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Advancements in MAFLD Modeling with Human Cell and Organoid Models

Metabolic (dysfunction) associated fatty liver disease (MAFLD) is one of the most prevalent liver diseases and has no approved therapeutics. The high failure rates witnessed in late-phase MAFLD drug trials reflect the complexity of the disease, and how the disease develops and progresses remains to...

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Autores principales: Wang, Shi-Xiang, Yan, Ji-Song, Chan, Yun-Shen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569457/
https://www.ncbi.nlm.nih.gov/pubmed/36233151
http://dx.doi.org/10.3390/ijms231911850
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author Wang, Shi-Xiang
Yan, Ji-Song
Chan, Yun-Shen
author_facet Wang, Shi-Xiang
Yan, Ji-Song
Chan, Yun-Shen
author_sort Wang, Shi-Xiang
collection PubMed
description Metabolic (dysfunction) associated fatty liver disease (MAFLD) is one of the most prevalent liver diseases and has no approved therapeutics. The high failure rates witnessed in late-phase MAFLD drug trials reflect the complexity of the disease, and how the disease develops and progresses remains to be fully understood. In vitro, human disease models play a pivotal role in mechanistic studies to unravel novel disease drivers and in drug testing studies to evaluate human-specific responses. This review focuses on MAFLD disease modeling using human cell and organoid models. The spectrum of patient-derived primary cells and immortalized cell lines employed to model various liver parenchymal and non-parenchymal cell types essential for MAFLD development and progression is discussed. Diverse forms of cell culture platforms utilized to recapitulate tissue-level pathophysiology in different stages of the disease are also reviewed.
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spelling pubmed-95694572022-10-17 Advancements in MAFLD Modeling with Human Cell and Organoid Models Wang, Shi-Xiang Yan, Ji-Song Chan, Yun-Shen Int J Mol Sci Review Metabolic (dysfunction) associated fatty liver disease (MAFLD) is one of the most prevalent liver diseases and has no approved therapeutics. The high failure rates witnessed in late-phase MAFLD drug trials reflect the complexity of the disease, and how the disease develops and progresses remains to be fully understood. In vitro, human disease models play a pivotal role in mechanistic studies to unravel novel disease drivers and in drug testing studies to evaluate human-specific responses. This review focuses on MAFLD disease modeling using human cell and organoid models. The spectrum of patient-derived primary cells and immortalized cell lines employed to model various liver parenchymal and non-parenchymal cell types essential for MAFLD development and progression is discussed. Diverse forms of cell culture platforms utilized to recapitulate tissue-level pathophysiology in different stages of the disease are also reviewed. MDPI 2022-10-06 /pmc/articles/PMC9569457/ /pubmed/36233151 http://dx.doi.org/10.3390/ijms231911850 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Shi-Xiang
Yan, Ji-Song
Chan, Yun-Shen
Advancements in MAFLD Modeling with Human Cell and Organoid Models
title Advancements in MAFLD Modeling with Human Cell and Organoid Models
title_full Advancements in MAFLD Modeling with Human Cell and Organoid Models
title_fullStr Advancements in MAFLD Modeling with Human Cell and Organoid Models
title_full_unstemmed Advancements in MAFLD Modeling with Human Cell and Organoid Models
title_short Advancements in MAFLD Modeling with Human Cell and Organoid Models
title_sort advancements in mafld modeling with human cell and organoid models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9569457/
https://www.ncbi.nlm.nih.gov/pubmed/36233151
http://dx.doi.org/10.3390/ijms231911850
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