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Epigenetics in Cancer: A Hematological Perspective

For several decades, we have known that epigenetic regulation is disrupted in cancer. Recently, an increasing body of data suggests epigenetics might be an intersection of current cancer research trends: next generation sequencing, immunology, metabolomics, and cell aging. The new emphasis on epigen...

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Detalles Bibliográficos
Autores principales: Stahl, Maximilian, Kohrman, Nathan, Gore, Steven D., Kim, Tae Kon, Zeidan, Amer M., Prebet, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065123/
https://www.ncbi.nlm.nih.gov/pubmed/27723796
http://dx.doi.org/10.1371/journal.pgen.1006193
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author Stahl, Maximilian
Kohrman, Nathan
Gore, Steven D.
Kim, Tae Kon
Zeidan, Amer M.
Prebet, Thomas
author_facet Stahl, Maximilian
Kohrman, Nathan
Gore, Steven D.
Kim, Tae Kon
Zeidan, Amer M.
Prebet, Thomas
author_sort Stahl, Maximilian
collection PubMed
description For several decades, we have known that epigenetic regulation is disrupted in cancer. Recently, an increasing body of data suggests epigenetics might be an intersection of current cancer research trends: next generation sequencing, immunology, metabolomics, and cell aging. The new emphasis on epigenetics is also related to the increasing production of drugs capable of interfering with epigenetic mechanisms and able to trigger clinical responses in even advanced phase patients. In this review, we will use myeloid malignancies as proof of concept examples of how epigenetic mechanisms can trigger or promote oncogenesis. We will also show how epigenetic mechanisms are related to genetic aberrations, and how they affect other systems, like immune response. Finally, we will show how we can try to influence the fate of cancer cells with epigenetic therapy.
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spelling pubmed-50651232016-10-27 Epigenetics in Cancer: A Hematological Perspective Stahl, Maximilian Kohrman, Nathan Gore, Steven D. Kim, Tae Kon Zeidan, Amer M. Prebet, Thomas PLoS Genet Review For several decades, we have known that epigenetic regulation is disrupted in cancer. Recently, an increasing body of data suggests epigenetics might be an intersection of current cancer research trends: next generation sequencing, immunology, metabolomics, and cell aging. The new emphasis on epigenetics is also related to the increasing production of drugs capable of interfering with epigenetic mechanisms and able to trigger clinical responses in even advanced phase patients. In this review, we will use myeloid malignancies as proof of concept examples of how epigenetic mechanisms can trigger or promote oncogenesis. We will also show how epigenetic mechanisms are related to genetic aberrations, and how they affect other systems, like immune response. Finally, we will show how we can try to influence the fate of cancer cells with epigenetic therapy. Public Library of Science 2016-10-10 /pmc/articles/PMC5065123/ /pubmed/27723796 http://dx.doi.org/10.1371/journal.pgen.1006193 Text en © 2016 Stahl et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Stahl, Maximilian
Kohrman, Nathan
Gore, Steven D.
Kim, Tae Kon
Zeidan, Amer M.
Prebet, Thomas
Epigenetics in Cancer: A Hematological Perspective
title Epigenetics in Cancer: A Hematological Perspective
title_full Epigenetics in Cancer: A Hematological Perspective
title_fullStr Epigenetics in Cancer: A Hematological Perspective
title_full_unstemmed Epigenetics in Cancer: A Hematological Perspective
title_short Epigenetics in Cancer: A Hematological Perspective
title_sort epigenetics in cancer: a hematological perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065123/
https://www.ncbi.nlm.nih.gov/pubmed/27723796
http://dx.doi.org/10.1371/journal.pgen.1006193
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