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It’s all in the combination: decoding the epigenome for cancer research and diagnostics

Genome regulation is governed by the dynamics of chromatin modifications. The extensive and diverse array of DNA and histone modifications allow multiple elements to act combinatorically and direct tissue-specific and cell-specific outcomes. Yet, our ability to elucidate these complex combinations a...

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Detalles Bibliográficos
Autores principales: Furth, Noa, Shema, Efrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168437/
https://www.ncbi.nlm.nih.gov/pubmed/35091256
http://dx.doi.org/10.1016/j.gde.2022.101899
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author Furth, Noa
Shema, Efrat
author_facet Furth, Noa
Shema, Efrat
author_sort Furth, Noa
collection PubMed
description Genome regulation is governed by the dynamics of chromatin modifications. The extensive and diverse array of DNA and histone modifications allow multiple elements to act combinatorically and direct tissue-specific and cell-specific outcomes. Yet, our ability to elucidate these complex combinations and link them to normal genome regulation, as well as understand their deregulation in cancer, has been hindered by the lack of suitable technologies. Here, we describe recent findings indicating the importance of the combinatorial epigenome, and novel methodologies to measure and characterize these combinations. These complementary methods span multiple disciplines, providing a means to decode epigenetic combinations and link them to biological outcomes. Finally, we discuss the promise of harnessing the rich combinatorial epigenetic information to improve cancer diagnostics and monitoring.
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spelling pubmed-91684372022-06-14 It’s all in the combination: decoding the epigenome for cancer research and diagnostics Furth, Noa Shema, Efrat Curr Opin Genet Dev Article Genome regulation is governed by the dynamics of chromatin modifications. The extensive and diverse array of DNA and histone modifications allow multiple elements to act combinatorically and direct tissue-specific and cell-specific outcomes. Yet, our ability to elucidate these complex combinations and link them to normal genome regulation, as well as understand their deregulation in cancer, has been hindered by the lack of suitable technologies. Here, we describe recent findings indicating the importance of the combinatorial epigenome, and novel methodologies to measure and characterize these combinations. These complementary methods span multiple disciplines, providing a means to decode epigenetic combinations and link them to biological outcomes. Finally, we discuss the promise of harnessing the rich combinatorial epigenetic information to improve cancer diagnostics and monitoring. Elsevier 2022-04 /pmc/articles/PMC9168437/ /pubmed/35091256 http://dx.doi.org/10.1016/j.gde.2022.101899 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Furth, Noa
Shema, Efrat
It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title_full It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title_fullStr It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title_full_unstemmed It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title_short It’s all in the combination: decoding the epigenome for cancer research and diagnostics
title_sort it’s all in the combination: decoding the epigenome for cancer research and diagnostics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168437/
https://www.ncbi.nlm.nih.gov/pubmed/35091256
http://dx.doi.org/10.1016/j.gde.2022.101899
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