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The role of epigenetics in the biology of multiple myeloma

Several recent studies have highlighted the biological complexity of multiple myeloma (MM) that arises as a result of several disrupted cancer pathways. Apart from the central role of genetic abnormalities, epigenetic aberrations have also been shown to be important players in the development of MM,...

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Detalles Bibliográficos
Autores principales: Dimopoulos, K, Gimsing, P, Grønbæk, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042299/
https://www.ncbi.nlm.nih.gov/pubmed/24786391
http://dx.doi.org/10.1038/bcj.2014.29
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author Dimopoulos, K
Gimsing, P
Grønbæk, K
author_facet Dimopoulos, K
Gimsing, P
Grønbæk, K
author_sort Dimopoulos, K
collection PubMed
description Several recent studies have highlighted the biological complexity of multiple myeloma (MM) that arises as a result of several disrupted cancer pathways. Apart from the central role of genetic abnormalities, epigenetic aberrations have also been shown to be important players in the development of MM, and a lot of research during the past decades has focused on the ways DNA methylation, histone modifications and noncoding RNAs contribute to the pathobiology of MM. This has led to, apart from better understanding of the disease biology, the development of epigenetic drugs, such as histone deacetylase inhibitors that are already used in clinical trials in MM with promising results. This review will present the role of epigenetic abnormalities in MM and how these can affect specific pathways, and focus on the potential of novel ‘epidrugs' as future treatment modalities for MM.
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spelling pubmed-40422992014-06-12 The role of epigenetics in the biology of multiple myeloma Dimopoulos, K Gimsing, P Grønbæk, K Blood Cancer J Review Several recent studies have highlighted the biological complexity of multiple myeloma (MM) that arises as a result of several disrupted cancer pathways. Apart from the central role of genetic abnormalities, epigenetic aberrations have also been shown to be important players in the development of MM, and a lot of research during the past decades has focused on the ways DNA methylation, histone modifications and noncoding RNAs contribute to the pathobiology of MM. This has led to, apart from better understanding of the disease biology, the development of epigenetic drugs, such as histone deacetylase inhibitors that are already used in clinical trials in MM with promising results. This review will present the role of epigenetic abnormalities in MM and how these can affect specific pathways, and focus on the potential of novel ‘epidrugs' as future treatment modalities for MM. Nature Publishing Group 2014-05 2014-05-02 /pmc/articles/PMC4042299/ /pubmed/24786391 http://dx.doi.org/10.1038/bcj.2014.29 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Review
Dimopoulos, K
Gimsing, P
Grønbæk, K
The role of epigenetics in the biology of multiple myeloma
title The role of epigenetics in the biology of multiple myeloma
title_full The role of epigenetics in the biology of multiple myeloma
title_fullStr The role of epigenetics in the biology of multiple myeloma
title_full_unstemmed The role of epigenetics in the biology of multiple myeloma
title_short The role of epigenetics in the biology of multiple myeloma
title_sort role of epigenetics in the biology of multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042299/
https://www.ncbi.nlm.nih.gov/pubmed/24786391
http://dx.doi.org/10.1038/bcj.2014.29
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