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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...

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Autores principales: Pedrosa, Pedro, Heuer-Jungemann, Amelie, Kanaras, Antonios G., Fernandes, Alexandra R., Baptista, Pedro V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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