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Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells

Tumor Treating Fields (TTFields) are low intensity, intermediate frequency, alternating electric fields. TTFields are a unique anti-mitotic treatment modality delivered in a continuous, noninvasive manner to the region of a tumor. It was previously postulated that by exerting directional forces on h...

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Autores principales: Giladi, Moshe, Schneiderman, Rosa S, Voloshin, Tali, Porat, Yaara, Munster, Mijal, Blat, Roni, Sherbo, Shay, Bomzon, Zeev, Urman, Noa, Itzhaki, Aviran, Cahal, Shay, Shteingauz, Anna, Chaudhry, Aafia, Kirson, Eilon D, Weinberg, Uri, Palti, Yoram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676010/
https://www.ncbi.nlm.nih.gov/pubmed/26658786
http://dx.doi.org/10.1038/srep18046
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author Giladi, Moshe
Schneiderman, Rosa S
Voloshin, Tali
Porat, Yaara
Munster, Mijal
Blat, Roni
Sherbo, Shay
Bomzon, Zeev
Urman, Noa
Itzhaki, Aviran
Cahal, Shay
Shteingauz, Anna
Chaudhry, Aafia
Kirson, Eilon D
Weinberg, Uri
Palti, Yoram
author_facet Giladi, Moshe
Schneiderman, Rosa S
Voloshin, Tali
Porat, Yaara
Munster, Mijal
Blat, Roni
Sherbo, Shay
Bomzon, Zeev
Urman, Noa
Itzhaki, Aviran
Cahal, Shay
Shteingauz, Anna
Chaudhry, Aafia
Kirson, Eilon D
Weinberg, Uri
Palti, Yoram
author_sort Giladi, Moshe
collection PubMed
description Tumor Treating Fields (TTFields) are low intensity, intermediate frequency, alternating electric fields. TTFields are a unique anti-mitotic treatment modality delivered in a continuous, noninvasive manner to the region of a tumor. It was previously postulated that by exerting directional forces on highly polar intracellular elements during mitosis, TTFields could disrupt the normal assembly of spindle microtubules. However there is limited evidence directly linking TTFields to an effect on microtubules. Here we report that TTFields decrease the ratio between polymerized and total tubulin, and prevent proper mitotic spindle assembly. The aberrant mitotic events induced by TTFields lead to abnormal chromosome segregation, cellular multinucleation, and caspase dependent apoptosis of daughter cells. The effect of TTFields on cell viability and clonogenic survival substantially depends upon the cell division rate. We show that by extending the duration of exposure to TTFields, slowly dividing cells can be affected to a similar extent as rapidly dividing cells.
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spelling pubmed-46760102015-12-16 Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells Giladi, Moshe Schneiderman, Rosa S Voloshin, Tali Porat, Yaara Munster, Mijal Blat, Roni Sherbo, Shay Bomzon, Zeev Urman, Noa Itzhaki, Aviran Cahal, Shay Shteingauz, Anna Chaudhry, Aafia Kirson, Eilon D Weinberg, Uri Palti, Yoram Sci Rep Article Tumor Treating Fields (TTFields) are low intensity, intermediate frequency, alternating electric fields. TTFields are a unique anti-mitotic treatment modality delivered in a continuous, noninvasive manner to the region of a tumor. It was previously postulated that by exerting directional forces on highly polar intracellular elements during mitosis, TTFields could disrupt the normal assembly of spindle microtubules. However there is limited evidence directly linking TTFields to an effect on microtubules. Here we report that TTFields decrease the ratio between polymerized and total tubulin, and prevent proper mitotic spindle assembly. The aberrant mitotic events induced by TTFields lead to abnormal chromosome segregation, cellular multinucleation, and caspase dependent apoptosis of daughter cells. The effect of TTFields on cell viability and clonogenic survival substantially depends upon the cell division rate. We show that by extending the duration of exposure to TTFields, slowly dividing cells can be affected to a similar extent as rapidly dividing cells. Nature Publishing Group 2015-12-11 /pmc/articles/PMC4676010/ /pubmed/26658786 http://dx.doi.org/10.1038/srep18046 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Giladi, Moshe
Schneiderman, Rosa S
Voloshin, Tali
Porat, Yaara
Munster, Mijal
Blat, Roni
Sherbo, Shay
Bomzon, Zeev
Urman, Noa
Itzhaki, Aviran
Cahal, Shay
Shteingauz, Anna
Chaudhry, Aafia
Kirson, Eilon D
Weinberg, Uri
Palti, Yoram
Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title_full Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title_fullStr Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title_full_unstemmed Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title_short Mitotic Spindle Disruption by Alternating Electric Fields Leads to Improper Chromosome Segregation and Mitotic Catastrophe in Cancer Cells
title_sort mitotic spindle disruption by alternating electric fields leads to improper chromosome segregation and mitotic catastrophe in cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676010/
https://www.ncbi.nlm.nih.gov/pubmed/26658786
http://dx.doi.org/10.1038/srep18046
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