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The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders

Peroxisome proliferator-activated receptors (PPARs) are ligand-modulated nuclear receptors that play pivotal roles in nutrient sensing, metabolism, and lipid-related processes. Correct control of their target genes requires tight regulation of the expression of different PPAR isoforms in each tissue...

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Autores principales: Porcuna, Jesús, Mínguez-Martínez, Jorge, Ricote, Mercedes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508752/
https://www.ncbi.nlm.nih.gov/pubmed/34638914
http://dx.doi.org/10.3390/ijms221910573
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author Porcuna, Jesús
Mínguez-Martínez, Jorge
Ricote, Mercedes
author_facet Porcuna, Jesús
Mínguez-Martínez, Jorge
Ricote, Mercedes
author_sort Porcuna, Jesús
collection PubMed
description Peroxisome proliferator-activated receptors (PPARs) are ligand-modulated nuclear receptors that play pivotal roles in nutrient sensing, metabolism, and lipid-related processes. Correct control of their target genes requires tight regulation of the expression of different PPAR isoforms in each tissue, and the dysregulation of PPAR-dependent transcriptional programs is linked to disorders, such as metabolic and immune diseases or cancer. Several PPAR regulators and PPAR-regulated factors are epigenetic effectors, including non-coding RNAs, epigenetic enzymes, histone modifiers, and DNA methyltransferases. In this review, we examine advances in PPARα and PPARγ-related epigenetic regulation in metabolic disorders, including obesity and diabetes, immune disorders, such as sclerosis and lupus, and a variety of cancers, providing new insights into the possible therapeutic exploitation of PPAR epigenetic modulation.
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spelling pubmed-85087522021-10-13 The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders Porcuna, Jesús Mínguez-Martínez, Jorge Ricote, Mercedes Int J Mol Sci Review Peroxisome proliferator-activated receptors (PPARs) are ligand-modulated nuclear receptors that play pivotal roles in nutrient sensing, metabolism, and lipid-related processes. Correct control of their target genes requires tight regulation of the expression of different PPAR isoforms in each tissue, and the dysregulation of PPAR-dependent transcriptional programs is linked to disorders, such as metabolic and immune diseases or cancer. Several PPAR regulators and PPAR-regulated factors are epigenetic effectors, including non-coding RNAs, epigenetic enzymes, histone modifiers, and DNA methyltransferases. In this review, we examine advances in PPARα and PPARγ-related epigenetic regulation in metabolic disorders, including obesity and diabetes, immune disorders, such as sclerosis and lupus, and a variety of cancers, providing new insights into the possible therapeutic exploitation of PPAR epigenetic modulation. MDPI 2021-09-30 /pmc/articles/PMC8508752/ /pubmed/34638914 http://dx.doi.org/10.3390/ijms221910573 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Porcuna, Jesús
Mínguez-Martínez, Jorge
Ricote, Mercedes
The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title_full The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title_fullStr The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title_full_unstemmed The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title_short The PPARα and PPARγ Epigenetic Landscape in Cancer and Immune and Metabolic Disorders
title_sort pparα and pparγ epigenetic landscape in cancer and immune and metabolic disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508752/
https://www.ncbi.nlm.nih.gov/pubmed/34638914
http://dx.doi.org/10.3390/ijms221910573
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