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肝硬化中的微小RNA:诊断与治疗前景——一篇综述

MicroRNAs in Liver Cirrhosis: Diagnostic and Therapeutic Perspectives-A Comprehensive Review.

作者信息

Ichim Cristian, Boicean Adrian, Anderco Paula, Todor Samuel Bogdan, Hașegan Adrian, Bîrsan Sabrina, Bîrluțiu Victoria

机构信息

Faculty of Medicine, Lucian Blaga University of Sibiu, 550024 Sibiu, Romania.

出版信息

J Pers Med. 2025 Aug 14;15(8):376. doi: 10.3390/jpm15080376.

Abstract

Liver cirrhosis represents the end-stage of chronic hepatic injury, arising from a diverse range of etiologies including viral hepatitis, alcohol abuse and non-alcoholic fatty liver disease. A key driver of cirrhosis is hepatic fibrogenesis, a multifaceted process involving hepatic stellate cell activation, inflammatory signaling and extracellular matrix accumulation. MicroRNAs (miRNAs), a class of small non-coding RNAs, have emerged as pivotal regulators in this context, modulating gene expression networks that govern inflammation, fibrosis and hepatocarcinogenesis. This review synthesizes current evidence on the role of miRNAs in liver cirrhosis, emphasizing specific miRNAs such as miR-21, miR-122, miR-125, miR-146 and miR-155. These miRNAs influence pathways involving TGF-β, NF-κB and PI3K/Akt signaling, contributing to either fibrogenic progression or its suppression. The unique expression profiles and stability of miRNAs in biological fluids position them as promising non-invasive biomarkers for cirrhosis diagnosis and monitoring. Moreover, therapeutic modulation of miRNA activity through mimics or inhibitors holds future potential, though delivery and safety challenges remain. Advancing our understanding of miRNA-mediated regulation in cirrhosis could transform current diagnostic and therapeutic strategies, enabling more precise and personalized liver disease management.

摘要

肝硬化代表慢性肝损伤的终末期,其病因多种多样,包括病毒性肝炎、酒精滥用和非酒精性脂肪性肝病。肝硬化的一个关键驱动因素是肝纤维化,这是一个多方面的过程,涉及肝星状细胞激活、炎症信号传导和细胞外基质积累。微小RNA(miRNA)是一类小的非编码RNA,在这种情况下已成为关键的调节因子,调节控制炎症、纤维化和肝癌发生的基因表达网络。本综述综合了目前关于miRNA在肝硬化中作用的证据,重点介绍了特定的miRNA,如miR-21、miR-122、miR-125、miR-146和miR-155。这些miRNA影响涉及转化生长因子-β(TGF-β)、核因子-κB(NF-κB)和磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)信号传导的途径,促进纤维化进展或抑制纤维化。miRNA在生物体液中的独特表达谱和稳定性使其成为肝硬化诊断和监测有前景的非侵入性生物标志物。此外,通过模拟物或抑制剂对miRNA活性进行治疗性调节具有未来潜力,尽管递送和安全性挑战仍然存在。加深我们对肝硬化中miRNA介导的调节的理解可能会改变当前的诊断和治疗策略,实现更精确和个性化的肝病管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95e4/12387485/626ba91599e3/jpm-15-00376-g001.jpg

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