Liver cirrhosis: molecular mechanisms and therapeutic interventions

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL MedComm Pub Date : 2024-09-17 DOI:10.1002/mco2.721
Zihe Dong, Yeying Wang, Weilin Jin
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Abstract

Liver cirrhosis is the end-stage of chronic liver disease, characterized by inflammation, necrosis, advanced fibrosis, and regenerative nodule formation. Long-term inflammation can cause continuous damage to liver tissues and hepatocytes, along with increased vascular tone and portal hypertension. Among them, fibrosis is the necessary stage and essential feature of liver cirrhosis, and effective antifibrosis strategies are commonly considered the key to treating liver cirrhosis. Although different therapeutic strategies aimed at reversing or preventing fibrosis have been developed, the effects have not be more satisfactory. In this review, we discussed abnormal changes in the liver microenvironment that contribute to the progression of liver cirrhosis and highlighted the importance of recent therapeutic strategies, including lifestyle improvement, small molecular agents, traditional Chinese medicine, stem cells, extracellular vesicles, and gut remediation, that regulate liver fibrosis and liver cirrhosis. Meanwhile, therapeutic strategies for nanoparticles are discussed, as are their possible underlying broad application and prospects for ameliorating liver cirrhosis. Finally, we also reviewed the major challenges and opportunities of nanomedicine‒biological environment interactions. We hope this review will provide insights into the pathogenesis and molecular mechanisms of liver cirrhosis, thus facilitating new methods, drug discovery, and better treatment of liver cirrhosis.

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肝硬化:分子机制和治疗干预措施
肝硬化是慢性肝病的终末阶段,以炎症、坏死、晚期纤维化和再生结节形成为特征。长期的炎症可造成肝组织和肝细胞的持续损伤,并伴有血管张力增高和门静脉高压。其中,纤维化是肝硬化的必经阶段和基本特征,有效的抗纤维化策略通常被认为是治疗肝硬化的关键。虽然旨在逆转或预防肝纤维化的治疗策略层出不穷,但效果并不尽如人意。在这篇综述中,我们讨论了导致肝硬化进展的肝脏微环境异常变化,并强调了近期治疗策略的重要性,包括改善生活方式、小分子制剂、传统中药、干细胞、细胞外囊泡和肠道修复等,这些策略可调节肝纤维化和肝硬化。同时,我们还讨论了纳米粒子的治疗策略,以及其在改善肝硬化方面可能的广泛应用和前景。最后,我们还回顾了纳米医学与生物环境相互作用的主要挑战和机遇。我们希望这篇综述能为肝硬化的发病机理和分子机制提供见解,从而促进肝硬化的新方法、新药发现和更好的治疗。
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来源期刊
CiteScore
6.70
自引率
0.00%
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0
审稿时长
10 weeks
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