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Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery
Mesenchymal stromal cells are a population of undifferentiated multipotent adult cells possessing extensive self-renewal properties and the potential to differentiate into a variety of mesenchymal lineage cells. They express broad anti-inflammatory and immunomodulatory activity on the immune system...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750611/ https://www.ncbi.nlm.nih.gov/pubmed/29168760 http://dx.doi.org/10.3390/medicines4040087 |
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author | Petrella, Francesco Rimoldi, Isabella Rizzo, Stefania Spaggiari, Lorenzo |
author_facet | Petrella, Francesco Rimoldi, Isabella Rizzo, Stefania Spaggiari, Lorenzo |
author_sort | Petrella, Francesco |
collection | PubMed |
description | Mesenchymal stromal cells are a population of undifferentiated multipotent adult cells possessing extensive self-renewal properties and the potential to differentiate into a variety of mesenchymal lineage cells. They express broad anti-inflammatory and immunomodulatory activity on the immune system and after transplantation can interact with the surrounding microenvironment, promoting tissue healing and regeneration. For this reason, mesenchymal stromal cells have been widely used in regenerative medicine, both in preclinical and clinical settings. Another clinical application of mesenchymal stromal cells is the targeted delivery of chemotherapeutic agents to neoplastic cells, maximizing the cytotoxic activity against cancer cells and minimizing collateral damage to non-neoplastic tissues. Mesenchymal stem cells are home to the stroma of several primary and metastatic neoplasms and hence can be used as vectors for targeted delivery of antineoplastic drugs to the tumour microenvironment, thereby reducing systemic toxicity and maximizing antitumour effects. Paclitaxel and gemcitabine are the chemotherapeutic drugs best loaded by mesenchymal stromal cells and delivered to neoplastic cells, whereas other agents, like pemetrexed, are not internalized by mesenchymal stromal cells and therefore are not suitable for advanced antineoplastic therapy. This review focuses on the state of the art of advanced antineoplastic cell therapy and its future perspectives, emphasizing in vitro and in vivo preclinical results and future clinical applications. |
format | Online Article Text |
id | pubmed-5750611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-57506112018-01-08 Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery Petrella, Francesco Rimoldi, Isabella Rizzo, Stefania Spaggiari, Lorenzo Medicines (Basel) Review Mesenchymal stromal cells are a population of undifferentiated multipotent adult cells possessing extensive self-renewal properties and the potential to differentiate into a variety of mesenchymal lineage cells. They express broad anti-inflammatory and immunomodulatory activity on the immune system and after transplantation can interact with the surrounding microenvironment, promoting tissue healing and regeneration. For this reason, mesenchymal stromal cells have been widely used in regenerative medicine, both in preclinical and clinical settings. Another clinical application of mesenchymal stromal cells is the targeted delivery of chemotherapeutic agents to neoplastic cells, maximizing the cytotoxic activity against cancer cells and minimizing collateral damage to non-neoplastic tissues. Mesenchymal stem cells are home to the stroma of several primary and metastatic neoplasms and hence can be used as vectors for targeted delivery of antineoplastic drugs to the tumour microenvironment, thereby reducing systemic toxicity and maximizing antitumour effects. Paclitaxel and gemcitabine are the chemotherapeutic drugs best loaded by mesenchymal stromal cells and delivered to neoplastic cells, whereas other agents, like pemetrexed, are not internalized by mesenchymal stromal cells and therefore are not suitable for advanced antineoplastic therapy. This review focuses on the state of the art of advanced antineoplastic cell therapy and its future perspectives, emphasizing in vitro and in vivo preclinical results and future clinical applications. MDPI 2017-11-23 /pmc/articles/PMC5750611/ /pubmed/29168760 http://dx.doi.org/10.3390/medicines4040087 Text en © 2017 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 | Review Petrella, Francesco Rimoldi, Isabella Rizzo, Stefania Spaggiari, Lorenzo Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title | Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title_full | Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title_fullStr | Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title_full_unstemmed | Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title_short | Mesenchymal Stromal Cells for Antineoplastic Drug Loading and Delivery |
title_sort | mesenchymal stromal cells for antineoplastic drug loading and delivery |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5750611/ https://www.ncbi.nlm.nih.gov/pubmed/29168760 http://dx.doi.org/10.3390/medicines4040087 |
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