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基于小核酸的治疗策略,靶向调控动脉粥样硬化中血管炎症、重塑和纤维化的转录因子。

Small-nucleic-acid-based therapeutic strategy targeting the transcription factors regulating the vascular inflammation, remodeling and fibrosis in atherosclerosis.

作者信息

Youn Sung Won, Park Kwan-Kyu

机构信息

Department of Radiology, Catholic University of Daegu Medical Center, School of Medicine, Catholic University of Daegu, Daegu 705-718, Korea.

Department of Pathology, Catholic University of Daegu Medical Center, School of Medicine, Catholic University of Daegu, Daegu 705-718, Korea.

出版信息

Int J Mol Sci. 2015 May 22;16(5):11804-33. doi: 10.3390/ijms160511804.

Abstract

Atherosclerosis arises when injury to the arterial wall induces an inflammatory cascade that is sustained by a complex network of cytokines, together with accumulation of lipids and fibrous material. Inflammatory cascades involve leukocyte adherence and chemotaxis, which are coordinated by the local secretion of adhesion molecules, chemotactic factors, and cytokines. Transcription factors are critical to the integration of the various steps of the cascade response to mediators of vascular injury, and are induced in a stimulus-dependent and cell-type-specific manner. Several small-nucleic-acid-based therapeutic strategies have recently been developed to target transcription factors: antisense oligodeoxynucleotides, RNA interference, microRNA, and decoy oligodeoxynucleotides. The aim of this review was to provide an overview of these particular targeted therapeutic strategies, toward regulation of the vascular inflammation, remodeling and fibrosis associated with atherosclerosis.

摘要

当动脉壁损伤引发炎症级联反应时,动脉粥样硬化就会出现,这种炎症级联反应由细胞因子的复杂网络维持,并伴有脂质和纤维物质的积累。炎症级联反应涉及白细胞黏附和趋化作用,这是由黏附分子、趋化因子和细胞因子的局部分泌协调的。转录因子对于对血管损伤介质的级联反应的各个步骤的整合至关重要,并以刺激依赖和细胞类型特异性的方式被诱导。最近已经开发了几种基于小核酸的治疗策略来靶向转录因子:反义寡脱氧核苷酸、RNA干扰、微小RNA和诱饵寡脱氧核苷酸。这篇综述的目的是概述这些特定的靶向治疗策略,以调节与动脉粥样硬化相关的血管炎症、重塑和纤维化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a6a/4463731/00c76d397bd4/ijms-16-11804-g001.jpg

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