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Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles
BACKGROUND: Anti-angiogenic therapy has great potential for cancer therapy with several FDA approved formulations but there are considerable side effects upon the normal blood vessels that decrease the potential application of such therapeutics. Chicken chorioallantoic membrane (CAM) has been used a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697398/ https://www.ncbi.nlm.nih.gov/pubmed/29162137 http://dx.doi.org/10.1186/s12951-017-0321-2 |
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author | Pedrosa, Pedro Heuer-Jungemann, Amelie Kanaras, Antonios G. Fernandes, Alexandra R. Baptista, Pedro V. |
author_facet | Pedrosa, Pedro Heuer-Jungemann, Amelie Kanaras, Antonios G. Fernandes, Alexandra R. Baptista, Pedro V. |
author_sort | Pedrosa, Pedro |
collection | PubMed |
description | BACKGROUND: Anti-angiogenic therapy has great potential for cancer therapy with several FDA approved formulations but there are considerable side effects upon the normal blood vessels that decrease the potential application of such therapeutics. Chicken chorioallantoic membrane (CAM) has been used as a model to study angiogenesis in vivo. Using a CAM model, it had been previously shown that spherical gold nanoparticles functionalised with an anti-angiogenic peptide can humper neo-angiogenesis. RESULTS: Our results show that gold nanoparticles conjugated with an anti-angiogenic peptide can be combined with visible laser irradiation to enhance angiogenesis arrest in vivo. We show that a green laser coupled to gold nanoparticles can achieve high localized temperatures able to precisely cauterize blood vessels. This combined therapy acts via VEGFR pathway inhibition, leading to a fourfold reduction in FLT-1 expression. CONCLUSIONS: The proposed phototherapy extends the use of visible lasers in clinics, combining it with chemotherapy to potentiate cancer treatment. This approach allows the reduction of dose of anti-angiogenic peptide, thus reducing possible side effects, while destroying blood vessels supply critical for tumour progression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-017-0321-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5697398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56973982017-12-01 Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles Pedrosa, Pedro Heuer-Jungemann, Amelie Kanaras, Antonios G. Fernandes, Alexandra R. Baptista, Pedro V. J Nanobiotechnology Research BACKGROUND: Anti-angiogenic therapy has great potential for cancer therapy with several FDA approved formulations but there are considerable side effects upon the normal blood vessels that decrease the potential application of such therapeutics. Chicken chorioallantoic membrane (CAM) has been used as a model to study angiogenesis in vivo. Using a CAM model, it had been previously shown that spherical gold nanoparticles functionalised with an anti-angiogenic peptide can humper neo-angiogenesis. RESULTS: Our results show that gold nanoparticles conjugated with an anti-angiogenic peptide can be combined with visible laser irradiation to enhance angiogenesis arrest in vivo. We show that a green laser coupled to gold nanoparticles can achieve high localized temperatures able to precisely cauterize blood vessels. This combined therapy acts via VEGFR pathway inhibition, leading to a fourfold reduction in FLT-1 expression. CONCLUSIONS: The proposed phototherapy extends the use of visible lasers in clinics, combining it with chemotherapy to potentiate cancer treatment. This approach allows the reduction of dose of anti-angiogenic peptide, thus reducing possible side effects, while destroying blood vessels supply critical for tumour progression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-017-0321-2) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-21 /pmc/articles/PMC5697398/ /pubmed/29162137 http://dx.doi.org/10.1186/s12951-017-0321-2 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Pedrosa, Pedro Heuer-Jungemann, Amelie Kanaras, Antonios G. Fernandes, Alexandra R. Baptista, Pedro V. Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title | Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title_full | Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title_fullStr | Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title_full_unstemmed | Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title_short | Potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
title_sort | potentiating angiogenesis arrest in vivo via laser irradiation of peptide functionalised gold nanoparticles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697398/ https://www.ncbi.nlm.nih.gov/pubmed/29162137 http://dx.doi.org/10.1186/s12951-017-0321-2 |
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