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Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy

Selective delivery of photosensitizers to mitochondria of cancer cells can enhance the efficacy of photodynamic therapy (PDT). Though cationic Ru-based photosensitizers accumulate in mitochondria, they require excitation with less penetrating short-wavelength photons, limiting their application in P...

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Autores principales: Ni, Kaiyuan, Lan, Guangxu, Veroneau, Samuel S., Duan, Xiaopin, Song, Yang, Lin, Wenbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193046/
https://www.ncbi.nlm.nih.gov/pubmed/30333489
http://dx.doi.org/10.1038/s41467-018-06655-7
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author Ni, Kaiyuan
Lan, Guangxu
Veroneau, Samuel S.
Duan, Xiaopin
Song, Yang
Lin, Wenbin
author_facet Ni, Kaiyuan
Lan, Guangxu
Veroneau, Samuel S.
Duan, Xiaopin
Song, Yang
Lin, Wenbin
author_sort Ni, Kaiyuan
collection PubMed
description Selective delivery of photosensitizers to mitochondria of cancer cells can enhance the efficacy of photodynamic therapy (PDT). Though cationic Ru-based photosensitizers accumulate in mitochondria, they require excitation with less penetrating short-wavelength photons, limiting their application in PDT. We recently discovered X-ray based cancer therapy by nanoscale metal–organic frameworks (nMOFs) via enhancing radiotherapy (RT) and enabling radiodynamic therapy (RDT). Herein we report Hf-DBB-Ru as a mitochondria-targeted nMOF for RT-RDT. Constructed from Ru-based photosensitizers, the cationic framework exhibits strong mitochondria-targeting property. Upon X-ray irradiation, Hf-DBB-Ru efficiently generates hydroxyl radicals from the Hf(6) SBUs and singlet oxygen from the DBB-Ru photosensitizers to lead to RT-RDT effects. Mitochondria-targeted RT-RDT depolarizes the mitochondrial membrane to initiate apoptosis of cancer cells, leading to significant regression of colorectal tumors in mouse models. Our work establishes an effective strategy to selectively target mitochondria with cationic nMOFs for enhanced cancer therapy via RT-RDT with low doses of deeply penetrating X-rays.
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spelling pubmed-61930462018-10-19 Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy Ni, Kaiyuan Lan, Guangxu Veroneau, Samuel S. Duan, Xiaopin Song, Yang Lin, Wenbin Nat Commun Article Selective delivery of photosensitizers to mitochondria of cancer cells can enhance the efficacy of photodynamic therapy (PDT). Though cationic Ru-based photosensitizers accumulate in mitochondria, they require excitation with less penetrating short-wavelength photons, limiting their application in PDT. We recently discovered X-ray based cancer therapy by nanoscale metal–organic frameworks (nMOFs) via enhancing radiotherapy (RT) and enabling radiodynamic therapy (RDT). Herein we report Hf-DBB-Ru as a mitochondria-targeted nMOF for RT-RDT. Constructed from Ru-based photosensitizers, the cationic framework exhibits strong mitochondria-targeting property. Upon X-ray irradiation, Hf-DBB-Ru efficiently generates hydroxyl radicals from the Hf(6) SBUs and singlet oxygen from the DBB-Ru photosensitizers to lead to RT-RDT effects. Mitochondria-targeted RT-RDT depolarizes the mitochondrial membrane to initiate apoptosis of cancer cells, leading to significant regression of colorectal tumors in mouse models. Our work establishes an effective strategy to selectively target mitochondria with cationic nMOFs for enhanced cancer therapy via RT-RDT with low doses of deeply penetrating X-rays. Nature Publishing Group UK 2018-10-17 /pmc/articles/PMC6193046/ /pubmed/30333489 http://dx.doi.org/10.1038/s41467-018-06655-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ni, Kaiyuan
Lan, Guangxu
Veroneau, Samuel S.
Duan, Xiaopin
Song, Yang
Lin, Wenbin
Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title_full Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title_fullStr Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title_full_unstemmed Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title_short Nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
title_sort nanoscale metal-organic frameworks for mitochondria-targeted radiotherapy-radiodynamic therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193046/
https://www.ncbi.nlm.nih.gov/pubmed/30333489
http://dx.doi.org/10.1038/s41467-018-06655-7
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