Oncogenic Partnerships: EWS-FLI1 Protein Interactions Initiate Key Pathways of Ewing's Sarcoma

被引:109
作者
Erkizan, Hayriye V. [1 ,2 ]
Uversky, Vladimir N. [3 ,4 ]
Toretsky, Jeffrey A. [1 ,2 ]
机构
[1] Georgetown Univ, Lombardi Comprehens Canc Ctr, Dept Oncol, Washington, DC 20007 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Ctr, Dept Pediat, Washington, DC 20007 USA
[3] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Ctr Computat Biol & Bioinformat, Inst Intrinsically Disordered Prot Res, Indianapolis, IN USA
[4] Russian Acad Sci, Inst Biol Instrumentat, Pushchino 142292, Moscow Region, Russia
基金
美国国家科学基金会;
关键词
RNA-POLYMERASE-II; PRECLINICAL TESTING PROGRAM; FUSION PROTEIN; DNA-BINDING; FUNCTIONAL-ANALYSIS; INTERFERING RNA; TUMOR-GROWTH; HELICASE-A; EWS/FLI-1; TARGET;
D O I
10.1158/1078-0432.CCR-09-2261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeted therapy for cancer, which is specifically directed toward the cancer without any potential for effects outside of controlling the tumor, is a gold standard for treatment. Ewing's sarcoma contains the potential target EWS-FLI1, as a result of a pathognomonic chromosomal translocation. The EWS-FLI1 fusion protein includes the EWS domain, a potent transcriptional activator alongside the highly conserved FLI1 ets DNA-binding domain. Because of the combination of these domains, the EWS-FLI1 fusion protein acts as an aberrant transcription factor whose expression results in cellular transformation. EWS-FLI1 functions by binding to normal cellular protein partners in transcription and splicing, similar to how a virus would corrupt normal cellular machinery for virion production. Therefore, understanding the protein-protein interactions of EWS-FLI1 and the pathways that are regulated by these partnerships will inform both oncogenesis and therapeutics. This review describes the known protein partners and transcriptional targets of EWS-FLI1, while proposing strategies for exploiting these partnerships with targeted therapy. Clin Cancer Res; 16(16); 4077-83. (C) 2010 AACR.
引用
收藏
页码:4077 / 4083
页数:7
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