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Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity

Chromosome instability (CIN) is defined as an increased rate of chromosome gains and losses that manifests as cell-to-cell karyotypic heterogeneity and drives cancer initiation and evolution. Current research efforts are aimed at identifying the etiological origins of CIN, establishing its roles in...

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Autores principales: Lepage, Chloe C., Morden, Claire R., Palmer, Michaela C. L., Nachtigal, Mark W., McManus, Kirk J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406658/
https://www.ncbi.nlm.nih.gov/pubmed/30781398
http://dx.doi.org/10.3390/cancers11020226
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author Lepage, Chloe C.
Morden, Claire R.
Palmer, Michaela C. L.
Nachtigal, Mark W.
McManus, Kirk J.
author_facet Lepage, Chloe C.
Morden, Claire R.
Palmer, Michaela C. L.
Nachtigal, Mark W.
McManus, Kirk J.
author_sort Lepage, Chloe C.
collection PubMed
description Chromosome instability (CIN) is defined as an increased rate of chromosome gains and losses that manifests as cell-to-cell karyotypic heterogeneity and drives cancer initiation and evolution. Current research efforts are aimed at identifying the etiological origins of CIN, establishing its roles in cancer pathogenesis, understanding its implications for patient prognosis, and developing novel therapeutics that are capable of exploiting CIN. Thus, the ability to accurately identify and evaluate CIN is critical within both research and clinical settings. Here, we provide an overview of quantitative single cell approaches that evaluate and resolve cell-to-cell heterogeneity and CIN, and discuss considerations when selecting the most appropriate approach to suit both research and clinical contexts.
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spelling pubmed-64066582019-03-21 Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity Lepage, Chloe C. Morden, Claire R. Palmer, Michaela C. L. Nachtigal, Mark W. McManus, Kirk J. Cancers (Basel) Review Chromosome instability (CIN) is defined as an increased rate of chromosome gains and losses that manifests as cell-to-cell karyotypic heterogeneity and drives cancer initiation and evolution. Current research efforts are aimed at identifying the etiological origins of CIN, establishing its roles in cancer pathogenesis, understanding its implications for patient prognosis, and developing novel therapeutics that are capable of exploiting CIN. Thus, the ability to accurately identify and evaluate CIN is critical within both research and clinical settings. Here, we provide an overview of quantitative single cell approaches that evaluate and resolve cell-to-cell heterogeneity and CIN, and discuss considerations when selecting the most appropriate approach to suit both research and clinical contexts. MDPI 2019-02-15 /pmc/articles/PMC6406658/ /pubmed/30781398 http://dx.doi.org/10.3390/cancers11020226 Text en © 2019 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
Lepage, Chloe C.
Morden, Claire R.
Palmer, Michaela C. L.
Nachtigal, Mark W.
McManus, Kirk J.
Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title_full Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title_fullStr Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title_full_unstemmed Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title_short Detecting Chromosome Instability in Cancer: Approaches to Resolve Cell-to-Cell Heterogeneity
title_sort detecting chromosome instability in cancer: approaches to resolve cell-to-cell heterogeneity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406658/
https://www.ncbi.nlm.nih.gov/pubmed/30781398
http://dx.doi.org/10.3390/cancers11020226
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