• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

药物评估:PTC-124——一种治疗囊性纤维化和杜氏肌营养不良症的潜在药物。

Drug evaluation: PTC-124--a potential treatment of cystic fibrosis and Duchenne muscular dystrophy.

作者信息

Hamed Sherifa A

机构信息

Saudi German Hospital - Aseer, PO Box 2553, Khamis Mushayt 61961, Saudi Arabia.

出版信息

IDrugs. 2006 Nov;9(11):783-9.

PMID:17096300
Abstract

PTC-124, a 1,2,4-oxadiazole compound, is in development by PTC Therapeutics Inc as an orally active small molecule that can override nonsense stop translation signals to produce full-length proteins. PTC-124 is currently being evaluated in phase II clinical trials against cystic fibrosis (CF) and Duchenne muscular dystrophy (DMD). The functional properties of PTC-124 are similar to the aminoglycoside antibiotic gentamicin, but the two compounds are chemically distinct and PTC-124 does not exhibit any antibiotic characteristics. In vitro experiments showed PTC-124 to be superior to gentamicin at ribosomal read-through of nonsense mutations. In vivo investigations revealed that PTC-124 was effective in restoring the production of full-length protein in animal models of CF and DMD. Phase I clinical trials reported that PTC-124 was well tolerated in healthy patients. The author concludes that the encouraging results observed to date make PTC-124 an attractive option for further well-designed, long-term human studies on larger sample populations. The author also predicts that if results continue to be positive, PTC-124 could also be trialed in other single gene disorders with nonsense mutations such as hemophilia, neurofibromatosis, retinitis pigmentosa, bullous skin diseases and lysosomal storage disorders.

摘要

PTC-124是一种1,2,4-恶二唑化合物,由PTC治疗公司研发,是一种口服活性小分子,它能够绕过无义终止翻译信号来产生全长蛋白质。PTC-124目前正在针对囊性纤维化(CF)和杜氏肌营养不良症(DMD)进行II期临床试验评估。PTC-124的功能特性与氨基糖苷类抗生素庆大霉素相似,但这两种化合物在化学结构上不同,且PTC-124不具有任何抗生素特性。体外实验表明,在无义突变的核糖体通读方面,PTC-124优于庆大霉素。体内研究显示,PTC-124在CF和DMD动物模型中能有效恢复全长蛋白质的产生。I期临床试验报告称,PTC-124在健康患者中耐受性良好。作者得出结论,迄今为止观察到的令人鼓舞的结果使PTC-124成为进一步针对更大样本群体进行精心设计的长期人体研究的一个有吸引力的选择。作者还预测,如果结果继续呈阳性,PTC-124也可用于其他具有无义突变的单基因疾病的试验,如血友病、神经纤维瘤病、视网膜色素变性、大疱性皮肤病和溶酶体贮积症。

