Small molecule therapeutics targeting F-box proteins in cancer

被引:22
|
作者
Liu, Yuan [1 ]
Mallampalli, Rama K. [1 ,2 ]
机构
[1] Univ Pittsburgh, Ctr Excellence, Acute Lung Injury, Dept Med, Pittsburgh, PA 15213 USA
[2] Vet Affairs Pittsburgh Healthcare Syst, Med Specialty Serv Line, Pittsburgh, PA 15240 USA
基金
美国国家卫生研究院;
关键词
Ubiquitin; E3; ligase; F-box protein; Small molecule inhibitor; Cancer; SCF UBIQUITIN-LIGASE; NF-KAPPA-B; CELL-CYCLE ARREST; PHOSPHORYLATION-DEPENDENT UBIQUITINATION; ANAPHASE PROMOTING COMPLEX/CYCLOSOME; TUMOR-SUPPRESSOR; BETA-TRCP; C-MYC; MEDIATED DEGRADATION; PROTEASOMAL DEGRADATION;
D O I
10.1016/j.semcancer.2015.09.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The ubiquitin proteasome system (UPS) plays vital roles in maintaining protein equilibrium mainly through proteolytic degradation of targeted substrates. The archetypical SCF ubiquitin E3 ligase complex contains a substrate recognition subunit F-box protein that recruits substrates to the catalytic ligase core for its polyubiquitylation and subsequent proteasomal degradation. Several well-characterized F-box proteins have been demonstrated that are tightly linked to neoplasia. There is mounting information characterizing F-box protein-substrate interactions with the rationale to develop unique therapeutics for cancer treatment. Here we review that how F-box proteins function in cancer and summarize potential small molecule inhibitors for cancer therapy. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:105 / 119
页数:15
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