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首页> 外文期刊>Trends in molecular medicine >G-quadruplex, Friend or Foe: The Role of the G-quartet in Anticancer Strategies
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G-quadruplex, Friend or Foe: The Role of the G-quartet in Anticancer Strategies

机译:g-quadruplex,friend或foe:g-quartet在抗癌策略中的作用

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摘要

The clinical applicability of G-quadruplexes (G4s) as anticancer drugs is currently being evaluated. Several G4 ligands and aptamers are undergoing clinical trials following the notable examples of quarfloxin and AS1411, respectively. In this review, we summarize the latest achievements and breakthroughs in the use of G4 nucleic acids as both therapeutic tools ('friends', as healing anticancer drugs) and targets ('foes', within the harmful cancer cell), particularly using aptamers and quadruplex-targeted ligands, respectively. We explore the recent research on synthetic G4 ligands toward the discovery of anticancer therapeutics and their mechanism of action. Additionally, we highlight recent advances in chemical and structural biology that enable the design of specific G4 aptamers to be used as novel anticancer agents.
机译:目前正在评估G-四链体(G4s)作为抗癌药物的临床适用性。在quarfloxin和AS1411的显著例子之后,一些G4配体和适体正在进行临床试验。在这篇综述中,我们总结了G4核酸作为治疗工具(“朋友”,作为治疗抗癌药物)和靶点(“敌人”,在有害癌细胞内)的最新成就和突破,特别是分别使用适体和四联靶向配体。我们探讨了合成G4配体的最新研究,以发现抗癌疗法及其作用机制。此外,我们还重点介绍了化学和结构生物学方面的最新进展,这些进展使特定G4适体的设计能够用作新型抗癌剂。

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  • 来源
    《Trends in molecular medicine》 |2020年第9期|共14页
  • 作者单位

    Univ Beira Interior CICS UBI Ctr Invest Ciencias Saude Ave Infante D Henrique P-6200506 Covilha;

    Univ Bordeaux ARNA Lab INSERM U1212 CNRS UMR 5320 IECB F-33600 Pessac France;

    Univ Bordeaux ARNA Lab INSERM U1212 CNRS UMR 5320 IECB F-33600 Pessac France;

    Univ Beira Interior CICS UBI Ctr Invest Ciencias Saude Ave Infante D Henrique P-6200506 Covilha;

    Univ Beira Interior CICS UBI Ctr Invest Ciencias Saude Ave Infante D Henrique P-6200506 Covilha;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

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