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Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor
The contemporary use of nanomedicines for cancer treatment has been largely limited to serving as carriers for existing therapeutic agents. Here, we provide definitive evidence that, the metallofullerenol nanomaterial Gd@C(82)(OH)(22), while essentially not toxic to normal mammary epithelial cells,...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354030/ https://www.ncbi.nlm.nih.gov/pubmed/25612916 http://dx.doi.org/10.1038/ncomms6988 |
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author | Liu, Ying Chen, Chunying Qian, Pengxu Lu, Xuefei Sun, Baoyun Zhang, Xiao Wang, Liming Gao, Xingfa Li, Han Chen, Zhiyun Tang, Jinglong Zhang, Weijie Dong, Jinquan Bai, Ru Lobie, Peter E. Wu, Qingfa Liu, Suling Zhang, Huafeng Zhao, Feng Wicha, Max S. Zhu, Tao Zhao, Yuliang |
author_facet | Liu, Ying Chen, Chunying Qian, Pengxu Lu, Xuefei Sun, Baoyun Zhang, Xiao Wang, Liming Gao, Xingfa Li, Han Chen, Zhiyun Tang, Jinglong Zhang, Weijie Dong, Jinquan Bai, Ru Lobie, Peter E. Wu, Qingfa Liu, Suling Zhang, Huafeng Zhao, Feng Wicha, Max S. Zhu, Tao Zhao, Yuliang |
author_sort | Liu, Ying |
collection | PubMed |
description | The contemporary use of nanomedicines for cancer treatment has been largely limited to serving as carriers for existing therapeutic agents. Here, we provide definitive evidence that, the metallofullerenol nanomaterial Gd@C(82)(OH)(22), while essentially not toxic to normal mammary epithelial cells, possesses intrinsic inhibitory activity against triple-negative breast cancer cells. Gd@C(82)(OH)(22) blocks epithelial-to-mesenchymal transition with resultant efficient elimination of breast cancer stem cells (CSCs) resulting in abrogation of tumour initiation and metastasis. In normoxic conditions, Gd@C(82)(OH)(22) mediates these effects by blocking TGF-β signalling. Moreover, under hypoxic conditions found in the tumour microenvironment, cellular uptake of Gd@C(82)(OH)(22) is facilitated where it functions as a bi-potent inhibitor of HIF-1α and TGF-β activities, enhancing CSC elimination. These studies indicate that nanomaterials can be engineered to directly target CSCs. Thus, Gd-metallofullerenol is identified as a kind of non-toxic CSC specific inhibitors with significant therapeutic potential. |
format | Online Article Text |
id | pubmed-4354030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43540302015-03-20 Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor Liu, Ying Chen, Chunying Qian, Pengxu Lu, Xuefei Sun, Baoyun Zhang, Xiao Wang, Liming Gao, Xingfa Li, Han Chen, Zhiyun Tang, Jinglong Zhang, Weijie Dong, Jinquan Bai, Ru Lobie, Peter E. Wu, Qingfa Liu, Suling Zhang, Huafeng Zhao, Feng Wicha, Max S. Zhu, Tao Zhao, Yuliang Nat Commun Article The contemporary use of nanomedicines for cancer treatment has been largely limited to serving as carriers for existing therapeutic agents. Here, we provide definitive evidence that, the metallofullerenol nanomaterial Gd@C(82)(OH)(22), while essentially not toxic to normal mammary epithelial cells, possesses intrinsic inhibitory activity against triple-negative breast cancer cells. Gd@C(82)(OH)(22) blocks epithelial-to-mesenchymal transition with resultant efficient elimination of breast cancer stem cells (CSCs) resulting in abrogation of tumour initiation and metastasis. In normoxic conditions, Gd@C(82)(OH)(22) mediates these effects by blocking TGF-β signalling. Moreover, under hypoxic conditions found in the tumour microenvironment, cellular uptake of Gd@C(82)(OH)(22) is facilitated where it functions as a bi-potent inhibitor of HIF-1α and TGF-β activities, enhancing CSC elimination. These studies indicate that nanomaterials can be engineered to directly target CSCs. Thus, Gd-metallofullerenol is identified as a kind of non-toxic CSC specific inhibitors with significant therapeutic potential. Nature Pub. Group 2015-01-23 /pmc/articles/PMC4354030/ /pubmed/25612916 http://dx.doi.org/10.1038/ncomms6988 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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 Liu, Ying Chen, Chunying Qian, Pengxu Lu, Xuefei Sun, Baoyun Zhang, Xiao Wang, Liming Gao, Xingfa Li, Han Chen, Zhiyun Tang, Jinglong Zhang, Weijie Dong, Jinquan Bai, Ru Lobie, Peter E. Wu, Qingfa Liu, Suling Zhang, Huafeng Zhao, Feng Wicha, Max S. Zhu, Tao Zhao, Yuliang Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title | Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title_full | Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title_fullStr | Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title_full_unstemmed | Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title_short | Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
title_sort | gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354030/ https://www.ncbi.nlm.nih.gov/pubmed/25612916 http://dx.doi.org/10.1038/ncomms6988 |
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