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Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells

In recent years, ferroptosis has been investigated widely as a new form of cell death. Development of nanodrugs for ferroptosis induction in cancer cells may be a promising approach for cancer treatment. Here, we developed a type of nanoparticle consisting of the antitumor drug doxorubicin and exoge...

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Detalles Bibliográficos
Autores principales: Yang, Runlin, Li, Yaoqi, Wang, Xinyu, Yan, Junjie, Pan, Donghui, Xu, Yuping, Wang, Lizhen, Yang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071105/
https://www.ncbi.nlm.nih.gov/pubmed/35529630
http://dx.doi.org/10.1039/c9ra04478g
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author Yang, Runlin
Li, Yaoqi
Wang, Xinyu
Yan, Junjie
Pan, Donghui
Xu, Yuping
Wang, Lizhen
Yang, Min
author_facet Yang, Runlin
Li, Yaoqi
Wang, Xinyu
Yan, Junjie
Pan, Donghui
Xu, Yuping
Wang, Lizhen
Yang, Min
author_sort Yang, Runlin
collection PubMed
description In recent years, ferroptosis has been investigated widely as a new form of cell death. Development of nanodrugs for ferroptosis induction in cancer cells may be a promising approach for cancer treatment. Here, we developed a type of nanoparticle consisting of the antitumor drug doxorubicin and exogenous ferritin. The drug loading process did not change the size of ferritin obviously. And this nanoparticle could induce the accumulation of ROS and cell ferroptosis for transferrin receptor overexpressed tumor cell, HT29. The ferroptosis process was also confirmed using inhibitors for ferroptosis. The cytotoxicity of this nanoparticle is similar to that of free DOX. This study provides a new strategy for targeting and killing transferrin receptor overexpressed tumor cells.
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spelling pubmed-90711052022-05-06 Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells Yang, Runlin Li, Yaoqi Wang, Xinyu Yan, Junjie Pan, Donghui Xu, Yuping Wang, Lizhen Yang, Min RSC Adv Chemistry In recent years, ferroptosis has been investigated widely as a new form of cell death. Development of nanodrugs for ferroptosis induction in cancer cells may be a promising approach for cancer treatment. Here, we developed a type of nanoparticle consisting of the antitumor drug doxorubicin and exogenous ferritin. The drug loading process did not change the size of ferritin obviously. And this nanoparticle could induce the accumulation of ROS and cell ferroptosis for transferrin receptor overexpressed tumor cell, HT29. The ferroptosis process was also confirmed using inhibitors for ferroptosis. The cytotoxicity of this nanoparticle is similar to that of free DOX. This study provides a new strategy for targeting and killing transferrin receptor overexpressed tumor cells. The Royal Society of Chemistry 2019-09-10 /pmc/articles/PMC9071105/ /pubmed/35529630 http://dx.doi.org/10.1039/c9ra04478g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Yang, Runlin
Li, Yaoqi
Wang, Xinyu
Yan, Junjie
Pan, Donghui
Xu, Yuping
Wang, Lizhen
Yang, Min
Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title_full Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title_fullStr Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title_full_unstemmed Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title_short Doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
title_sort doxorubicin loaded ferritin nanoparticles for ferroptosis enhanced targeted killing of cancer cells
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071105/
https://www.ncbi.nlm.nih.gov/pubmed/35529630
http://dx.doi.org/10.1039/c9ra04478g
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