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Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity
Tumor microenvironment has been recognized as a key determinant of tumor formation and metastasis, but how tumor microenvironment is affected by nanomaterials is essentially unknown. Here, we investigated whether carbon nanotubes (CNTs), a widely used nanomaterial with known carcinogenic potential,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172236/ https://www.ncbi.nlm.nih.gov/pubmed/27996035 http://dx.doi.org/10.1038/srep39558 |
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author | Luanpitpong, Sudjit Wang, Liying Castranova, Vincent Dinu, Cerasela Zoica Issaragrisil, Surapol Chen, Yi Charlie Rojanasakul, Yon |
author_facet | Luanpitpong, Sudjit Wang, Liying Castranova, Vincent Dinu, Cerasela Zoica Issaragrisil, Surapol Chen, Yi Charlie Rojanasakul, Yon |
author_sort | Luanpitpong, Sudjit |
collection | PubMed |
description | Tumor microenvironment has been recognized as a key determinant of tumor formation and metastasis, but how tumor microenvironment is affected by nanomaterials is essentially unknown. Here, we investigated whether carbon nanotubes (CNTs), a widely used nanomaterial with known carcinogenic potential, can affect cancer-associated fibroblasts (CAFs), which are a key component of tumor microenvironment that provides necessary support for tumor growth. We show for the first time that single-walled CNT and to a lesser extent multi-walled and its COOH-functionalized form induced CAF-like cells, which are non-tumorigenic in animals, but promote tumor growth of human lung carcinoma and CNT-transformed lung epithelial cells. The mechanism by which CNT-induced CAF-like cells promote tumor growth involved the acquisition of cancer stem cells (CSCs) in cancer population. Gene knockdown experiments showed that an expression of podoplanin on CAF-like cells is essential for their effects, indicating the functional role of CAF-like cells and podoplanin in CNT tumorigenic process. Our findings unveil a novel mechanism of CNT-induced carcinogenesis through the induction of CAF-like cells that support CSCs and drive tumor formation. Our results also suggest the potential utility of podoplanin as a mechanism-based biomarker for rapid screening of carcinogenicity of CNTs and related nanomaterials for their safer design. |
format | Online Article Text |
id | pubmed-5172236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51722362016-12-28 Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity Luanpitpong, Sudjit Wang, Liying Castranova, Vincent Dinu, Cerasela Zoica Issaragrisil, Surapol Chen, Yi Charlie Rojanasakul, Yon Sci Rep Article Tumor microenvironment has been recognized as a key determinant of tumor formation and metastasis, but how tumor microenvironment is affected by nanomaterials is essentially unknown. Here, we investigated whether carbon nanotubes (CNTs), a widely used nanomaterial with known carcinogenic potential, can affect cancer-associated fibroblasts (CAFs), which are a key component of tumor microenvironment that provides necessary support for tumor growth. We show for the first time that single-walled CNT and to a lesser extent multi-walled and its COOH-functionalized form induced CAF-like cells, which are non-tumorigenic in animals, but promote tumor growth of human lung carcinoma and CNT-transformed lung epithelial cells. The mechanism by which CNT-induced CAF-like cells promote tumor growth involved the acquisition of cancer stem cells (CSCs) in cancer population. Gene knockdown experiments showed that an expression of podoplanin on CAF-like cells is essential for their effects, indicating the functional role of CAF-like cells and podoplanin in CNT tumorigenic process. Our findings unveil a novel mechanism of CNT-induced carcinogenesis through the induction of CAF-like cells that support CSCs and drive tumor formation. Our results also suggest the potential utility of podoplanin as a mechanism-based biomarker for rapid screening of carcinogenicity of CNTs and related nanomaterials for their safer design. Nature Publishing Group 2016-12-20 /pmc/articles/PMC5172236/ /pubmed/27996035 http://dx.doi.org/10.1038/srep39558 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Luanpitpong, Sudjit Wang, Liying Castranova, Vincent Dinu, Cerasela Zoica Issaragrisil, Surapol Chen, Yi Charlie Rojanasakul, Yon Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title | Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title_full | Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title_fullStr | Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title_full_unstemmed | Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title_short | Induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
title_sort | induction of cancer-associated fibroblast-like cells by carbon nanotubes dictates its tumorigenicity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172236/ https://www.ncbi.nlm.nih.gov/pubmed/27996035 http://dx.doi.org/10.1038/srep39558 |
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