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Addressing intra-tumoral heterogeneity and therapy resistance

In the last several years, our appreciation of intra-tumoral heterogeneity has greatly increased due to accumulating evidence for the co-existence of genetically and epigenetically divergent cancer cells residing in different microenvironments within a tumor. Herein, we review recent literature disc...

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Detalles Bibliográficos
Autores principales: Rybinski, Brad, Yun, Kyuson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342165/
https://www.ncbi.nlm.nih.gov/pubmed/27608848
http://dx.doi.org/10.18632/oncotarget.11875
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author Rybinski, Brad
Yun, Kyuson
author_facet Rybinski, Brad
Yun, Kyuson
author_sort Rybinski, Brad
collection PubMed
description In the last several years, our appreciation of intra-tumoral heterogeneity has greatly increased due to accumulating evidence for the co-existence of genetically and epigenetically divergent cancer cells residing in different microenvironments within a tumor. Herein, we review recent literature discussing intra-tumoral heterogeneity in the context of therapy resistance mechanisms at the genetic, epigenetic and microenvironmental levels. We illustrate the influence of tumor microenvironment on therapy resistance and epigenetic states of cancer cells by highlighting the role of cancer stem cells in therapy resistance. We also summarize different strategies that have been employed to address various resistance mechanisms at genetic, epigenetic, and microenvironmental levels in preclinical and clinical studies. We propose that future personalized cancer therapy design needs to incorporate dynamic and comprehensive analyses of tumor heterogeneity landscape and multi-dimensional mechanisms of therapy resistance.
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spelling pubmed-53421652017-03-24 Addressing intra-tumoral heterogeneity and therapy resistance Rybinski, Brad Yun, Kyuson Oncotarget Review In the last several years, our appreciation of intra-tumoral heterogeneity has greatly increased due to accumulating evidence for the co-existence of genetically and epigenetically divergent cancer cells residing in different microenvironments within a tumor. Herein, we review recent literature discussing intra-tumoral heterogeneity in the context of therapy resistance mechanisms at the genetic, epigenetic and microenvironmental levels. We illustrate the influence of tumor microenvironment on therapy resistance and epigenetic states of cancer cells by highlighting the role of cancer stem cells in therapy resistance. We also summarize different strategies that have been employed to address various resistance mechanisms at genetic, epigenetic, and microenvironmental levels in preclinical and clinical studies. We propose that future personalized cancer therapy design needs to incorporate dynamic and comprehensive analyses of tumor heterogeneity landscape and multi-dimensional mechanisms of therapy resistance. Impact Journals LLC 2016-09-06 /pmc/articles/PMC5342165/ /pubmed/27608848 http://dx.doi.org/10.18632/oncotarget.11875 Text en Copyright: © 2016 Rybinski and Yun http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Rybinski, Brad
Yun, Kyuson
Addressing intra-tumoral heterogeneity and therapy resistance
title Addressing intra-tumoral heterogeneity and therapy resistance
title_full Addressing intra-tumoral heterogeneity and therapy resistance
title_fullStr Addressing intra-tumoral heterogeneity and therapy resistance
title_full_unstemmed Addressing intra-tumoral heterogeneity and therapy resistance
title_short Addressing intra-tumoral heterogeneity and therapy resistance
title_sort addressing intra-tumoral heterogeneity and therapy resistance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342165/
https://www.ncbi.nlm.nih.gov/pubmed/27608848
http://dx.doi.org/10.18632/oncotarget.11875
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