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
相关论文
共 73 条
[21]   Classification and diagnostic prediction of cancers using gene expression profiling and artificial neural networks [J].
Khan, J ;
Wei, JS ;
Ringnér, M ;
Saal, LH ;
Ladanyi, M ;
Westermann, F ;
Berthold, F ;
Schwab, M ;
Antonescu, CR ;
Peterson, C ;
Meltzer, PS .
NATURE MEDICINE, 2001, 7 (06) :673-679
[22]   Cooperative DNA binding with AP-1 proteins is required for transformation by EWS-Ets fusion proteins [J].
Kim, S ;
Denny, CT ;
Wisdom, R .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (07) :2467-2478
[23]   NR0B1 is required for the oncogenic phenotype mediated by EWS/FLI in Ewing's sarcoma [J].
Kinsey, Michelle ;
Smith, Richard ;
Lessnick, Stephen L. .
MOLECULAR CANCER RESEARCH, 2006, 4 (11) :851-859
[24]   EWS/FLI and Its Downstream Target NR0B1 Interact Directly to Modulate Transcription and Oncogenesis in Ewing's Sarcoma [J].
Kinsey, Michelle ;
Smith, Richard ;
Iyer, Anita K. ;
McCabe, Edward R. B. ;
Lessnick, Stephen L. .
CANCER RESEARCH, 2009, 69 (23) :9047-9055
[25]   Phosphorylation of Ewing's sarcoma protein (EWS) and EWS-Fli1 in response to DNA damage [J].
Klevernic, Iva V. ;
Morton, Simon ;
Davis, Roger J. ;
Cohen, Philip .
BIOCHEMICAL JOURNAL, 2009, 418 :625-634
[26]   The splicing factor U1C represses EWS/FLI-mediated transactivation [J].
Knoop, LL ;
Baker, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24865-24871
[27]   EWS/FLI alters 5′-splice site selection [J].
Knoop, LL ;
Baker, SJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (25) :22317-22322
[28]   Context matters: The hen or egg problem in Ewing's sarcoma [J].
Kovar, H .
SEMINARS IN CANCER BIOLOGY, 2005, 15 (03) :189-196
[29]  
Kovar H, 1996, CELL GROWTH DIFFER, V7, P429
[30]   Regulation of Ets function by protein-protein interactions [J].
Li, RZ ;
Pei, HP ;
Watson, DK .
ONCOGENE, 2000, 19 (55) :6514-6523