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微小RNA作为慢性伤口愈合的治疗靶点

MicroRNA as Therapeutic Targets for Chronic Wound Healing.

作者信息

Mulholland Eoghan J, Dunne Nicholas, McCarthy Helen O

机构信息

School of Pharmacy, Queen's University of Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK.

School of Pharmacy, Queen's University of Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK; Centre for Medical Engineering Research, School of Mechanical and Manufacturing Engineering, Dublin City University, Stokes Building, Collins Avenue, Dublin 9, Ireland; Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland; Department of Mechanical and Manufacturing Engineering, School of Engineering, Trinity College Dublin, Dublin 2, Ireland.

出版信息

Mol Ther Nucleic Acids. 2017 Sep 15;8:46-55. doi: 10.1016/j.omtn.2017.06.003. Epub 2017 Jun 9.

Abstract

Wound healing is a highly complex biological process composed of three overlapping phases: inflammation, proliferation, and remodeling. Impairments at any one or more of these stages can lead to compromised healing. MicroRNAs (miRs) are non-coding RNAs that act as post-transcriptional regulators of multiple proteins and associated pathways. Thus, identification of the appropriate miR involved in the different phases of wound healing could reveal an effective third-generation genetic therapy in chronic wound care. Several miRs have been shown to be upregulated or downregulated during the wound healing process. This article examines the biological processes involved in wound healing, the miR involved at each stage, and how expression levels are modulated in the chronic wound environment. Key miRs are highlighted as possible therapeutic targets, either through underexpression or overexpression, and the healing benefits are interrogated. These are prime miR candidates that could be considered as a gene therapy option for patients suffering from chronic wounds. The success of miR as a gene therapy, however, is reliant on the development of an appropriate delivery system that must be designed to overcome both extracellular and intracellular barriers.

摘要

伤口愈合是一个高度复杂的生物学过程,由三个相互重叠的阶段组成:炎症、增殖和重塑。这些阶段中的任何一个或多个阶段出现损伤都可能导致愈合受损。微小RNA(miRs)是非编码RNA,可作为多种蛋白质和相关信号通路的转录后调节因子。因此,确定参与伤口愈合不同阶段的合适miR,可能会揭示一种用于慢性伤口护理的有效的第三代基因疗法。在伤口愈合过程中,已有几种miR被证明上调或下调。本文探讨了伤口愈合所涉及的生物学过程、每个阶段涉及的miR,以及在慢性伤口环境中表达水平是如何被调节的。重点介绍了关键miR作为可能的治疗靶点,通过低表达或过表达来探究其愈合益处。这些是主要的miR候选物,可被视为慢性伤口患者基因治疗的一种选择。然而,miR作为基因疗法的成功依赖于开发一种合适的递送系统,该系统必须设计成能够克服细胞外和细胞内的障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aef/5485763/6969b9c6a0c6/fx1.jpg

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