miR-21是心血管疾病的治疗靶点吗?

Antoinette Holland, Molly Enrick, Arianna Diaz, Liya Yin
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引用次数: 1

摘要

微小RNA-21(miR-21)通过调节信使RNA在分子水平上发挥多种功能。先前的研究激发了人们对miR-21作为心血管疾病潜在治疗靶点的作用的兴趣。miR-21的表达有助于许多细胞类型的分化、增殖和成熟,如成纤维细胞、内皮细胞、心肌细胞和内皮祖细胞。miR-21的功能取决于其在特定细胞类型和下游靶点中的表达水平,这些靶点决定了细胞的命运。在病理条件下,miR-21的表达水平发生改变,导致下游信号传导和心血管疾病的异常基因调节,如高血压、心肌肥大和纤维化、动脉粥样硬化和心力衰竭。可以将激动剂或抗酸剂引入相应的组织类型中,以逆转或阻止疾病的进展。细胞外囊泡中的外泌体以高生物相容性介导许多细胞事件,具有将miR-21有效递送到靶细胞的高潜力。miR-21在心血管疾病(CVD)中的关键作用是无可争议的,但关于miR-21在同一疾病中的功能,有争议的报道。这种差异激发了人们对更好地理解miR-21在各种疾病不同阶段的不同组织中的作用以及miR-21抑制剂如何发挥作用的兴趣。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is miR-21 A Therapeutic Target in Cardiovascular Disease?

microRNA-21 (miR-21) serves a multitude of functions at the molecular level through its regulation of messenger RNA. Previous research has sparked interest in the role of miR-21 as a potential therapeutic target in cardiovascular diseases. miR-21 expression contributes to the differentiation, proliferation, and maturation of many cell types, such as fibroblasts, endothelial cells, cardiomyocytes, and endothelial progenitor cells. The function of miR-21 depends upon its expression level in the specific cell types and downstream targets, which determine cell fate. Under pathological conditions, the expression level of miR-21 is altered, leading to abnormal gene regulation of downstream signaling and cardiovascular diseases such as hypertension, cardiac hypertrophy and fibrosis, atherosclerosis, and heart failure. Agomirs or antagomirs can be introduced into the respective tissue type to reverse or stop the progression of the disease. Exosomes in the extracellular vesicles, which mediate many cellular events with high biocompatibility, have a high potential of efficiently delivering miR-21 to their targeted cells. The critical role of miR-21 in cardiovascular disease (CVD) is indisputable, but there are controversial reports on the function of miR-21 in the same disease. This discrepancy sparks interest in better understanding the role of miR-21 in different tissues under different stages of various diseases and the mechanism of how miR-21 inhibitors work.

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