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PPAR Medicines and Human Disease: The ABCs of It All

ATP-dependent binding cassette (ABC) transporters are a family of transmembrane proteins that pump a variety of hydrophobic compounds across cellular and subcellular barriers and are implicated in human diseases such as cancer and atherosclerosis. Inhibition of ABC transporter activity showed promis...

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Detalles Bibliográficos
Autores principales: Apostoli, Anthony J., Nicol, Christopher J. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423947/
https://www.ncbi.nlm.nih.gov/pubmed/22919365
http://dx.doi.org/10.1155/2012/504918
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author Apostoli, Anthony J.
Nicol, Christopher J. B.
author_facet Apostoli, Anthony J.
Nicol, Christopher J. B.
author_sort Apostoli, Anthony J.
collection PubMed
description ATP-dependent binding cassette (ABC) transporters are a family of transmembrane proteins that pump a variety of hydrophobic compounds across cellular and subcellular barriers and are implicated in human diseases such as cancer and atherosclerosis. Inhibition of ABC transporter activity showed promise in early preclinical studies; however, the outcomes in clinical trials with these agents have not been as encouraging. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that regulate genes involved in fat and glucose metabolism, and inflammation. Activation of PPAR signaling is also reported to regulate ABC gene expression. This suggests the potential of PPAR medicines as a novel means of controlling ABC transporter activity at the transcriptional level. This paper summarizes the advances made in understanding how PPAR medicines affect ABC transporters, and the potential implications for impacting on human diseases, in particular with respect to cancer and atherosclerosis.
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spelling pubmed-34239472012-08-23 PPAR Medicines and Human Disease: The ABCs of It All Apostoli, Anthony J. Nicol, Christopher J. B. PPAR Res Review Article ATP-dependent binding cassette (ABC) transporters are a family of transmembrane proteins that pump a variety of hydrophobic compounds across cellular and subcellular barriers and are implicated in human diseases such as cancer and atherosclerosis. Inhibition of ABC transporter activity showed promise in early preclinical studies; however, the outcomes in clinical trials with these agents have not been as encouraging. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that regulate genes involved in fat and glucose metabolism, and inflammation. Activation of PPAR signaling is also reported to regulate ABC gene expression. This suggests the potential of PPAR medicines as a novel means of controlling ABC transporter activity at the transcriptional level. This paper summarizes the advances made in understanding how PPAR medicines affect ABC transporters, and the potential implications for impacting on human diseases, in particular with respect to cancer and atherosclerosis. Hindawi Publishing Corporation 2012 2012-08-07 /pmc/articles/PMC3423947/ /pubmed/22919365 http://dx.doi.org/10.1155/2012/504918 Text en Copyright © 2012 A. J. Apostoli and C. J. B. Nicol. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Apostoli, Anthony J.
Nicol, Christopher J. B.
PPAR Medicines and Human Disease: The ABCs of It All
title PPAR Medicines and Human Disease: The ABCs of It All
title_full PPAR Medicines and Human Disease: The ABCs of It All
title_fullStr PPAR Medicines and Human Disease: The ABCs of It All
title_full_unstemmed PPAR Medicines and Human Disease: The ABCs of It All
title_short PPAR Medicines and Human Disease: The ABCs of It All
title_sort ppar medicines and human disease: the abcs of it all
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3423947/
https://www.ncbi.nlm.nih.gov/pubmed/22919365
http://dx.doi.org/10.1155/2012/504918
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