Skip navigation
Use este identificador para citar ou linkar para este item: http://repositorio2.unb.br/jspui/handle/10482/40951
Arquivos associados a este item:
Arquivo Descrição TamanhoFormato 
ARTIGO_ImpactAdiposeTissue.pdf2,48 MBAdobe PDFVisualizar/Abrir
Registro completo de metadados
Campo DCValorIdioma
dc.contributor.authorHeyn, Gabriella Simões-
dc.contributor.authorCorrêa, Luís Henrique-
dc.contributor.authorMagalhães, Kelly Grace-
dc.date.accessioned2021-05-19T19:32:23Z-
dc.date.available2021-05-19T19:32:23Z-
dc.date.issued2020-
dc.identifier.citationHEYN, Gabriella Simões; CORRÊA, Luís Henrique; MAGALHÃES, Kelly Grace. The impact of adipose tissue–derived miRNAs in metabolic syndrome, obesity, and cancer. Frontier in Endocrinology, v. 11, 563816, 2020. DOI: 10.3389/fendo.2020.563816. Disponível em: https://www.frontiersin.org/articles/10.3389/fendo.2020.563816/full. Acesso em: 14 maio 2021.pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/40951-
dc.language.isoInglêspt_BR
dc.publisherFrontierspt_BR
dc.rightsAcesso Abertopt_BR
dc.titleThe impact of adipose tissue–derived miRNAs in metabolic syndrome, obesity, and cancerpt_BR
dc.typeArtigopt_BR
dc.subject.keywordMicroRNApt_BR
dc.subject.keywordTecido adiposopt_BR
dc.subject.keywordObesidadept_BR
dc.subject.keywordCâncerpt_BR
dc.subject.keywordSíndrome metabólicapt_BR
dc.rights.license(CC BY) - Copyright © 2020 Heyn, Correa and Magalhães. This is an open-access article ̂ distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.pt_BR
dc.identifier.doihttps://doi.org/10.3389/fendo.2020.563816pt_BR
dc.description.abstract1Obesity is a multifactorial and complex condition that is characterized by abnormal and excessive white adipose tissue accumulation, which can lead to the development of metabolic diseases, such as type 2 diabetes mellitus, nonalcoholic fatty liver disease, cardiovascular diseases, and several types of cancer. Obesity is characterized by excessive adipose tissue accumulation and associated with alterations in immunity, displaying a chronic low-grade inflammation profile. Adipose tissue is a dynamic and complex endocrine organ composed not only by adipocytes, but several immunological cells, which can secrete hormones, cytokines and many other factors capable of regulating metabolic homeostasis and several critical biological pathways. Remarkably, adipose tissue is a major source of circulating microRNAs (miRNAs), recently described as a novel form of adipokines. Several adipose tissue–derived miRNAs are deeply associated with adipocytes differentiation and have been identified with an essential role in obesity-associated inflammation, insulin resistance, and tumor microenvironment. During obesity, adipose tissue can completely change the profile of the secreted miRNAs, influencing circulating miRNAs and impacting the development of different pathological conditions, such as obesity, metabolic syndrome, and cancer. In this review, we discuss how miRNAs can act as epigenetic regulators affecting adipogenesis, adipocyte differentiation, lipid metabolism, browning of the white adipose tissue, glucose homeostasis, and insulin resistance, impacting deeply obesity and metabolic diseases. Moreover, we characterize how miRNAs can often act as oncogenic and tumor suppressor molecules, significantly modulating cancer establishment and progression. Furthermore, we highlight in this manuscript how adipose tissue–derived miRNAs can function as important new therapeutic targets.pt_BR
Aparece nas coleções:Artigos publicados em periódicos e afins

Mostrar registro simples do item Visualizar estatísticas



Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.