Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance
Multidrug resistance is a major challenge in cancer therapy. Here, the authors develop a mitochondria-targeting nanoparticle system that inhibits adenosine triphosphate transporter activity via reactive oxygen species generation and can thus be used to target multidrug-resistant cancer.
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2018-02-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-02915-8 |
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doaj-1411ae0882f24d7aa8a64b2cb0d42b7e2021-05-11T09:59:53ZengNature Publishing GroupNature Communications2041-17232018-02-019111610.1038/s41467-018-02915-8Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistanceHai Wang0Zan Gao1Xuanyou Liu2Pranay Agarwal3Shuting Zhao4Daniel W. Conroy5Guang Ji6Jianhua Yu7Christopher P. Jaroniec8Zhenguo Liu9Xiongbin Lu10Xiaodong Li11Xiaoming He12Department of Biomedical Engineering, The Ohio State UniversityDepartment of Mechanical and Aerospace Engineering, University of VirginiaDivision of Cardiovascular Medicine, Center for Precision Medicine, University of Missouri School of MedicineDepartment of Biomedical Engineering, The Ohio State UniversityDepartment of Biomedical Engineering, The Ohio State UniversityDepartment of Chemistry and Biochemistry, The Ohio State UniversityInstitute of Digestive Diseases, Longhua Hospital, Shanghai University of Traditional Chinese MedicineComprehensive Cancer Center, The Ohio State UniversityDepartment of Chemistry and Biochemistry, The Ohio State UniversityDavis Heart and Lung Research Institute, The Ohio State UniversityDepartment of Medical and Molecular Genetics and Melvin and Bren Simon Cancer Center, Indiana University School of MedicineDepartment of Mechanical and Aerospace Engineering, University of VirginiaDepartment of Biomedical Engineering, The Ohio State UniversityMultidrug resistance is a major challenge in cancer therapy. Here, the authors develop a mitochondria-targeting nanoparticle system that inhibits adenosine triphosphate transporter activity via reactive oxygen species generation and can thus be used to target multidrug-resistant cancer.https://doi.org/10.1038/s41467-018-02915-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hai Wang Zan Gao Xuanyou Liu Pranay Agarwal Shuting Zhao Daniel W. Conroy Guang Ji Jianhua Yu Christopher P. Jaroniec Zhenguo Liu Xiongbin Lu Xiaodong Li Xiaoming He |
spellingShingle |
Hai Wang Zan Gao Xuanyou Liu Pranay Agarwal Shuting Zhao Daniel W. Conroy Guang Ji Jianhua Yu Christopher P. Jaroniec Zhenguo Liu Xiongbin Lu Xiaodong Li Xiaoming He Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance Nature Communications |
author_facet |
Hai Wang Zan Gao Xuanyou Liu Pranay Agarwal Shuting Zhao Daniel W. Conroy Guang Ji Jianhua Yu Christopher P. Jaroniec Zhenguo Liu Xiongbin Lu Xiaodong Li Xiaoming He |
author_sort |
Hai Wang |
title |
Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
title_short |
Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
title_full |
Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
title_fullStr |
Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
title_full_unstemmed |
Targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
title_sort |
targeted production of reactive oxygen species in mitochondria to overcome cancer drug resistance |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2018-02-01 |
description |
Multidrug resistance is a major challenge in cancer therapy. Here, the authors develop a mitochondria-targeting nanoparticle system that inhibits adenosine triphosphate transporter activity via reactive oxygen species generation and can thus be used to target multidrug-resistant cancer. |
url |
https://doi.org/10.1038/s41467-018-02915-8 |
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