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Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach

Tumors are complex tissues that consist of stromal cells, such as fibroblasts, immune cells and mesenchymal stem cells, as well as non-cellular components, in addition to neoplastic cells. Increasingly, there is evidence to suggest that these non-neoplastic cell components support cancer initiation,...

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Detalles Bibliográficos
Autores principales: Adjei, Isaac M., Blanka, Sharma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384103/
https://www.ncbi.nlm.nih.gov/pubmed/25695337
http://dx.doi.org/10.3390/jfb6010081
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author Adjei, Isaac M.
Blanka, Sharma
author_facet Adjei, Isaac M.
Blanka, Sharma
author_sort Adjei, Isaac M.
collection PubMed
description Tumors are complex tissues that consist of stromal cells, such as fibroblasts, immune cells and mesenchymal stem cells, as well as non-cellular components, in addition to neoplastic cells. Increasingly, there is evidence to suggest that these non-neoplastic cell components support cancer initiation, progression and metastasis and that their ablation or reprogramming can inhibit tumor growth. Our understanding of the activities of different parts of the tumor stroma in advancing cancer has been improved by the use of scaffold and matrix-based 3D systems originally developed for regenerative medicine. Additionally, drug delivery systems made from synthetic and natural biomaterials deliver drugs to kill stromal cells or reprogram the microenvironment for tumor inhibition. In this article, we review the impact of 3D tumor models in increasing our understanding of tumorigenesis. We also discuss how different drug delivery systems aid in the reprogramming of tumor stroma for cancer treatment.
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spelling pubmed-43841032015-05-05 Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach Adjei, Isaac M. Blanka, Sharma J Funct Biomater Review Tumors are complex tissues that consist of stromal cells, such as fibroblasts, immune cells and mesenchymal stem cells, as well as non-cellular components, in addition to neoplastic cells. Increasingly, there is evidence to suggest that these non-neoplastic cell components support cancer initiation, progression and metastasis and that their ablation or reprogramming can inhibit tumor growth. Our understanding of the activities of different parts of the tumor stroma in advancing cancer has been improved by the use of scaffold and matrix-based 3D systems originally developed for regenerative medicine. Additionally, drug delivery systems made from synthetic and natural biomaterials deliver drugs to kill stromal cells or reprogram the microenvironment for tumor inhibition. In this article, we review the impact of 3D tumor models in increasing our understanding of tumorigenesis. We also discuss how different drug delivery systems aid in the reprogramming of tumor stroma for cancer treatment. MDPI 2015-02-17 /pmc/articles/PMC4384103/ /pubmed/25695337 http://dx.doi.org/10.3390/jfb6010081 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Adjei, Isaac M.
Blanka, Sharma
Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title_full Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title_fullStr Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title_full_unstemmed Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title_short Modulation of the Tumor Microenvironment for Cancer Treatment: A Biomaterials Approach
title_sort modulation of the tumor microenvironment for cancer treatment: a biomaterials approach
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384103/
https://www.ncbi.nlm.nih.gov/pubmed/25695337
http://dx.doi.org/10.3390/jfb6010081
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