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靶向长链非编码 RNA 以治疗性地上调基因表达。

Targeting long non-coding RNA to therapeutically upregulate gene expression.

机构信息

Center for Therapeutic Innovation and the Department of Psychiatry and Behavioral Sciences, University of Miami Miller School of Medicine, 1501 NW 10th Avenue, Miami 33136, Florida, USA.

出版信息

Nat Rev Drug Discov. 2013 Jun;12(6):433-46. doi: 10.1038/nrd4018.

Abstract

The majority of currently available drugs and tool compounds exhibit an inhibitory mechanism of action and there is a relative lack of pharmaceutical agents that are capable of increasing the activity of effectors or pathways for therapeutic benefit. Indeed, the upregulation of many genes, including tumour suppressors, growth factors, transcription factors and genes that are deficient in various genetic diseases, would be desired in specific situations. Recently, key roles for regulatory long non-coding RNAs (lncRNAs) in the regulation of gene expression have begun to emerge. lncRNAs can positively or negatively regulate gene expression and chromatin architecture. Here, we review the current understanding of the mechanisms of action of lncRNAs and their roles in disease, focusing on recent work in the design of inhibitors of the natural antisense transcript (NAT) class of lncRNAs, known as antagoNAT oligonucleotides, and the issues associated with their potential therapeutic application.

摘要

目前大多数可用的药物和工具化合物都表现出抑制作用机制,而能够增加效应器或途径活性以产生治疗益处的药物相对较少。实际上,在某些特定情况下,人们希望上调许多基因的活性,包括肿瘤抑制因子、生长因子、转录因子和各种遗传疾病中缺失的基因。最近,调控长非编码 RNA(lncRNA)在基因表达调控中的关键作用开始显现。lncRNA 可以正向或负向调控基因表达和染色质结构。在这里,我们综述了 lncRNA 的作用机制及其在疾病中的作用的最新认识,重点介绍了天然反义转录本(NAT)类 lncRNA 抑制剂的设计,即反义核苷酸,以及与它们潜在治疗应用相关的问题。

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