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An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy

DNA origami systems could be important candidates for clinical applications. Unfortunately, their intrinsic properties such as the activation of non-specific immune system responses leading to inflammation, instability in physiological solutions, and a short in vivo lifetime are the major challenges...

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Autores principales: Palazzolo, Stefano, Hadla, Mohamad, Russo Spena, Concetta, Caligiuri, Isabella, Rotondo, Rossella, Adeel, Muhammad, Kumar, Vinit, Corona, Giuseppe, Canzonieri, Vincenzo, Toffoli, Giuseppe, Rizzolio, Flavio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966502/
https://www.ncbi.nlm.nih.gov/pubmed/31842277
http://dx.doi.org/10.3390/cancers11121997
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author Palazzolo, Stefano
Hadla, Mohamad
Russo Spena, Concetta
Caligiuri, Isabella
Rotondo, Rossella
Adeel, Muhammad
Kumar, Vinit
Corona, Giuseppe
Canzonieri, Vincenzo
Toffoli, Giuseppe
Rizzolio, Flavio
author_facet Palazzolo, Stefano
Hadla, Mohamad
Russo Spena, Concetta
Caligiuri, Isabella
Rotondo, Rossella
Adeel, Muhammad
Kumar, Vinit
Corona, Giuseppe
Canzonieri, Vincenzo
Toffoli, Giuseppe
Rizzolio, Flavio
author_sort Palazzolo, Stefano
collection PubMed
description DNA origami systems could be important candidates for clinical applications. Unfortunately, their intrinsic properties such as the activation of non-specific immune system responses leading to inflammation, instability in physiological solutions, and a short in vivo lifetime are the major challenges for real world applications. A compact short tube DNA origami (STDO) of 30 nm in length and 10 nm in width was designed to fit inside the core of a stealth liposome (LSTDO) of about 150 nm to remote load doxorubicin. Biocompatibility was tested in three-dimensional (3D) organoid cultures and in vivo. Efficacy was evaluated in different cell lines and in a xenograft breast cancer mouse model. As described in a previous work, LSTDO is highly stable and biocompatible, escaping the recognition of the immune system. Here we show that LSTDO have an increased toleration in mouse liver organoids used as an ex vivo model that recapitulate the tissue of origin. This innovative drug delivery system (DDS) improves the antitumoral efficacy and biodistribution of doxorubicin in tumor-bearing mice and decreases bone marrow toxicity. Our application is an attractive system for the remote loading of other drugs able to interact with DNA for the preparation of liposomal formulations.
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spelling pubmed-69665022020-01-27 An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy Palazzolo, Stefano Hadla, Mohamad Russo Spena, Concetta Caligiuri, Isabella Rotondo, Rossella Adeel, Muhammad Kumar, Vinit Corona, Giuseppe Canzonieri, Vincenzo Toffoli, Giuseppe Rizzolio, Flavio Cancers (Basel) Article DNA origami systems could be important candidates for clinical applications. Unfortunately, their intrinsic properties such as the activation of non-specific immune system responses leading to inflammation, instability in physiological solutions, and a short in vivo lifetime are the major challenges for real world applications. A compact short tube DNA origami (STDO) of 30 nm in length and 10 nm in width was designed to fit inside the core of a stealth liposome (LSTDO) of about 150 nm to remote load doxorubicin. Biocompatibility was tested in three-dimensional (3D) organoid cultures and in vivo. Efficacy was evaluated in different cell lines and in a xenograft breast cancer mouse model. As described in a previous work, LSTDO is highly stable and biocompatible, escaping the recognition of the immune system. Here we show that LSTDO have an increased toleration in mouse liver organoids used as an ex vivo model that recapitulate the tissue of origin. This innovative drug delivery system (DDS) improves the antitumoral efficacy and biodistribution of doxorubicin in tumor-bearing mice and decreases bone marrow toxicity. Our application is an attractive system for the remote loading of other drugs able to interact with DNA for the preparation of liposomal formulations. MDPI 2019-12-12 /pmc/articles/PMC6966502/ /pubmed/31842277 http://dx.doi.org/10.3390/cancers11121997 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Palazzolo, Stefano
Hadla, Mohamad
Russo Spena, Concetta
Caligiuri, Isabella
Rotondo, Rossella
Adeel, Muhammad
Kumar, Vinit
Corona, Giuseppe
Canzonieri, Vincenzo
Toffoli, Giuseppe
Rizzolio, Flavio
An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title_full An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title_fullStr An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title_full_unstemmed An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title_short An Effective Multi-Stage Liposomal DNA Origami Nanosystem for In Vivo Cancer Therapy
title_sort effective multi-stage liposomal dna origami nanosystem for in vivo cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966502/
https://www.ncbi.nlm.nih.gov/pubmed/31842277
http://dx.doi.org/10.3390/cancers11121997
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