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Platinum nanoparticles: an exquisite tool to overcome radioresistance
BACKGROUD: Small metallic nanoparticles are proposed as potential nanodrugs to optimize the performances of radiotherapy. This strategy, based on the enrichment of tumours with nanoparticles to amplify radiation effects in the tumour, aims at increasing the cytopathic effect in tumours while healthy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506239/ https://www.ncbi.nlm.nih.gov/pubmed/28757899 http://dx.doi.org/10.1186/s12645-017-0028-y |
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author | Li, Sha Porcel, Erika Remita, Hynd Marco, Sergio Réfrégiers, Matthieu Dutertre, Murielle Confalonieri, Fabrice Lacombe, Sandrine |
author_facet | Li, Sha Porcel, Erika Remita, Hynd Marco, Sergio Réfrégiers, Matthieu Dutertre, Murielle Confalonieri, Fabrice Lacombe, Sandrine |
author_sort | Li, Sha |
collection | PubMed |
description | BACKGROUD: Small metallic nanoparticles are proposed as potential nanodrugs to optimize the performances of radiotherapy. This strategy, based on the enrichment of tumours with nanoparticles to amplify radiation effects in the tumour, aims at increasing the cytopathic effect in tumours while healthy tissue is preserved, an important challenge in radiotherapy. Another major cause of radiotherapy failure is the radioresistance of certain cancers. Surprisingly, the use of nanoparticles to overcome radioresistance has not, to the best of our knowledge, been extensively investigated. The mechanisms of radioresistance have been extensively studied using Deinococcus radiodurans, the most radioresistant organism ever reported, as a model. METHODS: In this work, we investigated the impact of ultra-small platinum nanoparticles (1.7 nm) on this organism, including uptake, toxicity, and effects on radiation responses. RESULTS: We showed that the nanoparticles penetrate D. radiodurans cells, despite the 150 nm cell wall thickness with a minimal inhibition concentration on the order of 4.8 mg L(−1). We also found that the nanoparticles amplify gamma ray radiation effects by >40%. CONCLUSIONS: Finally, this study demonstrates the capacity of metallic nanoparticles to amplify radiation in radioresistant organisms, thus opening the perspective to use nanoparticles not only to improve tumour targeting but also to overcome radioresistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12645-017-0028-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5506239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-55062392017-07-27 Platinum nanoparticles: an exquisite tool to overcome radioresistance Li, Sha Porcel, Erika Remita, Hynd Marco, Sergio Réfrégiers, Matthieu Dutertre, Murielle Confalonieri, Fabrice Lacombe, Sandrine Cancer Nanotechnol Research BACKGROUD: Small metallic nanoparticles are proposed as potential nanodrugs to optimize the performances of radiotherapy. This strategy, based on the enrichment of tumours with nanoparticles to amplify radiation effects in the tumour, aims at increasing the cytopathic effect in tumours while healthy tissue is preserved, an important challenge in radiotherapy. Another major cause of radiotherapy failure is the radioresistance of certain cancers. Surprisingly, the use of nanoparticles to overcome radioresistance has not, to the best of our knowledge, been extensively investigated. The mechanisms of radioresistance have been extensively studied using Deinococcus radiodurans, the most radioresistant organism ever reported, as a model. METHODS: In this work, we investigated the impact of ultra-small platinum nanoparticles (1.7 nm) on this organism, including uptake, toxicity, and effects on radiation responses. RESULTS: We showed that the nanoparticles penetrate D. radiodurans cells, despite the 150 nm cell wall thickness with a minimal inhibition concentration on the order of 4.8 mg L(−1). We also found that the nanoparticles amplify gamma ray radiation effects by >40%. CONCLUSIONS: Finally, this study demonstrates the capacity of metallic nanoparticles to amplify radiation in radioresistant organisms, thus opening the perspective to use nanoparticles not only to improve tumour targeting but also to overcome radioresistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12645-017-0028-y) contains supplementary material, which is available to authorized users. Springer Vienna 2017-07-11 2017 /pmc/articles/PMC5506239/ /pubmed/28757899 http://dx.doi.org/10.1186/s12645-017-0028-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Research Li, Sha Porcel, Erika Remita, Hynd Marco, Sergio Réfrégiers, Matthieu Dutertre, Murielle Confalonieri, Fabrice Lacombe, Sandrine Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title | Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title_full | Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title_fullStr | Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title_full_unstemmed | Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title_short | Platinum nanoparticles: an exquisite tool to overcome radioresistance |
title_sort | platinum nanoparticles: an exquisite tool to overcome radioresistance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506239/ https://www.ncbi.nlm.nih.gov/pubmed/28757899 http://dx.doi.org/10.1186/s12645-017-0028-y |
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