Anti-Epileptic Drug Targets Ewing Sarcoma.

Shubhalaxmi Kayarthodi, Yasuo Fujimura, Jinbo Fang, Sharif Morsalin, Veena N Rao, E Shyam P Reddy
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引用次数: 11

Abstract

Ewing Sarcoma (ES) is a rare form of bone cancer that most commonly affects children and adolescents. Chromosomal translocations are fundamental to the development of Ewing Sarcoma, linked to the changes in gene expression affecting transcription factors. Histone acetyl transferases (HATs) and histone deacetylases (HDACs) regulate transcription by modifying acetylation of both histones and transcription factors. Despite the use of multimodal therapeutic approaches current therapies are associated with significant short and long-term side effects. Hence, new therapeutic approaches are needed. In this study, we show that ERG/EWS-ERG, inhibits transcriptional activation properties of RXRα. These results suggest that ERG/EWS-ERG/EWS-Fli-1 may target transcriptional co-activators and transcriptional repressors and thereby regulate RXRα transcriptional activity. To understand the molecular mechanism of action, how the fusion protein targets nuclear receptor function, and to provide a clue for the cancer health disparity seen in Ewing Sarcoma, we hypothesized that the aberrant fusion protein, EWS-ERG/EWS-Fli-1 regulates HDACs-mediated repressor complex and inhibits the binding of transcriptional activator complex causing transcriptional repression of RXRα activity. Since it is known that HDACs regulate nuclear receptors, we proposed that HDAC inhibitor, valproic acid (VPA), an anti-epileptic drug, may reverse the inhibitory properties of EWS-ERG/EWS-Fli-1 oncoprotein on RXRα transcriptional activity and might therefore be used as therapeutic agent in ES. We demonstrate that VPA reverses the inhibitory effect of EWSERG/EWS-Fli-1 on RXRα transcriptional activity and also inhibits the cell growth. Furthermore, VPA induces apoptosis and restored the expression of RXRα target genes RARβ, CRABPII and p21 activity and repressed the expression of aberrant fusion proteins, EWS-ERG and EWS-Fli-1 in Ewing Sarcoma cells. Thus, therapeutic regulation of transcriptional repressor properties of EWS-ERG/EWS-Fli-1 with an anti-epileptic drug with a promising new potential might have a profound impact on prevention, management and treatment of Ewing Sarcoma. Therapeutic use of VPA in minority patients may help reduce the health disparity.

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抗癫痫药物靶向尤文氏肉瘤
尤文氏肉瘤(ES)是一种罕见的骨癌,最常影响儿童和青少年。染色体易位是尤文氏肉瘤发展的基础,与影响转录因子的基因表达变化有关。组蛋白乙酰转移酶(HATs)和组蛋白去乙酰化酶(hdac)通过修饰组蛋白和转录因子的乙酰化来调节转录。尽管采用了多模式治疗方法,但目前的治疗方法存在显著的短期和长期副作用。因此,需要新的治疗方法。在这项研究中,我们发现ERG/EWS-ERG抑制RXRα的转录激活特性。这些结果表明,ERG/EWS-ERG/ ews - fl -1可能靶向转录共激活因子和转录抑制因子,从而调控RXRα的转录活性。为了了解其作用的分子机制、融合蛋白如何靶向核受体功能,并为Ewing肉瘤中癌症健康差异提供线索,我们假设异常融合蛋白EWS-ERG/EWS-Fli-1调节hdac介导的抑制因子复合物并抑制转录激活因子复合物的结合,从而导致RXRα活性的转录抑制。由于已知HDAC调节核受体,我们提出HDAC抑制剂丙戊酸(VPA),一种抗癫痫药物,可能逆转EWS-ERG/ ews - fl -1癌蛋白对RXRα转录活性的抑制特性,因此可能用作ES的治疗药物。我们证明了VPA逆转了EWSERG/ ews - fl -1对RXRα转录活性的抑制作用,并抑制了细胞的生长。VPA诱导Ewing肉瘤细胞凋亡,恢复RXRα靶基因RARβ、CRABPII和p21的表达活性,抑制异常融合蛋白EWS-ERG和ews - fl -1的表达。因此,用一种具有新前景的抗癫痫药物治疗性调节EWS-ERG/ ews - fl -1的转录抑制因子特性,可能对Ewing肉瘤的预防、管理和治疗产生深远的影响。在少数患者中使用VPA治疗可能有助于减少健康差异。
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