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Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents
First introduced during the late 1800s, radiation therapy is fundamental to the treatment of cancer. In developed countries, approximately 60% of all patients receive radiation therapy (also known as the sixty percenters), which makes radioresistance in cancer an important and, to date, unsolved, cl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039418/ https://www.ncbi.nlm.nih.gov/pubmed/27384589 http://dx.doi.org/10.3390/biom6030032 |
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author | Oronsky, Bryan Scicinski, Jan Kim, Michelle M. Cabrales, Pedro Salacz, Michael E. Carter, Corey A. Oronsky, Neil Lybeck, Harry Lybeck, Michelle Larson, Christopher Reid, Tony R. Oronsky, Arnold |
author_facet | Oronsky, Bryan Scicinski, Jan Kim, Michelle M. Cabrales, Pedro Salacz, Michael E. Carter, Corey A. Oronsky, Neil Lybeck, Harry Lybeck, Michelle Larson, Christopher Reid, Tony R. Oronsky, Arnold |
author_sort | Oronsky, Bryan |
collection | PubMed |
description | First introduced during the late 1800s, radiation therapy is fundamental to the treatment of cancer. In developed countries, approximately 60% of all patients receive radiation therapy (also known as the sixty percenters), which makes radioresistance in cancer an important and, to date, unsolved, clinical problem. Unfortunately, the therapeutic refractoriness of solid tumors is the rule not the exception, and the ubiquity of resistance also extends to standard chemotherapy, molecularly targeted therapy and immunotherapy. Based on extrapolation from recent clinical inroads with epigenetic agents to prime refractory tumors for maximum sensitivity to concurrent or subsequent therapies, the radioresistant phenotype is potentially reversible, since aberrant epigenetic mechanisms are critical contributors to the evolution of resistant subpopulations of malignant cells. Within the framework of a syllogism, this review explores the emerging link between epigenetics and the development of radioresistance and makes the case that a strategy of pre- or co-treatment with epigenetic agents has the potential to, not only derepress inappropriately silenced genes, but also increase reactive oxygen species production, resulting in the restoration of radiosensitivity. |
format | Online Article Text |
id | pubmed-5039418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50394182016-10-04 Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents Oronsky, Bryan Scicinski, Jan Kim, Michelle M. Cabrales, Pedro Salacz, Michael E. Carter, Corey A. Oronsky, Neil Lybeck, Harry Lybeck, Michelle Larson, Christopher Reid, Tony R. Oronsky, Arnold Biomolecules Review First introduced during the late 1800s, radiation therapy is fundamental to the treatment of cancer. In developed countries, approximately 60% of all patients receive radiation therapy (also known as the sixty percenters), which makes radioresistance in cancer an important and, to date, unsolved, clinical problem. Unfortunately, the therapeutic refractoriness of solid tumors is the rule not the exception, and the ubiquity of resistance also extends to standard chemotherapy, molecularly targeted therapy and immunotherapy. Based on extrapolation from recent clinical inroads with epigenetic agents to prime refractory tumors for maximum sensitivity to concurrent or subsequent therapies, the radioresistant phenotype is potentially reversible, since aberrant epigenetic mechanisms are critical contributors to the evolution of resistant subpopulations of malignant cells. Within the framework of a syllogism, this review explores the emerging link between epigenetics and the development of radioresistance and makes the case that a strategy of pre- or co-treatment with epigenetic agents has the potential to, not only derepress inappropriately silenced genes, but also increase reactive oxygen species production, resulting in the restoration of radiosensitivity. MDPI 2016-07-04 /pmc/articles/PMC5039418/ /pubmed/27384589 http://dx.doi.org/10.3390/biom6030032 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Oronsky, Bryan Scicinski, Jan Kim, Michelle M. Cabrales, Pedro Salacz, Michael E. Carter, Corey A. Oronsky, Neil Lybeck, Harry Lybeck, Michelle Larson, Christopher Reid, Tony R. Oronsky, Arnold Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title | Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title_full | Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title_fullStr | Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title_full_unstemmed | Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title_short | Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents |
title_sort | turning on the radio: epigenetic inhibitors as potential radiopriming agents |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5039418/ https://www.ncbi.nlm.nih.gov/pubmed/27384589 http://dx.doi.org/10.3390/biom6030032 |
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