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Lipotoxicity-driven metabolic dysfunction-associated steatotic liver disease (MASLD).

Authors :
Iturbe-Rey S
Maccali C
Arrese M
Aspichueta P
Oliveira CP
Castro RE
Lapitz A
Izquierdo-Sanchez L
Bujanda L
Perugorria MJ
Banales JM
Rodrigues PM
Source :
Atherosclerosis [Atherosclerosis] 2024 Nov 14; Vol. 400, pp. 119053. Date of Electronic Publication: 2024 Nov 14.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) encompasses a spectrum of liver lesions, ranging from simple steatosis to metabolic dysfunction-associated steatohepatitis (MASH), that may further progress to cirrhosis. MASLD is estimated to affect more than one third of the general population and it represents a risk factor for end-stage liver failure and liver cancer, substantially contributing to liver-related morbidity and mortality. Although the pathogenesis of MASLD is incompletely understood, it is known to consist of a multifactorial process influenced by extrinsic and intrinsic factors such as metabolic, environmental and demographic features, gut microbiota and genetics. Dysregulation of both extracellular and intracellular lipid composition is known to promote the generation of toxic lipid species, thereby triggering lipotoxicity and cellular stress. These events ultimately lead to the activation of distinct cell death pathways, resulting in inflammation, fibrogenesis and, eventually, carcinogenesis. In this manuscript, we provide a comprehensive review of the role of lipotoxicity during MASLD pathogenesis, discussing the most relevant lipid species and related molecular mechanisms, summarizing the cell type-specific effects and highlighting the most promising putative therapeutic strategies for modulating lipotoxicity and lipid metabolism in MASLD.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1879-1484
Volume :
400
Database :
MEDLINE
Journal :
Atherosclerosis
Publication Type :
Academic Journal
Accession number :
39581063
Full Text :
https://doi.org/10.1016/j.atherosclerosis.2024.119053