit of Skp1-Cul1-FBP (SCF)-type E3 ubiquitin ligases and are responsible for directing the ubiquitination of numerous proteins essential for cellular function. Due to their ability to regulate the expression and activity of oncogenes and tumour suppressor genes, FBPs themselves play important roles in cancer development and progression. In this review, we provide a comprehensive overview of FBPs and their targets in relation to their interaction with the hallmarks of cancer cell biology, including the regulation of proliferation, epigenetics, migration and invasion, metabolism, angiogenesis, cell death and DNA damage responses. Each cancer hallmark is revealed to have multiple FBPs which converge on common signalling hubs or response pathways. We also highlight the complex regulatory interplay between SCF-type ligases and other ubiquitin ligases. We suggest six highly interconnected FBPs affecting multiple cancer hallmarks, which may prove sensible candidates for therapeutic intervention. (C) 2015 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license.
引用
收藏
页码:3 / 17
页数:15
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