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本文引用的文献

1
Initial testing of a monoclonal antibody (IMC-A12) against IGF-1R by the Pediatric Preclinical Testing Program.儿科临床前测试计划对 IGF-1R 单克隆抗体(IMC-A12)的初步测试。
Pediatr Blood Cancer. 2010 Jul 1;54(7):921-6. doi: 10.1002/pbc.22367.
2
Initial testing of the aurora kinase A inhibitor MLN8237 by the Pediatric Preclinical Testing Program (PPTP).儿科临床前试验计划(PPTP)对极光激酶 A 抑制剂 MLN8237 的初步测试。
Pediatr Blood Cancer. 2010 Jul 15;55(1):26-34. doi: 10.1002/pbc.22430.
3
Safety, pharmacokinetics, and preliminary activity of the anti-IGF-1R antibody figitumumab (CP-751,871) in patients with sarcoma and Ewing's sarcoma: a phase 1 expansion cohort study.在肉瘤和尤文肉瘤患者中抗 IGF-1R 抗体 figitumumab(CP-751,871)的安全性、药代动力学和初步活性:一项 1 期扩展队列研究。
Lancet Oncol. 2010 Feb;11(2):129-35. doi: 10.1016/S1470-2045(09)70354-7. Epub 2009 Dec 23.
4
EWS/FLI and its downstream target NR0B1 interact directly to modulate transcription and oncogenesis in Ewing's sarcoma.EWS/FLI及其下游靶点NR0B1直接相互作用,以调节尤因肉瘤中的转录和肿瘤发生。
Cancer Res. 2009 Dec 1;69(23):9047-55. doi: 10.1158/0008-5472.CAN-09-1540. Epub 2009 Nov 17.
5
GSTM4 is a microsatellite-containing EWS/FLI target involved in Ewing's sarcoma oncogenesis and therapeutic resistance.GSTM4是一种含有微卫星的EWS/FLI靶点,参与尤因肉瘤的肿瘤发生和治疗抗性。
Oncogene. 2009 Nov 19;28(46):4126-32. doi: 10.1038/onc.2009.262. Epub 2009 Aug 31.
6
Analysis of Ewing sarcoma (EWS)-binding proteins: interaction with hnRNP M, U, and RNA-helicases p68/72 within protein-RNA complexes.分析尤文肉瘤(EWS)结合蛋白:与 hnRNP M、U 以及蛋白质-RNA 复合物中的 RNA 解旋酶 p68/72 的相互作用。
J Proteome Res. 2009 Oct;8(10):4455-65. doi: 10.1021/pr900235t.
7
Ewing's sarcoma origin: from duel to duality.尤因肉瘤的起源:从二元对立到二元性
Expert Rev Anticancer Ther. 2009 Aug;9(8):1025-30. doi: 10.1586/era.09.81.
8
A small molecule blocking oncogenic protein EWS-FLI1 interaction with RNA helicase A inhibits growth of Ewing's sarcoma.一种阻断致癌蛋白EWS-FLI1与RNA解旋酶A相互作用的小分子可抑制尤因肉瘤的生长。
Nat Med. 2009 Jul;15(7):750-6. doi: 10.1038/nm.1983. Epub 2009 Jul 5.
9
A molecular function map of Ewing's sarcoma.尤因肉瘤的分子功能图谱。
PLoS One. 2009;4(4):e5415. doi: 10.1371/journal.pone.0005415. Epub 2009 Apr 30.
10
An amphipathic alpha-helix controls multiple roles of brome mosaic virus protein 1a in RNA replication complex assembly and function.一个两亲性α螺旋控制着雀麦花叶病毒蛋白1a在RNA复制复合体组装和功能中的多种作用。
PLoS Pathog. 2009 Mar;5(3):e1000351. doi: 10.1371/journal.ppat.1000351. Epub 2009 Mar 27.

致癌伙伴关系:EWS-FLI1 蛋白相互作用引发尤文肉瘤的关键途径。

Oncogenic partnerships: EWS-FLI1 protein interactions initiate key pathways of Ewing's sarcoma.

机构信息

Department of Oncology and Pediatrics, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

出版信息

Clin Cancer Res. 2010 Aug 15;16(16):4077-83. doi: 10.1158/1078-0432.CCR-09-2261. Epub 2010 Jun 14.

DOI:10.1158/1078-0432.CCR-09-2261
PMID:20547696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3682924/
Abstract

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.

摘要

癌症的靶向治疗是一种黄金标准的治疗方法,它专门针对癌症,而不会对控制肿瘤以外的任何潜在部位产生影响。尤因氏肉瘤包含潜在的靶点 EWS-FLI1,这是由于一种特征性的染色体易位。EWS-FLI1 融合蛋白包含 EWS 结构域,这是一种强有力的转录激活因子,同时还包含高度保守的 FLI1 ets DNA 结合结构域。由于这些结构域的结合,EWS-FLI1 融合蛋白作为一种异常转录因子发挥作用,其表达导致细胞转化。EWS-FLI1 通过与转录和剪接中的正常细胞蛋白伴侣结合而发挥作用,类似于病毒如何利用正常细胞机制来产生病毒粒子。因此,了解 EWS-FLI1 的蛋白-蛋白相互作用以及这些伙伴关系所调控的途径,将为肿瘤发生和治疗提供信息。本综述描述了 EWS-FLI1 的已知蛋白伴侣和转录靶标,同时提出了利用靶向治疗来利用这些伙伴关系的策略。