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Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer
In the field of oncology research, a deeper understanding of tumor biology has shed light on the role of environmental conditions surrounding cancer cells. In this regard, targeting the tumor microenvironment has recently emerged as a new way to access this disease. In this work, a novel extracellul...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930284/ https://www.ncbi.nlm.nih.gov/pubmed/33658580 http://dx.doi.org/10.1038/s41598-021-84492-3 |
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author | De Vita, Alessandro Liverani, Chiara Molinaro, Roberto Martinez, Jonathan O. Hartman, Kelly A. Spadazzi, Chiara Miserocchi, Giacomo Taraballi, Francesca Evangelopoulos, Michael Pieri, Federica Bongiovanni, Alberto Mercatali, Laura Tasciotti, Ennio Ibrahim, Toni |
author_facet | De Vita, Alessandro Liverani, Chiara Molinaro, Roberto Martinez, Jonathan O. Hartman, Kelly A. Spadazzi, Chiara Miserocchi, Giacomo Taraballi, Francesca Evangelopoulos, Michael Pieri, Federica Bongiovanni, Alberto Mercatali, Laura Tasciotti, Ennio Ibrahim, Toni |
author_sort | De Vita, Alessandro |
collection | PubMed |
description | In the field of oncology research, a deeper understanding of tumor biology has shed light on the role of environmental conditions surrounding cancer cells. In this regard, targeting the tumor microenvironment has recently emerged as a new way to access this disease. In this work, a novel extracellular matrix (ECM)-targeting nanotherapeutic was engineered using a lipid-based nanoparticle chemically linked to an inhibitor of the ECM-related enzyme, lysyl oxidase 1 (LOX), that inhibits the crosslinking of elastin and collagen fibers. We demonstrated that, when the conjugated vesicles were loaded with the chemotherapeutic epirubicin, superior inhibition of triple negative breast cancer (TNBC) cell growth was observed both in vitro and in vivo. Moreover, in vivo results displayed prolonged survival, minimal cytotoxicity, and enhanced biocompatibility compared to free epirubicin and epirubicin-loaded nanoparticles. This all-in-one nano-based ECM-targeting chemotherapeutic may provide a key-enabling technology for the treatment of TNBC. |
format | Online Article Text |
id | pubmed-7930284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79302842021-03-05 Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer De Vita, Alessandro Liverani, Chiara Molinaro, Roberto Martinez, Jonathan O. Hartman, Kelly A. Spadazzi, Chiara Miserocchi, Giacomo Taraballi, Francesca Evangelopoulos, Michael Pieri, Federica Bongiovanni, Alberto Mercatali, Laura Tasciotti, Ennio Ibrahim, Toni Sci Rep Article In the field of oncology research, a deeper understanding of tumor biology has shed light on the role of environmental conditions surrounding cancer cells. In this regard, targeting the tumor microenvironment has recently emerged as a new way to access this disease. In this work, a novel extracellular matrix (ECM)-targeting nanotherapeutic was engineered using a lipid-based nanoparticle chemically linked to an inhibitor of the ECM-related enzyme, lysyl oxidase 1 (LOX), that inhibits the crosslinking of elastin and collagen fibers. We demonstrated that, when the conjugated vesicles were loaded with the chemotherapeutic epirubicin, superior inhibition of triple negative breast cancer (TNBC) cell growth was observed both in vitro and in vivo. Moreover, in vivo results displayed prolonged survival, minimal cytotoxicity, and enhanced biocompatibility compared to free epirubicin and epirubicin-loaded nanoparticles. This all-in-one nano-based ECM-targeting chemotherapeutic may provide a key-enabling technology for the treatment of TNBC. Nature Publishing Group UK 2021-03-03 /pmc/articles/PMC7930284/ /pubmed/33658580 http://dx.doi.org/10.1038/s41598-021-84492-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article De Vita, Alessandro Liverani, Chiara Molinaro, Roberto Martinez, Jonathan O. Hartman, Kelly A. Spadazzi, Chiara Miserocchi, Giacomo Taraballi, Francesca Evangelopoulos, Michael Pieri, Federica Bongiovanni, Alberto Mercatali, Laura Tasciotti, Ennio Ibrahim, Toni Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title | Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title_full | Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title_fullStr | Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title_full_unstemmed | Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title_short | Lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
title_sort | lysyl oxidase engineered lipid nanovesicles for the treatment of triple negative breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930284/ https://www.ncbi.nlm.nih.gov/pubmed/33658580 http://dx.doi.org/10.1038/s41598-021-84492-3 |
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