翻译中的治疗机会

J. Pelletier, S. Peltz
{"title":"翻译中的治疗机会","authors":"J. Pelletier, S. Peltz","doi":"10.1101/087969767.48.855","DOIUrl":null,"url":null,"abstract":"The protein synthesis apparatus and signaling pathways that regulate its activity represent excellent, largely unexploited targets for small-molecule discovery. Approaches that disrupt this process can cause either qualitative or quantitative changes in mRNA expression. Interference with the function of rRNA, tRNA, or general protein factors is likely to exert effects on global protein synthesis. On the other hand, compounds that target the ribosome recruitment phase of translation have the potential to selectively inhibit gene expression. A significant portion of our current understanding of the translation process is a consequence of utilizing small molecules to chemically dissect this complex process (Pestka 1977; Vazquez 1979). Such probes have been used to perturb the translation process in vitro and in vivo, freeze short-lived intermediates that otherwise could not be studied, identify new initiation factors, and therapeutically target this process in pathogenic organisms. At a time when novel approaches for discovering new drugs to treat a range of microbial, viral, and metabolic diseases are sought, it would seem opportune to review our understanding of small molecules that target translation. Herein, we discuss various aspects of the translation process that have recently been explored as targets for small-molecule discovery. The potential for targeting this process as an anticancer approach is also addressed. Finally, we review examples of small-molecule inhibitors of translation that are clinically used as anti-infective agents. SMALL-MOLECULE APPROACHES THAT QUALITATIVELY ALTER MRNA TRANSLATION Treating Genetic Disorders by Promoting Readthrough of Nonsense Mutations Genetic disorders often arise as a consequence of mutations that abolish...","PeriodicalId":10493,"journal":{"name":"Cold Spring Harbor Monograph Archive","volume":"100 1","pages":"855-895"},"PeriodicalIF":0.0000,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"17","resultStr":"{\"title\":\"30 Therapeutic Opportunities in Translation\",\"authors\":\"J. Pelletier, S. Peltz\",\"doi\":\"10.1101/087969767.48.855\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The protein synthesis apparatus and signaling pathways that regulate its activity represent excellent, largely unexploited targets for small-molecule discovery. Approaches that disrupt this process can cause either qualitative or quantitative changes in mRNA expression. Interference with the function of rRNA, tRNA, or general protein factors is likely to exert effects on global protein synthesis. On the other hand, compounds that target the ribosome recruitment phase of translation have the potential to selectively inhibit gene expression. A significant portion of our current understanding of the translation process is a consequence of utilizing small molecules to chemically dissect this complex process (Pestka 1977; Vazquez 1979). Such probes have been used to perturb the translation process in vitro and in vivo, freeze short-lived intermediates that otherwise could not be studied, identify new initiation factors, and therapeutically target this process in pathogenic organisms. At a time when novel approaches for discovering new drugs to treat a range of microbial, viral, and metabolic diseases are sought, it would seem opportune to review our understanding of small molecules that target translation. Herein, we discuss various aspects of the translation process that have recently been explored as targets for small-molecule discovery. The potential for targeting this process as an anticancer approach is also addressed. Finally, we review examples of small-molecule inhibitors of translation that are clinically used as anti-infective agents. SMALL-MOLECULE APPROACHES THAT QUALITATIVELY ALTER MRNA TRANSLATION Treating Genetic Disorders by Promoting Readthrough of Nonsense Mutations Genetic disorders often arise as a consequence of mutations that abolish...\",\"PeriodicalId\":10493,\"journal\":{\"name\":\"Cold Spring Harbor Monograph Archive\",\"volume\":\"100 1\",\"pages\":\"855-895\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"17\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cold Spring Harbor Monograph Archive\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/087969767.48.855\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cold Spring Harbor Monograph Archive","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/087969767.48.855","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 17

摘要

蛋白质合成装置和调节其活性的信号通路为小分子发现提供了极好的、很大程度上尚未开发的靶点。破坏这一过程的方法可以导致mRNA表达的定性或定量变化。干扰rRNA、tRNA或一般蛋白质因子的功能可能会对整体蛋白质合成产生影响。另一方面,靶向翻译的核糖体募集阶段的化合物具有选择性抑制基因表达的潜力。我们目前对翻译过程的理解的一个重要部分是利用小分子化学解剖这个复杂过程的结果(Pestka 1977;巴斯克斯1979)。这些探针已被用于干扰体外和体内的翻译过程,冻结否则无法研究的短寿命中间体,识别新的起始因子,并在致病生物中治疗靶向这一过程。在寻找新方法来发现治疗一系列微生物、病毒和代谢疾病的新药物的时候,似乎是时候回顾我们对靶向翻译的小分子的理解了。在这里,我们讨论了翻译过程的各个方面,这些方面最近被探索作为小分子发现的目标。本文还讨论了靶向这一过程作为抗癌方法的潜力。最后,我们回顾了临床上用作抗感染药物的小分子翻译抑制剂的例子。通过促进无义突变的读通来定性地改变MRNA翻译的小分子方法治疗遗传疾病遗传疾病通常是由于消除…
本文章由计算机程序翻译,如有差异,请以英文原文为准。
30 Therapeutic Opportunities in Translation
The protein synthesis apparatus and signaling pathways that regulate its activity represent excellent, largely unexploited targets for small-molecule discovery. Approaches that disrupt this process can cause either qualitative or quantitative changes in mRNA expression. Interference with the function of rRNA, tRNA, or general protein factors is likely to exert effects on global protein synthesis. On the other hand, compounds that target the ribosome recruitment phase of translation have the potential to selectively inhibit gene expression. A significant portion of our current understanding of the translation process is a consequence of utilizing small molecules to chemically dissect this complex process (Pestka 1977; Vazquez 1979). Such probes have been used to perturb the translation process in vitro and in vivo, freeze short-lived intermediates that otherwise could not be studied, identify new initiation factors, and therapeutically target this process in pathogenic organisms. At a time when novel approaches for discovering new drugs to treat a range of microbial, viral, and metabolic diseases are sought, it would seem opportune to review our understanding of small molecules that target translation. Herein, we discuss various aspects of the translation process that have recently been explored as targets for small-molecule discovery. The potential for targeting this process as an anticancer approach is also addressed. Finally, we review examples of small-molecule inhibitors of translation that are clinically used as anti-infective agents. SMALL-MOLECULE APPROACHES THAT QUALITATIVELY ALTER MRNA TRANSLATION Treating Genetic Disorders by Promoting Readthrough of Nonsense Mutations Genetic disorders often arise as a consequence of mutations that abolish...
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信