相似文献

1
Drug evaluation: PTC-124--a potential treatment of cystic fibrosis and Duchenne muscular dystrophy.药物评估:PTC-124——一种治疗囊性纤维化和杜氏肌营养不良症的潜在药物。
IDrugs. 2006 Nov;9(11):783-9.
2
A novel approach to identify Duchenne muscular dystrophy patients for aminoglycoside antibiotics therapy.一种识别杜氏肌营养不良症患者以进行氨基糖苷类抗生素治疗的新方法。
Brain Dev. 2005 Sep;27(6):400-5. doi: 10.1016/j.braindev.2004.09.014. Epub 2004 Dec 8.
3
Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations.庆大霉素治疗由无义突变引起的杜兴氏和贝克氏肌肉营养不良症。
Ann Neurol. 2001 Jun;49(6):706-11.
4
Molecule of the month. Ataluren.本月分子。阿他芦胺。
Drug News Perspect. 2010 Mar;23(2):135.
5
Reading through premature stop codons with PTC1 24. Project Catalyst to find more Duchenne drugs. Interview by Guenter Scheuerbrandt.
Acta Myol. 2008 Oct;27:63-8.
6
Safety, tolerability, and pharmacokinetics of PTC124, a nonaminoglycoside nonsense mutation suppressor, following single- and multiple-dose administration to healthy male and female adult volunteers.非氨基糖苷类无义突变抑制剂PTC124在健康成年男性和女性志愿者单剂量及多剂量给药后的安全性、耐受性和药代动力学。
J Clin Pharmacol. 2007 Apr;47(4):430-44. doi: 10.1177/0091270006297140.
7
Pharmaceutical therapies to recode nonsense mutations in inherited diseases.用于重编码遗传性疾病无义突变的药物治疗方法。
Pharmacol Ther. 2012 Nov;136(2):227-66. doi: 10.1016/j.pharmthera.2012.07.007. Epub 2012 Jul 20.
8
Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy.氨基糖苷类诱导的终止密码子通读的序列特异性:对杜氏肌营养不良症治疗的潜在意义。
Ann Neurol. 2000 Aug;48(2):164-9.
9
Ataluren: first global approval.依伐鲁肽:全球首次获批。
Drugs. 2014 Sep;74(14):1709-14. doi: 10.1007/s40265-014-0287-4.
10
Introducing sense into nonsense in treatments of human genetic diseases.在人类遗传疾病治疗中化无意义为有意义。
Trends Genet. 2008 Nov;24(11):552-63. doi: 10.1016/j.tig.2008.08.010. Epub 2008 Oct 18.

引用本文的文献

1
Advanced genetic therapies for the treatment of Rett syndrome: state of the art and future perspectives.用于治疗雷特综合征的先进基因疗法:现状与未来展望。
Front Neurosci. 2023 May 25;17:1172805. doi: 10.3389/fnins.2023.1172805. eCollection 2023.
2
Read-through approach for stop mutations in Duchenne muscular dystrophy. An update.通读方法治疗杜氏肌营养不良症中的终止突变。更新。
Acta Myol. 2021 Mar 31;40(1):43-50. doi: 10.36185/2532-1900-041. eCollection 2021 Mar.
3
Gene therapy for haemophilia.血友病的基因治疗。
Cochrane Database Syst Rev. 2020 Apr 28;4(4):CD010822. doi: 10.1002/14651858.CD010822.pub4.
4
Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.囊性纤维化中的囊性纤维化跨膜传导调节因子调节剂:当前观点
Clin Pharmacol. 2016 Sep 21;8:127-140. doi: 10.2147/CPAA.S100759. eCollection 2016.
5
CFTR Modulators for the Treatment of Cystic Fibrosis.用于治疗囊性纤维化的CFTR调节剂
P T. 2014 Jul;39(7):500-11.
6
Molecular and cell-based therapies for muscle degenerations: a road under construction.用于肌肉退化的分子和细胞疗法:正在建设中的道路。
Front Physiol. 2014 Apr 8;5:119. doi: 10.3389/fphys.2014.00119. eCollection 2014.
7
Novel compounds for the treatment of Duchenne muscular dystrophy: emerging therapeutic agents.用于治疗杜氏肌营养不良症的新型化合物:新兴治疗药物。
Appl Clin Genet. 2011 Mar 10;4:29-44. doi: 10.2147/TACG.S8762. Print 2011.
8
SMRT compounds correct nonsense mutations in primary immunodeficiency and other genetic models.SMRT 化合物可纠正原发性免疫缺陷和其他遗传模型中的无义突变。
Ann N Y Acad Sci. 2012 Feb;1250:33-40. doi: 10.1111/j.1749-6632.2012.06467.x.
9
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.通过直接测序检测到肌营养不良蛋白基因的新型核苷酸改变的患者队列的临床和分子特征。
BMC Med Genet. 2011 Mar 11;12:37. doi: 10.1186/1471-2350-12-37.
10
Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy.氨基糖苷类诱导的突变抑制(终止密码子通读)作为杜氏肌营养不良症的一种治疗策略。
Ther Adv Neurol Disord. 2010 Nov;3(6):379-89. doi: 10.1177/1756285610388693.