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miR-378a: a new emerging microRNA in metabolism.
Machado, Ivo F; Teodoro, João S; Palmeira, Carlos M; Rolo, Anabela P.
Afiliação
  • Machado IF; Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal.
  • Teodoro JS; CNC, Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
  • Palmeira CM; Department of Life Sciences, Faculty of Sciences and Technology, University of Coimbra, Calçada Martim de Freitas, 3000-456, Coimbra, Portugal.
  • Rolo AP; CNC, Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
Cell Mol Life Sci ; 77(10): 1947-1958, 2020 May.
Article em En | MEDLINE | ID: mdl-31748917
ABSTRACT
Metabolic diseases, such as type 2 diabetes or obesity, are the consequence of the disruption of the organism's metabolic pathways. The discovery of small non-coding RNAs-microRNAs (miRNAs)-as post-transcriptional gene regulators opened new doors for the development of novel strategies to combat said diseases. The two strands of miR-378a, miR-378a-3p, and miR-378a-5p are encoded in the Ppargc1b gene and have an active role in the regulation of several metabolic pathways such as mitochondrial metabolism and autophagy. Recent studies recognized miR-378a as an important regulator of energy and glucose homeostasis, highlighting it as a potential target for the improvement of metabolic dysregulation. In the present review, the current knowledge on miR-378a will be discussed with a particular emphasis on its biological functions and mechanisms of action in metabolism, mitochondria, and autophagy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: MicroRNAs / Redes e Vias Metabólicas / Doenças Metabólicas / Mitocôndrias Limite: Humans Idioma: En Revista: Cell Mol Life Sci Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: MicroRNAs / Redes e Vias Metabólicas / Doenças Metabólicas / Mitocôndrias Limite: Humans Idioma: En Revista: Cell Mol Life Sci Ano de publicação: 2020 Tipo de documento: Article