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Epigenetic modifications in rheumatoid arthritis

Over the last decades, genetic factors for rheumatoid diseases like the HLA haplotypes have been studied extensively. However, during the past years of research, it has become more and more evident that the influence of epigenetic processes on the development of rheumatic diseases is probably as str...

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Autores principales: Strietholt, Simon, Maurer, Britta, Peters, Marvin A, Pap, Thomas, Gay, Steffen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592785/
https://www.ncbi.nlm.nih.gov/pubmed/18947370
http://dx.doi.org/10.1186/ar2500
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author Strietholt, Simon
Maurer, Britta
Peters, Marvin A
Pap, Thomas
Gay, Steffen
author_facet Strietholt, Simon
Maurer, Britta
Peters, Marvin A
Pap, Thomas
Gay, Steffen
author_sort Strietholt, Simon
collection PubMed
description Over the last decades, genetic factors for rheumatoid diseases like the HLA haplotypes have been studied extensively. However, during the past years of research, it has become more and more evident that the influence of epigenetic processes on the development of rheumatic diseases is probably as strong as the genetic background of a patient. Epigenetic processes are heritable changes in gene expression without alteration of the nucleotide sequence. Such modifications include chromatin methylation and post-translational modification of histones or other chromatin-associated proteins. The latter comprise the addition of methyl, acetyl, and phosphoryl groups or even larger moieties such as binding of ubiquitin or small ubiquitin-like modifier. The combinatory nature of these processes forms a complex network of epigenetic modifications that regulate gene expression through activation or silencing of genes. This review provides insight into the role of epigenetic alterations in the pathogenesis of rheumatoid arthritis and points out how a better understanding of such mechanisms may lead to novel therapeutic strategies.
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spelling pubmed-25927852008-12-03 Epigenetic modifications in rheumatoid arthritis Strietholt, Simon Maurer, Britta Peters, Marvin A Pap, Thomas Gay, Steffen Arthritis Res Ther Review Over the last decades, genetic factors for rheumatoid diseases like the HLA haplotypes have been studied extensively. However, during the past years of research, it has become more and more evident that the influence of epigenetic processes on the development of rheumatic diseases is probably as strong as the genetic background of a patient. Epigenetic processes are heritable changes in gene expression without alteration of the nucleotide sequence. Such modifications include chromatin methylation and post-translational modification of histones or other chromatin-associated proteins. The latter comprise the addition of methyl, acetyl, and phosphoryl groups or even larger moieties such as binding of ubiquitin or small ubiquitin-like modifier. The combinatory nature of these processes forms a complex network of epigenetic modifications that regulate gene expression through activation or silencing of genes. This review provides insight into the role of epigenetic alterations in the pathogenesis of rheumatoid arthritis and points out how a better understanding of such mechanisms may lead to novel therapeutic strategies. BioMed Central 2008 2008-10-10 /pmc/articles/PMC2592785/ /pubmed/18947370 http://dx.doi.org/10.1186/ar2500 Text en Copyright © 2008 BioMed Central Ltd
spellingShingle Review
Strietholt, Simon
Maurer, Britta
Peters, Marvin A
Pap, Thomas
Gay, Steffen
Epigenetic modifications in rheumatoid arthritis
title Epigenetic modifications in rheumatoid arthritis
title_full Epigenetic modifications in rheumatoid arthritis
title_fullStr Epigenetic modifications in rheumatoid arthritis
title_full_unstemmed Epigenetic modifications in rheumatoid arthritis
title_short Epigenetic modifications in rheumatoid arthritis
title_sort epigenetic modifications in rheumatoid arthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592785/
https://www.ncbi.nlm.nih.gov/pubmed/18947370
http://dx.doi.org/10.1186/ar2500
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