Relevance of the epigenetic regulation exercised by hepatic microRNAs in the fatty liver arena: from the bedside to the bench

Non-alcoholic fatty liver disease (NAFLD) has become the leading cause of chronic liver disease worldwide, involving a spectrum of disturbances mainly characterized by fatty acid infiltration and fat deposition in the liver parenchyma. Given that alterations in epigenetic mechanisms have been associ...

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Detalles Bibliográficos
Autor: Latorre Luque, Jèssica
Tipo de recurso: tesis doctoral
Estado:Versión publicada
Fecha de publicación:2020
País:España
Institución:CBUC, CESCA
Repositorio:TDR. Tesis Doctorales en Red
OAI Identifier:oai:www.tdx.cat:10803/671499
Acceso en línea:http://hdl.handle.net/10803/671499
Access Level:acceso abierto
Palabra clave:MicroRNAs
Non-alcoholic fatty liver disease (NAFLD)
Fatty liver
Fetge gras
Hígado graso
Epigenetics
Epigenètica
Epigenética
Metabolism
Metabolisme
Triglycerides
Triglicèrids
Triglicéridos
Chronic liver diseases
Malalties hepàtiques cròniques
Enfermedades epáticas crónicas
575
616.3
Descripción
Sumario:Non-alcoholic fatty liver disease (NAFLD) has become the leading cause of chronic liver disease worldwide, involving a spectrum of disturbances mainly characterized by fatty acid infiltration and fat deposition in the liver parenchyma. Given that alterations in epigenetic mechanisms have been associated with hepatic metabolic disorders, we focused on the relevance of microRNAs (miRNAs) in the pathophysiology of NAFLD. In this thesis, an analysis of hepatic miRNAs comparing patients with and without NAFLD has shown that the disease is associated with an altered miRNA profile, and that the expression of specific miRNAs is related to changes in gene expression and impaired glucose and lipid metabolism. Additionally, altered regulation of miRNAs has been demonstrated through modulation of AMPK in cell and animal models. Finally, specific miRNAs were observed to partially rescued fatty acid overload and modified lipid profiles within hepatocytes, stressing their potential as epigenetic regulators to combat NAFLD