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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.

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。

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