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Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis

Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In...

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Detalles Bibliográficos
Autores principales: Chin, Sue, Hughes, Michael P, Coley, Helen M, Labeed, Fatima H
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426800/
https://www.ncbi.nlm.nih.gov/pubmed/17717973
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author Chin, Sue
Hughes, Michael P
Coley, Helen M
Labeed, Fatima H
author_facet Chin, Sue
Hughes, Michael P
Coley, Helen M
Labeed, Fatima H
author_sort Chin, Sue
collection PubMed
description Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In this paper, we describe the application of the electrical phenomenon dielectrophoresis for detecting apoptosis at very early stages after drug induction, on the basis of changes in electrophysiological properties. Our studies have revealed that K562 (human myelogenous leukemia) cells show a persistent elevation in the cytoplasmic conductivity occurring as early as 30 minutes following exposure to staurosporine. This method therefore allows a far more rapid detection method than existing biochemical marker methods.
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spelling pubmed-24268002008-06-20 Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis Chin, Sue Hughes, Michael P Coley, Helen M Labeed, Fatima H Int J Nanomedicine Original Research Apoptosis, or programmed cell death, is a vital cellular process responsible for causing cells to self-terminate at the end of their useful life. Abrogation of this process is commonly linked to cancer, and rapid detection of apoptosis in vitro is vital to the discovery of new anti-cancer drugs. In this paper, we describe the application of the electrical phenomenon dielectrophoresis for detecting apoptosis at very early stages after drug induction, on the basis of changes in electrophysiological properties. Our studies have revealed that K562 (human myelogenous leukemia) cells show a persistent elevation in the cytoplasmic conductivity occurring as early as 30 minutes following exposure to staurosporine. This method therefore allows a far more rapid detection method than existing biochemical marker methods. Dove Medical Press 2006-09 /pmc/articles/PMC2426800/ /pubmed/17717973 Text en © 2006 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Chin, Sue
Hughes, Michael P
Coley, Helen M
Labeed, Fatima H
Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title_full Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title_fullStr Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title_full_unstemmed Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title_short Rapid assessment of early biophysical changes in K562 cells during apoptosis determined using dielectrophoresis
title_sort rapid assessment of early biophysical changes in k562 cells during apoptosis determined using dielectrophoresis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426800/
https://www.ncbi.nlm.nih.gov/pubmed/17717973
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