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Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells
A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m(2)/g, well-developed porosity, and high electric...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441660/ https://www.ncbi.nlm.nih.gov/pubmed/28572728 http://dx.doi.org/10.2147/IJN.S135932 |
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author | Jaworski, Sławomir Biniecka, Paulina Bugajska, Żaneta Daniluk, Karolina Dyjak, Sławomir Strojny, Barbara Kutwin, Marta Wierzbicki, Mateusz Grodzik, Marta Chwalibog, André |
author_facet | Jaworski, Sławomir Biniecka, Paulina Bugajska, Żaneta Daniluk, Karolina Dyjak, Sławomir Strojny, Barbara Kutwin, Marta Wierzbicki, Mateusz Grodzik, Marta Chwalibog, André |
author_sort | Jaworski, Sławomir |
collection | PubMed |
description | A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m(2)/g, well-developed porosity, and high electrical conductivity. These unique properties and ability to transfer charge create a possibility of employing HNC as a moderator of tumor cell growth. As the charge of HNC may interfere with cell membranes by adhesion and by bonding with cell receptors, it may block the supply of nutrients. The interactions of HNC with the U87 cells can also lead to the excessive generation of reactive oxygen species (ROS) and activate apoptotic mechanisms in cancer cells. The investigation was performed using U87 human glioblastoma and PCS-201–010 normal fibroblast cell lines, where cell morphology and ultrastructure, viability, ROS production, type of cell death, mitochondrial transmembrane potential, and the expression of genes engaged in apoptosis pathways are studied. The results demonstrate that cytotoxicity of HNC particles increases with concentration from 5 to 100 µg/mL by activation of apoptosis through the mitochondrial pathway, without inducing necrosis. Our research indicates the potential applicability of HNC in cancer therapy. |
format | Online Article Text |
id | pubmed-5441660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54416602017-06-01 Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells Jaworski, Sławomir Biniecka, Paulina Bugajska, Żaneta Daniluk, Karolina Dyjak, Sławomir Strojny, Barbara Kutwin, Marta Wierzbicki, Mateusz Grodzik, Marta Chwalibog, André Int J Nanomedicine Original Research A newly produced hierarchical, nanoporous carbon (HNC) material is studied for the first time in a biological model. The material consists of uniform particles and is characterized by a mean diameter <150 nm, a high specific surface area of 1,000 m(2)/g, well-developed porosity, and high electrical conductivity. These unique properties and ability to transfer charge create a possibility of employing HNC as a moderator of tumor cell growth. As the charge of HNC may interfere with cell membranes by adhesion and by bonding with cell receptors, it may block the supply of nutrients. The interactions of HNC with the U87 cells can also lead to the excessive generation of reactive oxygen species (ROS) and activate apoptotic mechanisms in cancer cells. The investigation was performed using U87 human glioblastoma and PCS-201–010 normal fibroblast cell lines, where cell morphology and ultrastructure, viability, ROS production, type of cell death, mitochondrial transmembrane potential, and the expression of genes engaged in apoptosis pathways are studied. The results demonstrate that cytotoxicity of HNC particles increases with concentration from 5 to 100 µg/mL by activation of apoptosis through the mitochondrial pathway, without inducing necrosis. Our research indicates the potential applicability of HNC in cancer therapy. Dove Medical Press 2017-05-18 /pmc/articles/PMC5441660/ /pubmed/28572728 http://dx.doi.org/10.2147/IJN.S135932 Text en © 2017 Jaworski et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Jaworski, Sławomir Biniecka, Paulina Bugajska, Żaneta Daniluk, Karolina Dyjak, Sławomir Strojny, Barbara Kutwin, Marta Wierzbicki, Mateusz Grodzik, Marta Chwalibog, André Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title | Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title_full | Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title_fullStr | Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title_full_unstemmed | Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title_short | Analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade IV cells |
title_sort | analysis of the cytotoxicity of hierarchical nanoporous graphenic carbon against human glioblastoma grade iv cells |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441660/ https://www.ncbi.nlm.nih.gov/pubmed/28572728 http://dx.doi.org/10.2147/IJN.S135932 |
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