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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...

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Autores principales: Jaworski, Sławomir, Biniecka, Paulina, Bugajska, Żaneta, Daniluk, Karolina, Dyjak, Sławomir, Strojny, Barbara, Kutwin, Marta, Wierzbicki, Mateusz, Grodzik, Marta, Chwalibog, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
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.
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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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