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Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption
Dysregulation of iron metabolism is a common characteristic of cancer cells. The rapid proliferation of the tumour cells means that there is an increased dependence upon iron compared to healthy cells. Chelation of iron can be undertaken with a number of different compounds, however, simply lowering...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267116/ https://www.ncbi.nlm.nih.gov/pubmed/30506101 http://dx.doi.org/10.1007/s10856-018-6190-x |
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author | Perring, James Crawshay-Williams, Felicity Huang, Cindy Townley, Helen E |
author_facet | Perring, James Crawshay-Williams, Felicity Huang, Cindy Townley, Helen E |
author_sort | Perring, James |
collection | PubMed |
description | Dysregulation of iron metabolism is a common characteristic of cancer cells. The rapid proliferation of the tumour cells means that there is an increased dependence upon iron compared to healthy cells. Chelation of iron can be undertaken with a number of different compounds, however, simply lowering systemic iron levels to control tumour growth is not possible since iron is essential for cellular metabolism in the rest of the body. Nanoparticulate iron chelators could overcome this difficulty by targeting to the tumour either by the passive enhanced permeation and retention effect, or by targeting ligands on the surface. Nanoparticles were prepared from melanin, which is a naturally occurring pigment that is widely distributed within the body, but that can chelate iron. The prepared nanoparticles were shown to be ~220 nm, and could adsorb 16.45 mmoles iron/g melanin. The nanoparticles showed no affect on control fibroblast cells at a concentration of 200 μM, whereas the immortalised cancer cell lines showed at least 56% reduction in cell growth. At a concentration of 1 mM melanin nanoparticles the cell growth could be reduced by 99% compared to the control. The nanoparticles also show no significant haemotoxicity, even at concentration of 500 μM. Melanin nanoparticles are therefore a viable prospect for destroying cancer cells via iron starvation. [Image: see text] |
format | Online Article Text |
id | pubmed-6267116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-62671162018-12-11 Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption Perring, James Crawshay-Williams, Felicity Huang, Cindy Townley, Helen E J Mater Sci Mater Med Engineering and Nano-engineering Approaches for Medical Devices Dysregulation of iron metabolism is a common characteristic of cancer cells. The rapid proliferation of the tumour cells means that there is an increased dependence upon iron compared to healthy cells. Chelation of iron can be undertaken with a number of different compounds, however, simply lowering systemic iron levels to control tumour growth is not possible since iron is essential for cellular metabolism in the rest of the body. Nanoparticulate iron chelators could overcome this difficulty by targeting to the tumour either by the passive enhanced permeation and retention effect, or by targeting ligands on the surface. Nanoparticles were prepared from melanin, which is a naturally occurring pigment that is widely distributed within the body, but that can chelate iron. The prepared nanoparticles were shown to be ~220 nm, and could adsorb 16.45 mmoles iron/g melanin. The nanoparticles showed no affect on control fibroblast cells at a concentration of 200 μM, whereas the immortalised cancer cell lines showed at least 56% reduction in cell growth. At a concentration of 1 mM melanin nanoparticles the cell growth could be reduced by 99% compared to the control. The nanoparticles also show no significant haemotoxicity, even at concentration of 500 μM. Melanin nanoparticles are therefore a viable prospect for destroying cancer cells via iron starvation. [Image: see text] Springer US 2018-11-30 2018 /pmc/articles/PMC6267116/ /pubmed/30506101 http://dx.doi.org/10.1007/s10856-018-6190-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, 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 license, and indicate if changes were made. |
spellingShingle | Engineering and Nano-engineering Approaches for Medical Devices Perring, James Crawshay-Williams, Felicity Huang, Cindy Townley, Helen E Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title | Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title_full | Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title_fullStr | Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title_full_unstemmed | Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title_short | Bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
title_sort | bio-inspired melanin nanoparticles induce cancer cell death by iron adsorption |
topic | Engineering and Nano-engineering Approaches for Medical Devices |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267116/ https://www.ncbi.nlm.nih.gov/pubmed/30506101 http://dx.doi.org/10.1007/s10856-018-6190-x |
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