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A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation

Radiation therapy with heavy particles including neutrons, an otherwise therapeutically perspective because of its high tissue penetration and efficient tumor damage, is currently limited by the lack of adequate equipment. An NG-24 generator (140 kg, 42 × 110 cm, ~1011 particles/s, > 14 MeV) has...

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Autores principales: Yurkov, D. I., Syromukov, S. V., Tatarskiy, V. V., Ivanova, E. S., Khamidullina, A. I., Yastrebova, M. A., Sysoev, V. I., Dobrov, R. V., Belousov, A. V., Morozov, V. N., Kolyvanova, M. A., Krusanov, G. A., Zverev, V. I., Shtil, A. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826147/
https://www.ncbi.nlm.nih.gov/pubmed/31720022
http://dx.doi.org/10.32607/20758251-2019-11-3-99-102
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author Yurkov, D. I.
Syromukov, S. V.
Tatarskiy, V. V.
Ivanova, E. S.
Khamidullina, A. I.
Yastrebova, M. A.
Sysoev, V. I.
Dobrov, R. V.
Belousov, A. V.
Morozov, V. N.
Kolyvanova, M. A.
Krusanov, G. A.
Zverev, V. I.
Shtil, A. A.
author_facet Yurkov, D. I.
Syromukov, S. V.
Tatarskiy, V. V.
Ivanova, E. S.
Khamidullina, A. I.
Yastrebova, M. A.
Sysoev, V. I.
Dobrov, R. V.
Belousov, A. V.
Morozov, V. N.
Kolyvanova, M. A.
Krusanov, G. A.
Zverev, V. I.
Shtil, A. A.
author_sort Yurkov, D. I.
collection PubMed
description Radiation therapy with heavy particles including neutrons, an otherwise therapeutically perspective because of its high tissue penetration and efficient tumor damage, is currently limited by the lack of adequate equipment. An NG-24 generator (140 kg, 42 × 110 cm, ~1011 particles/s, > 14 MeV) has been designed and engineered to replace the huge and environmentally harmful neutron reactors, cyclotrons, and accelerators with a compact, portable, safe, and potent source of high-energy neutrons. We demonstrate that the neutron beam produced by NG-24 causes a significant antiproliferative effect on human tumor cell lines regardless of the status of the anti-apoptotic p53 protein. Phosphorylation of histone 2A and increased amounts of p21, cyclin D, and phospho-p53 were detectable in HCT116 colon carcinoma cells (wild-type p53) irradiated with 4 Gy several days post-treatment, accompanied by G2/M phase arrest. These treatments dramatically reduced the ability of single cells to form colonies. In the HCT116p53KO subline (p53 -/-), the G2/M arrest was independent of the aforementioned mechanisms. Hence, the NG-24 generator is a source of a powerful, therapeutically relevant neutron flux that triggers a p53-independent antiproliferative response in tumor cells.
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spelling pubmed-68261472019-11-12 A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation Yurkov, D. I. Syromukov, S. V. Tatarskiy, V. V. Ivanova, E. S. Khamidullina, A. I. Yastrebova, M. A. Sysoev, V. I. Dobrov, R. V. Belousov, A. V. Morozov, V. N. Kolyvanova, M. A. Krusanov, G. A. Zverev, V. I. Shtil, A. A. Acta Naturae Research Article Radiation therapy with heavy particles including neutrons, an otherwise therapeutically perspective because of its high tissue penetration and efficient tumor damage, is currently limited by the lack of adequate equipment. An NG-24 generator (140 kg, 42 × 110 cm, ~1011 particles/s, > 14 MeV) has been designed and engineered to replace the huge and environmentally harmful neutron reactors, cyclotrons, and accelerators with a compact, portable, safe, and potent source of high-energy neutrons. We demonstrate that the neutron beam produced by NG-24 causes a significant antiproliferative effect on human tumor cell lines regardless of the status of the anti-apoptotic p53 protein. Phosphorylation of histone 2A and increased amounts of p21, cyclin D, and phospho-p53 were detectable in HCT116 colon carcinoma cells (wild-type p53) irradiated with 4 Gy several days post-treatment, accompanied by G2/M phase arrest. These treatments dramatically reduced the ability of single cells to form colonies. In the HCT116p53KO subline (p53 -/-), the G2/M arrest was independent of the aforementioned mechanisms. Hence, the NG-24 generator is a source of a powerful, therapeutically relevant neutron flux that triggers a p53-independent antiproliferative response in tumor cells. A.I. Gordeyev 2019 /pmc/articles/PMC6826147/ /pubmed/31720022 http://dx.doi.org/10.32607/20758251-2019-11-3-99-102 Text en Copyright ® 2019 National Research University Higher School of Economics. http://creativecommons.org/licenses/by/2.0/ 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 work is properly cited.
spellingShingle Research Article
Yurkov, D. I.
Syromukov, S. V.
Tatarskiy, V. V.
Ivanova, E. S.
Khamidullina, A. I.
Yastrebova, M. A.
Sysoev, V. I.
Dobrov, R. V.
Belousov, A. V.
Morozov, V. N.
Kolyvanova, M. A.
Krusanov, G. A.
Zverev, V. I.
Shtil, A. A.
A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title_full A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title_fullStr A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title_full_unstemmed A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title_short A Unique Prototypic Device for Radiation Therapy: The p53-Independent Antiproliferative Effect of Neutron Radiation
title_sort unique prototypic device for radiation therapy: the p53-independent antiproliferative effect of neutron radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826147/
https://www.ncbi.nlm.nih.gov/pubmed/31720022
http://dx.doi.org/10.32607/20758251-2019-11-3-99-102
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