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Epigenetic Modifications as Therapeutic Targets

Epigenetic modifications work with genetic mechanisms to determine transcriptional activity and, while somatically heritable they are also reversible, making them good therapeutic candidates. Epigenetic changes can precede disease pathology and thus are diagnostic indicators for risk, and can act as...

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Detalles Bibliográficos
Autores principales: Kelly, Theresa K, De Carvalho, Daniel D, Jones, Peter A
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022972/
https://www.ncbi.nlm.nih.gov/pubmed/20944599
http://dx.doi.org/10.1038/nbt.1678
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author Kelly, Theresa K
De Carvalho, Daniel D
Jones, Peter A
author_facet Kelly, Theresa K
De Carvalho, Daniel D
Jones, Peter A
author_sort Kelly, Theresa K
collection PubMed
description Epigenetic modifications work with genetic mechanisms to determine transcriptional activity and, while somatically heritable they are also reversible, making them good therapeutic candidates. Epigenetic changes can precede disease pathology and thus are diagnostic indicators for risk, and can act as prognostic indicators for disease progression. Histone deacetylase inhibitors and DNA methylation inhibitors have been FDA approved for several years and are clinically successful. More recently, histone methylation and microRNAs have also gained attention as potential therapeutic targets. The presence of multiple epigenetic aberrations within a diseased tissue and the abilities of cells to develop resistance suggest that combination therapies may be most beneficial. This review will focus on recent examples of using epigenetic modifications to evaluate disease risk, progression and clinical response and will describe the latest clinical advances in epigenetic therapies concentrating on treatments which combine epigenetic therapeutics with each other and with cytotoxic agents to increase clinical response.
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spelling pubmed-30229722012-04-01 Epigenetic Modifications as Therapeutic Targets Kelly, Theresa K De Carvalho, Daniel D Jones, Peter A Nat Biotechnol Article Epigenetic modifications work with genetic mechanisms to determine transcriptional activity and, while somatically heritable they are also reversible, making them good therapeutic candidates. Epigenetic changes can precede disease pathology and thus are diagnostic indicators for risk, and can act as prognostic indicators for disease progression. Histone deacetylase inhibitors and DNA methylation inhibitors have been FDA approved for several years and are clinically successful. More recently, histone methylation and microRNAs have also gained attention as potential therapeutic targets. The presence of multiple epigenetic aberrations within a diseased tissue and the abilities of cells to develop resistance suggest that combination therapies may be most beneficial. This review will focus on recent examples of using epigenetic modifications to evaluate disease risk, progression and clinical response and will describe the latest clinical advances in epigenetic therapies concentrating on treatments which combine epigenetic therapeutics with each other and with cytotoxic agents to increase clinical response. 2010-10 /pmc/articles/PMC3022972/ /pubmed/20944599 http://dx.doi.org/10.1038/nbt.1678 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kelly, Theresa K
De Carvalho, Daniel D
Jones, Peter A
Epigenetic Modifications as Therapeutic Targets
title Epigenetic Modifications as Therapeutic Targets
title_full Epigenetic Modifications as Therapeutic Targets
title_fullStr Epigenetic Modifications as Therapeutic Targets
title_full_unstemmed Epigenetic Modifications as Therapeutic Targets
title_short Epigenetic Modifications as Therapeutic Targets
title_sort epigenetic modifications as therapeutic targets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022972/
https://www.ncbi.nlm.nih.gov/pubmed/20944599
http://dx.doi.org/10.1038/nbt.1678
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