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Real-Time Monitoring of Cisplatin-Induced Cell Death

Since the discovery of cisplatin more than 40 years ago and its clinical introduction in the 1970s an enormous amount of research has gone into elucidating the mechanism of action of cisplatin on tumor cells. With a novel cell biosensor chip system allowing continuous monitoring of respiration, glyc...

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Autores principales: Alborzinia, Hamed, Can, Suzan, Holenya, Pavlo, Scholl, Catharina, Lederer, Elke, Kitanovic, Igor, Wölfl, Stefan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095603/
https://www.ncbi.nlm.nih.gov/pubmed/21603599
http://dx.doi.org/10.1371/journal.pone.0019714
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author Alborzinia, Hamed
Can, Suzan
Holenya, Pavlo
Scholl, Catharina
Lederer, Elke
Kitanovic, Igor
Wölfl, Stefan
author_facet Alborzinia, Hamed
Can, Suzan
Holenya, Pavlo
Scholl, Catharina
Lederer, Elke
Kitanovic, Igor
Wölfl, Stefan
author_sort Alborzinia, Hamed
collection PubMed
description Since the discovery of cisplatin more than 40 years ago and its clinical introduction in the 1970s an enormous amount of research has gone into elucidating the mechanism of action of cisplatin on tumor cells. With a novel cell biosensor chip system allowing continuous monitoring of respiration, glycolysis, and impedance we followed cisplatin treatment of different cancer cell lines in real-time. Our measurements reveal a first effect on respiration, in all cisplatin treated cell lines, followed with a significant delay by interference with glycolysis in HT-29, HCT-116, HepG2, and MCF-7 cells but not in the cisplatin-resistant cell line MDA-MB-231. Most strikingly, cell death started in all cisplatin-sensitive cell lines within 8 to 11 h of treatment, indicating a clear time frame from exposure, first response to cisplatin lesions, to cell fate decision. The time points of most significant changes were selected for more detailed analysis of cisplatin response in the breast cancer cell line MCF-7. Phosphorylation of selected signal transduction mediators connected with cellular proliferation, as well as changes in gene expression, were analyzed in samples obtained directly from sensor chips at the time points when changes in glycolysis and impedance occurred. Our online cell biosensor measurements reveal for the first time the time scale of metabolic response until onset of cell death under cisplatin treatment, which is in good agreement with models of p53-mediated cell fate decision.
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spelling pubmed-30956032011-05-19 Real-Time Monitoring of Cisplatin-Induced Cell Death Alborzinia, Hamed Can, Suzan Holenya, Pavlo Scholl, Catharina Lederer, Elke Kitanovic, Igor Wölfl, Stefan PLoS One Research Article Since the discovery of cisplatin more than 40 years ago and its clinical introduction in the 1970s an enormous amount of research has gone into elucidating the mechanism of action of cisplatin on tumor cells. With a novel cell biosensor chip system allowing continuous monitoring of respiration, glycolysis, and impedance we followed cisplatin treatment of different cancer cell lines in real-time. Our measurements reveal a first effect on respiration, in all cisplatin treated cell lines, followed with a significant delay by interference with glycolysis in HT-29, HCT-116, HepG2, and MCF-7 cells but not in the cisplatin-resistant cell line MDA-MB-231. Most strikingly, cell death started in all cisplatin-sensitive cell lines within 8 to 11 h of treatment, indicating a clear time frame from exposure, first response to cisplatin lesions, to cell fate decision. The time points of most significant changes were selected for more detailed analysis of cisplatin response in the breast cancer cell line MCF-7. Phosphorylation of selected signal transduction mediators connected with cellular proliferation, as well as changes in gene expression, were analyzed in samples obtained directly from sensor chips at the time points when changes in glycolysis and impedance occurred. Our online cell biosensor measurements reveal for the first time the time scale of metabolic response until onset of cell death under cisplatin treatment, which is in good agreement with models of p53-mediated cell fate decision. Public Library of Science 2011-05-16 /pmc/articles/PMC3095603/ /pubmed/21603599 http://dx.doi.org/10.1371/journal.pone.0019714 Text en Alborzinia 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Alborzinia, Hamed
Can, Suzan
Holenya, Pavlo
Scholl, Catharina
Lederer, Elke
Kitanovic, Igor
Wölfl, Stefan
Real-Time Monitoring of Cisplatin-Induced Cell Death
title Real-Time Monitoring of Cisplatin-Induced Cell Death
title_full Real-Time Monitoring of Cisplatin-Induced Cell Death
title_fullStr Real-Time Monitoring of Cisplatin-Induced Cell Death
title_full_unstemmed Real-Time Monitoring of Cisplatin-Induced Cell Death
title_short Real-Time Monitoring of Cisplatin-Induced Cell Death
title_sort real-time monitoring of cisplatin-induced cell death
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095603/
https://www.ncbi.nlm.nih.gov/pubmed/21603599
http://dx.doi.org/10.1371/journal.pone.0019714
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