Show simple item record

dc.contributor.authorIturbe Rey, Santiago
dc.contributor.authorMaccali, Claudia
dc.contributor.authorArrese, Marco
dc.contributor.authorAspichueta Celaá, Patricia
dc.contributor.authorOliveira, Claudia P.
dc.contributor.authorCastro, Rui E.
dc.contributor.authorLapitz Dambolenea, Ainhoa
dc.contributor.authorIzquierdo Sánchez, Laura
dc.contributor.authorBujanda Fernández de Pierola, Luis ORCID
dc.contributor.authorPerugorria Montiel, María Jesús ORCID
dc.contributor.authorBañales Asurmendi, Jesús María
dc.contributor.authorRodrigues, Pedro M.
dc.date.accessioned2025-02-11T14:00:32Z
dc.date.available2025-02-11T14:00:32Z
dc.date.issued2025-01
dc.identifier.citationAtherosclerosis 400 : (2025) // Article ID 119053es_ES
dc.identifier.issn1879-1484
dc.identifier.issn0021-9150
dc.identifier.urihttp://hdl.handle.net/10810/72612
dc.description.abstractMetabolic 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.es_ES
dc.description.sponsorshipSpanish Carlos III Health Institute (ISCIII) [JMB (FIS PI18/01075, PI21/00922 and Miguel Servet CPII19/00008); MJP (FIS PI20/00186, PI23/01565); PMR (FIS PI23/01850 and Miguel Servet CP22/00073); JMB and PA (PMP21/00080)] cofinanced by “Fondo Europeo de Desarrollo Regional” (FEDER); CIBERehd (ISCIII): JMB, PMR, MJP, PA and LB, Spain; “Diputación Foral Gipuzkoa” (2023-CIEN-000008-01 to PMR and 2023-CIEN-000045-04-01 to MJP), Spain; Department of Health of the Basque Country (2023111017 to MJP and PA, 2020111077 and 2021111021 to JMB and PA; 2022111070 to PMR); La Caixa Scientific Foundation (JMB and REC: HR17-00601), Spain; “Fundación Científica de la Asociación Española Contra el Cáncer” (AECC Scientific Foundation: “Lab AECC 2023” AECC23/502 to PMR; AECC Postdoctoral grant POSTD246369IZQU to LI-S), Spain; Asociación Española para el Estudio del Hígado (AEEH, Juan Rodes Postdoctoral grant to LI-S); AMMF-The Cholangiocarcinoma Charity (EU/2019/AMMFt/001, to JMB and PMR), United Kingdom; PSC Partners US (to JMB and AL) and PSC Supports UK (to JMB and PMR). SI-R and LI-S received funds from the Department of Education of the Basque Country (PRE_2023_1_0021 and POS_2022_1_0041, respectively). MCIN/AEI/10.13039/501100011033 (PID2021- 124425OB-I00 to PA) co-financed by the European Regional Development Fund (ERDF); and Grupos consolidados Gobierno Vasco IT1476-22 to PA; MA was founded by Pontificia Universidad Católica de Chile (PBV2302); and Chilean Government through Fondo Nacional de Desarrollo Científico y Tecnológico (Fondecyt Project, 1241450 to MA); CM was financed by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Brasil (CAPES) – Finance Code 001.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2021-124425OB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectMASLDes_ES
dc.subjectMASHes_ES
dc.subjectlipotoxicityes_ES
dc.subjectlipidses_ES
dc.subjectfatty acidses_ES
dc.subjectcell deathes_ES
dc.subjectliver canceres_ES
dc.titleLipotoxicity-driven metabolic dysfunction-associated steatotic liver disease (MASLD)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND licensees_ES
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0021915024012255es_ES
dc.identifier.doi10.1016/j.atherosclerosis.2024.119053
dc.departamentoesBioquímica y biología moleculares_ES
dc.departamentoesFisiologíaes_ES
dc.departamentoesMedicinaes_ES
dc.departamentoeuBiokimika eta biologia molekularraes_ES
dc.departamentoeuFisiologiaes_ES
dc.departamentoeuMedikuntzaes_ES


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
Except where otherwise noted, this item's license is described as © 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license