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抗癫痫药物靶向尤因肉瘤。

Anti-Epileptic Drug Targets Ewing Sarcoma.

作者信息

Kayarthodi Shubhalaxmi, Fujimura Yasuo, Fang Jinbo, Morsalin Sharif, Rao Veena N, Reddy E Shyam P

机构信息

Cancer Biology Program, Department of OB/GYN, Morehouse School of Medicine, Georgia Cancer Center for Excellence, Grady Memorial Hospital, 80 Jesse Hill Jr. Drive, Atlanta, 30303, GA.

出版信息

J Pharm Sci Pharmacol. 2014 Jun 1;1(2):87-100. doi: 10.1166/jpsp.2014.1013.

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 RXR. These results suggest that ERG/EWS-ERG/EWS-Fli-1 may target transcriptional co-activators and transcriptional repressors and thereby regulate RXR 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 RXR 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 RXR 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 RXR transcriptional activity and also inhibits the cell growth. Furthermore, VPA induces apoptosis and restored the expression of RXR target genes RAR, 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.

摘要

尤因肉瘤(ES)是一种罕见的骨癌形式,最常影响儿童和青少年。染色体易位是尤因肉瘤发展的基础,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(HDACs)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,但目前的治疗仍伴有显著的短期和长期副作用。因此,需要新的治疗方法。在本研究中,我们表明ERG/EWS-ERG抑制RXR的转录激活特性。这些结果表明,ERG/EWS-ERG/EWS-Fli-1可能靶向转录共激活因子和转录抑制因子,从而调节RXR的转录活性。为了了解其分子作用机制、融合蛋白如何靶向核受体功能,并为尤因肉瘤中观察到的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HDACs介导的抑制复合物,并抑制转录激活复合物的结合,从而导致RXR活性的转录抑制。由于已知HDACs调节核受体,我们提出HDAC抑制剂丙戊酸(VPA),一种抗癫痫药物,可能会逆转EWS-ERG/EWS-Fli-1癌蛋白对RXR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VPA可逆转EWSERG/EWS-Fli-1对RXR转录活性的抑制作用,并抑制细胞生长。此外,VPA诱导凋亡并恢复RXR靶基因RAR、CRABPII和p21的活性表达,并抑制尤因肉瘤细胞中异常融合蛋白EWS-ERG和EWS-Fli-1的表达。因此,用具有潜在前景的抗癫痫药物对EWS-ERG/EWS-Fli-1的转录抑制特性进行治疗性调节,可能会对尤因肉瘤的预防、管理和治疗产生深远影响。在少数族裔患者中使用VPA进行治疗可能有助于减少健康差异。

相似文献

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Anti-Epileptic Drug Targets Ewing Sarcoma.抗癫痫药物靶向尤因肉瘤。
J Pharm Sci Pharmacol. 2014 Jun 1;1(2):87-100. doi: 10.1166/jpsp.2014.1013.

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Sodium valproate: an old drug with new roles.丙戊酸钠:一种有新作用的老药。
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