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

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Cristian Ichim, Adrian Boicean, Paula Anderco, Samuel Bogdan Todor, Adrian Hașegan, Sabrina Bîrsan, Victoria Bîrluțiu
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引用次数: 0

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.

Abstract Image

肝硬化中的microrna:诊断和治疗的观点-一个全面的综述。
肝硬化是慢性肝损伤的终末期,由多种病因引起,包括病毒性肝炎、酒精滥用和非酒精性脂肪肝。肝硬化的一个关键驱动因素是肝纤维化,这是一个涉及肝星状细胞活化、炎症信号和细胞外基质积累的多方面过程。MicroRNAs (miRNAs)是一类小的非编码rna,在这方面已经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mirna在肝硬化中作用的现有证据,重点介绍了miR-21、miR-122、miR-125、miR-146和miR-155等特异性mirna。这些mirna影响TGF-β、NF-κB和PI3K/Akt信号通路,促进纤维化进程或抑制纤维化进程。mirna在生物体液中独特的表达谱和稳定性使其成为肝硬化诊断和监测的有前途的非侵入性生物标志物。此外,通过模拟物或抑制剂进行miRNA活性的治疗性调节具有未来的潜力,尽管递送和安全性方面的挑战仍然存在。推进我们对肝硬化中mirna介导的调控的理解可以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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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