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Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure

The use of alpha-particle (α-particle) radionuclides, especially [(223)Ra]RaCl(2) (radium dichloride), for targeted alpha therapy is steadily increasing. Despite the positive clinical outcomes of this therapy, very little data are available about the effect on the ultrastructure of cells. The purpos...

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Autores principales: Diniz Filho, Joel Félix Silva, de Barros, Aline Oliveira da Silva, Pijeira, Martha Sahylí Ortega, Ricci-Junior, Eduardo, Midlej, Victor, Baroni, Mariana Pelissari Monteiro Aguiar, dos Santos, Clenilton Costa, Alencar, Luciana Magalhães Rebelo, Santos-Oliveira, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913731/
https://www.ncbi.nlm.nih.gov/pubmed/36766793
http://dx.doi.org/10.3390/cells12030451
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author Diniz Filho, Joel Félix Silva
de Barros, Aline Oliveira da Silva
Pijeira, Martha Sahylí Ortega
Ricci-Junior, Eduardo
Midlej, Victor
Baroni, Mariana Pelissari Monteiro Aguiar
dos Santos, Clenilton Costa
Alencar, Luciana Magalhães Rebelo
Santos-Oliveira, Ralph
author_facet Diniz Filho, Joel Félix Silva
de Barros, Aline Oliveira da Silva
Pijeira, Martha Sahylí Ortega
Ricci-Junior, Eduardo
Midlej, Victor
Baroni, Mariana Pelissari Monteiro Aguiar
dos Santos, Clenilton Costa
Alencar, Luciana Magalhães Rebelo
Santos-Oliveira, Ralph
author_sort Diniz Filho, Joel Félix Silva
collection PubMed
description The use of alpha-particle (α-particle) radionuclides, especially [(223)Ra]RaCl(2) (radium dichloride), for targeted alpha therapy is steadily increasing. Despite the positive clinical outcomes of this therapy, very little data are available about the effect on the ultrastructure of cells. The purpose of this study was to evaluate the nanomechanical and ultrastructure effect of [(223)Ra] RaCl(2) on cancer cells. To analyze the effect of [(223)Ra]RaCl(2) on tumor cells, human breast cancer cells (lineage MDA-MB-231) were cultured and treated with the radiopharmaceutical at doses of 2 µCi and 0.9 µCi. The effect was evaluated using atomic force microscopy (AFM) and transmission electron microscopy (TEM) combined with Raman spectroscopy. The results showed massive destruction of the cell membrane but preservation of the nucleus membrane. No evidence of DNA alteration was observed. The data demonstrated the formation of lysosomes and phagosomes. These findings help elucidate the main mechanism involved in cell death during α-particle therapy.
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spelling pubmed-99137312023-02-11 Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure Diniz Filho, Joel Félix Silva de Barros, Aline Oliveira da Silva Pijeira, Martha Sahylí Ortega Ricci-Junior, Eduardo Midlej, Victor Baroni, Mariana Pelissari Monteiro Aguiar dos Santos, Clenilton Costa Alencar, Luciana Magalhães Rebelo Santos-Oliveira, Ralph Cells Communication The use of alpha-particle (α-particle) radionuclides, especially [(223)Ra]RaCl(2) (radium dichloride), for targeted alpha therapy is steadily increasing. Despite the positive clinical outcomes of this therapy, very little data are available about the effect on the ultrastructure of cells. The purpose of this study was to evaluate the nanomechanical and ultrastructure effect of [(223)Ra] RaCl(2) on cancer cells. To analyze the effect of [(223)Ra]RaCl(2) on tumor cells, human breast cancer cells (lineage MDA-MB-231) were cultured and treated with the radiopharmaceutical at doses of 2 µCi and 0.9 µCi. The effect was evaluated using atomic force microscopy (AFM) and transmission electron microscopy (TEM) combined with Raman spectroscopy. The results showed massive destruction of the cell membrane but preservation of the nucleus membrane. No evidence of DNA alteration was observed. The data demonstrated the formation of lysosomes and phagosomes. These findings help elucidate the main mechanism involved in cell death during α-particle therapy. MDPI 2023-01-31 /pmc/articles/PMC9913731/ /pubmed/36766793 http://dx.doi.org/10.3390/cells12030451 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Diniz Filho, Joel Félix Silva
de Barros, Aline Oliveira da Silva
Pijeira, Martha Sahylí Ortega
Ricci-Junior, Eduardo
Midlej, Victor
Baroni, Mariana Pelissari Monteiro Aguiar
dos Santos, Clenilton Costa
Alencar, Luciana Magalhães Rebelo
Santos-Oliveira, Ralph
Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title_full Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title_fullStr Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title_full_unstemmed Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title_short Ultrastructural Analysis of Cancer Cells Treated with the Radiopharmaceutical Radium Dichloride ([(223)Ra]RaCl(2)): Understanding the Effect on Cell Structure
title_sort ultrastructural analysis of cancer cells treated with the radiopharmaceutical radium dichloride ([(223)ra]racl(2)): understanding the effect on cell structure
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913731/
https://www.ncbi.nlm.nih.gov/pubmed/36766793
http://dx.doi.org/10.3390/cells12030451
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