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Autores principales: Zihe Dong, Yeying Wang, Weilin Jin
Formato: Artículo Open Access
Publicado: Wiley 2024
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Acceso en línea:https://onlinelibrary.wiley.com/doi/10.1002/mco2.721
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author Zihe Dong
Yeying Wang
Weilin Jin
author_facet Zihe Dong
Yeying Wang
Weilin Jin
Zihe Dong
Yeying Wang
Weilin Jin
collection Wiley Open Access
contents Liver cirrhosis: molecular mechanisms and therapeutic interventions Zihe Dong Yeying Wang Weilin Jin MedComm AbstractLiver 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. 10.1002/mco2.721 http://creativecommons.org/licenses/by/4.0/
doi_str_mv 10.1002/mco2.721
format Artículo Open Access
id wiley_oa_10_1002_mco2_721
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by/4.0/
publishDate 2024
publisher Wiley
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spellingShingle Liver cirrhosis: molecular mechanisms and therapeutic interventions
Zihe Dong
Yeying Wang
Weilin Jin
MedComm
Liver cirrhosis: molecular mechanisms and therapeutic interventions Zihe Dong Yeying Wang Weilin Jin MedComm AbstractLiver 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. 10.1002/mco2.721 http://creativecommons.org/licenses/by/4.0/
title Liver cirrhosis: molecular mechanisms and therapeutic interventions
topic MedComm
url https://onlinelibrary.wiley.com/doi/10.1002/mco2.721