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Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin

One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offe...

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Autores principales: Han, Ocean, Bromma, Kyle, Palmerley, Nicholas, Bido, Ariadne T., Monica, Mesa, Alhussan, Abdulaziz, Howard, Perry L., Brolo, Alexandre G., Beckham, Wayne, Alexander, Abraham S., Chithrani, Devika B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875790/
https://www.ncbi.nlm.nih.gov/pubmed/35213967
http://dx.doi.org/10.3390/pharmaceutics14020233
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author Han, Ocean
Bromma, Kyle
Palmerley, Nicholas
Bido, Ariadne T.
Monica, Mesa
Alhussan, Abdulaziz
Howard, Perry L.
Brolo, Alexandre G.
Beckham, Wayne
Alexander, Abraham S.
Chithrani, Devika B.
author_facet Han, Ocean
Bromma, Kyle
Palmerley, Nicholas
Bido, Ariadne T.
Monica, Mesa
Alhussan, Abdulaziz
Howard, Perry L.
Brolo, Alexandre G.
Beckham, Wayne
Alexander, Abraham S.
Chithrani, Devika B.
author_sort Han, Ocean
collection PubMed
description One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offer a two-fold promise as a delivery vehicle for BLM and as a radiosensitizing agent. In this study, GNPs were functionalized and complexed with BLM using a gold-thiol bond (denoted GNP-BLM). Our results show that there was a 40% and 10% decrease in cell growth with GNP-BLM vs. free BLM for the MIA PaCa-2 and PC-3 cell lines, respectively. Testing the GNP-BLM platform with RT showed an 84% and 13% reduction in cell growth in MIA PaCa-2 cells treated with GNP-BLM and GNPs, respectively. Similar results were seen with PC-3 cells. The efficacy of this approach was verified by mapping DNA double-strand breaks (DSBs) as well. Therefore, this proposed incorporation of nanomedicine with RT is promising in achieving a significantly higher therapeutic ratio which is necessary to make a paradigm change to the current clinical approach.
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spelling pubmed-88757902022-02-26 Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin Han, Ocean Bromma, Kyle Palmerley, Nicholas Bido, Ariadne T. Monica, Mesa Alhussan, Abdulaziz Howard, Perry L. Brolo, Alexandre G. Beckham, Wayne Alexander, Abraham S. Chithrani, Devika B. Pharmaceutics Article One of the major issues in current radiotherapy (RT) is the associated normal tissue toxicity. Enhancement of the RT effect with novel radiosensitizers can address this need. In this study, gold nanoparticles (GNPs) and bleomycin (BLM) were used as a unique combination of radiosensitizers. GNPs offer a two-fold promise as a delivery vehicle for BLM and as a radiosensitizing agent. In this study, GNPs were functionalized and complexed with BLM using a gold-thiol bond (denoted GNP-BLM). Our results show that there was a 40% and 10% decrease in cell growth with GNP-BLM vs. free BLM for the MIA PaCa-2 and PC-3 cell lines, respectively. Testing the GNP-BLM platform with RT showed an 84% and 13% reduction in cell growth in MIA PaCa-2 cells treated with GNP-BLM and GNPs, respectively. Similar results were seen with PC-3 cells. The efficacy of this approach was verified by mapping DNA double-strand breaks (DSBs) as well. Therefore, this proposed incorporation of nanomedicine with RT is promising in achieving a significantly higher therapeutic ratio which is necessary to make a paradigm change to the current clinical approach. MDPI 2022-01-20 /pmc/articles/PMC8875790/ /pubmed/35213967 http://dx.doi.org/10.3390/pharmaceutics14020233 Text en © 2022 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 Article
Han, Ocean
Bromma, Kyle
Palmerley, Nicholas
Bido, Ariadne T.
Monica, Mesa
Alhussan, Abdulaziz
Howard, Perry L.
Brolo, Alexandre G.
Beckham, Wayne
Alexander, Abraham S.
Chithrani, Devika B.
Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title_full Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title_fullStr Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title_full_unstemmed Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title_short Nanotechnology Driven Cancer Chemoradiation: Exploiting the Full Potential of Radiotherapy with a Unique Combination of Gold Nanoparticles and Bleomycin
title_sort nanotechnology driven cancer chemoradiation: exploiting the full potential of radiotherapy with a unique combination of gold nanoparticles and bleomycin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875790/
https://www.ncbi.nlm.nih.gov/pubmed/35213967
http://dx.doi.org/10.3390/pharmaceutics14020233
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