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Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements
Cellular response to non-lethal radiation stress include perturbations in DNA repair, angiogenesis, migration, and adhesion, among others. Low-LET proton beam radiation has been shown to induce somewhat different biological response than photon radiation. For example, we have shown that non-lethal d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504917/ https://www.ncbi.nlm.nih.gov/pubmed/31065009 http://dx.doi.org/10.1038/s41598-019-43453-7 |
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author | Jasińska-Konior, Katarzyna Wiecheć, Olga Sarna, Michał Panek, Agnieszka Swakoń, Jan Michalik, Marta Urbańska, Krystyna Elas, Martyna |
author_facet | Jasińska-Konior, Katarzyna Wiecheć, Olga Sarna, Michał Panek, Agnieszka Swakoń, Jan Michalik, Marta Urbańska, Krystyna Elas, Martyna |
author_sort | Jasińska-Konior, Katarzyna |
collection | PubMed |
description | Cellular response to non-lethal radiation stress include perturbations in DNA repair, angiogenesis, migration, and adhesion, among others. Low-LET proton beam radiation has been shown to induce somewhat different biological response than photon radiation. For example, we have shown that non-lethal doses of proton beam radiation inhibited migration of cells and that this effect persisted long-term. Here, we have examined cellular elasticity and actin cytoskeleton organization in BLM cutaneous melanoma and Mel270 uveal melanoma cells. Proton beam radiation increased cellular elasticity to a greater extent than X-rays and both types of radiation induced changes in actin cytoskeleton organization. Vimentin level increased in BLM cells after both types of radiation. Our data show that cell elasticity increased substantially after low-LET proton beam and persisted long after radiation. This may have significant consequences for the migratory properties of melanoma cells, as well as for the cell susceptibility to therapy. |
format | Online Article Text |
id | pubmed-6504917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65049172019-05-21 Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements Jasińska-Konior, Katarzyna Wiecheć, Olga Sarna, Michał Panek, Agnieszka Swakoń, Jan Michalik, Marta Urbańska, Krystyna Elas, Martyna Sci Rep Article Cellular response to non-lethal radiation stress include perturbations in DNA repair, angiogenesis, migration, and adhesion, among others. Low-LET proton beam radiation has been shown to induce somewhat different biological response than photon radiation. For example, we have shown that non-lethal doses of proton beam radiation inhibited migration of cells and that this effect persisted long-term. Here, we have examined cellular elasticity and actin cytoskeleton organization in BLM cutaneous melanoma and Mel270 uveal melanoma cells. Proton beam radiation increased cellular elasticity to a greater extent than X-rays and both types of radiation induced changes in actin cytoskeleton organization. Vimentin level increased in BLM cells after both types of radiation. Our data show that cell elasticity increased substantially after low-LET proton beam and persisted long after radiation. This may have significant consequences for the migratory properties of melanoma cells, as well as for the cell susceptibility to therapy. Nature Publishing Group UK 2019-05-07 /pmc/articles/PMC6504917/ /pubmed/31065009 http://dx.doi.org/10.1038/s41598-019-43453-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jasińska-Konior, Katarzyna Wiecheć, Olga Sarna, Michał Panek, Agnieszka Swakoń, Jan Michalik, Marta Urbańska, Krystyna Elas, Martyna Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title | Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title_full | Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title_fullStr | Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title_full_unstemmed | Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title_short | Increased elasticity of melanoma cells after low-LET proton beam due to actin cytoskeleton rearrangements |
title_sort | increased elasticity of melanoma cells after low-let proton beam due to actin cytoskeleton rearrangements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6504917/ https://www.ncbi.nlm.nih.gov/pubmed/31065009 http://dx.doi.org/10.1038/s41598-019-43453-7 |
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