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Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation

The escape of bladder cancer from immunosurveillance causes monotherapy to exhibit poor efficacy; therefore, designing a multifunctional nanoparticle that boosts programmed cell death and immunoactivation has potential as a treatment strategy. Herein, we developed a facile one-pot coprecipitation re...

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Autores principales: Chin, Yu-Cheng, Yang, Li-Xing, Hsu, Fei-Ting, Hsu, Che-Wei, Chang, Te-Wei, Chen, Hsi-Ying, Chen, Linda Yen-Chien, Chia, Zi Chun, Hung, Chun-Hua, Su, Wu-Chou, Chiu, Yi-Chun, Huang, Chih-Chia, Liao, Mei-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367122/
https://www.ncbi.nlm.nih.gov/pubmed/35953837
http://dx.doi.org/10.1186/s12951-022-01575-7
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author Chin, Yu-Cheng
Yang, Li-Xing
Hsu, Fei-Ting
Hsu, Che-Wei
Chang, Te-Wei
Chen, Hsi-Ying
Chen, Linda Yen-Chien
Chia, Zi Chun
Hung, Chun-Hua
Su, Wu-Chou
Chiu, Yi-Chun
Huang, Chih-Chia
Liao, Mei-Yi
author_facet Chin, Yu-Cheng
Yang, Li-Xing
Hsu, Fei-Ting
Hsu, Che-Wei
Chang, Te-Wei
Chen, Hsi-Ying
Chen, Linda Yen-Chien
Chia, Zi Chun
Hung, Chun-Hua
Su, Wu-Chou
Chiu, Yi-Chun
Huang, Chih-Chia
Liao, Mei-Yi
author_sort Chin, Yu-Cheng
collection PubMed
description The escape of bladder cancer from immunosurveillance causes monotherapy to exhibit poor efficacy; therefore, designing a multifunctional nanoparticle that boosts programmed cell death and immunoactivation has potential as a treatment strategy. Herein, we developed a facile one-pot coprecipitation reaction to fabricate cluster-structured nanoparticles (CNPs) assembled from Fe(3)O(4) and iron chlorophyll (Chl/Fe) photosensitizers. This nanoassembled CNP, as a multifunctional theranostic agent, could perform red-NIR fluorescence and change the redox balance by the photoinduction of reactive oxygen species (ROS) and attenuate iron-mediated lipid peroxidation by the induction of a Fenton-like reaction. The intravesical instillation of Fe(3)O(4)@Chl/Fe CNPs modified with 4-carboxyphenylboronic acid (CPBA) may target the BC wall through glycoproteins in the BC cavity, allowing local killing of cancer cells by photodynamic therapy (PDT)-induced singlet oxygen and causing chemodynamic therapy (CDT)-mediated ferroptosis. An interesting possibility is reprogramming of the tumor microenvironment from immunosuppressive to immunostimulatory after PDT-CDT treatment, which was demonstrated by the reduction of PD-L1 (lower “off” signal to the effector immune cells), IDO-1, TGF-β, and M2-like macrophages and the induction of CD8(+) T cells on BC sections. Moreover, the intravesical instillation of Fe(3)O(4)@Chl/Fe CNPs may enhance the large-area distribution on the BC wall, improving antitumor efficacy and increasing survival rates from 0 to 91.7%. Our theranostic CNPs not only demonstrated combined PDT-CDT-induced cytotoxicity, ROS production, and ferroptosis to facilitate treatment efficacy but also opened up new horizons for eliminating the immunosuppressive effect by simultaneous PDT-CDT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01575-7.
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spelling pubmed-93671222022-08-12 Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation Chin, Yu-Cheng Yang, Li-Xing Hsu, Fei-Ting Hsu, Che-Wei Chang, Te-Wei Chen, Hsi-Ying Chen, Linda Yen-Chien Chia, Zi Chun Hung, Chun-Hua Su, Wu-Chou Chiu, Yi-Chun Huang, Chih-Chia Liao, Mei-Yi J Nanobiotechnology Research The escape of bladder cancer from immunosurveillance causes monotherapy to exhibit poor efficacy; therefore, designing a multifunctional nanoparticle that boosts programmed cell death and immunoactivation has potential as a treatment strategy. Herein, we developed a facile one-pot coprecipitation reaction to fabricate cluster-structured nanoparticles (CNPs) assembled from Fe(3)O(4) and iron chlorophyll (Chl/Fe) photosensitizers. This nanoassembled CNP, as a multifunctional theranostic agent, could perform red-NIR fluorescence and change the redox balance by the photoinduction of reactive oxygen species (ROS) and attenuate iron-mediated lipid peroxidation by the induction of a Fenton-like reaction. The intravesical instillation of Fe(3)O(4)@Chl/Fe CNPs modified with 4-carboxyphenylboronic acid (CPBA) may target the BC wall through glycoproteins in the BC cavity, allowing local killing of cancer cells by photodynamic therapy (PDT)-induced singlet oxygen and causing chemodynamic therapy (CDT)-mediated ferroptosis. An interesting possibility is reprogramming of the tumor microenvironment from immunosuppressive to immunostimulatory after PDT-CDT treatment, which was demonstrated by the reduction of PD-L1 (lower “off” signal to the effector immune cells), IDO-1, TGF-β, and M2-like macrophages and the induction of CD8(+) T cells on BC sections. Moreover, the intravesical instillation of Fe(3)O(4)@Chl/Fe CNPs may enhance the large-area distribution on the BC wall, improving antitumor efficacy and increasing survival rates from 0 to 91.7%. Our theranostic CNPs not only demonstrated combined PDT-CDT-induced cytotoxicity, ROS production, and ferroptosis to facilitate treatment efficacy but also opened up new horizons for eliminating the immunosuppressive effect by simultaneous PDT-CDT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01575-7. BioMed Central 2022-08-11 /pmc/articles/PMC9367122/ /pubmed/35953837 http://dx.doi.org/10.1186/s12951-022-01575-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Chin, Yu-Cheng
Yang, Li-Xing
Hsu, Fei-Ting
Hsu, Che-Wei
Chang, Te-Wei
Chen, Hsi-Ying
Chen, Linda Yen-Chien
Chia, Zi Chun
Hung, Chun-Hua
Su, Wu-Chou
Chiu, Yi-Chun
Huang, Chih-Chia
Liao, Mei-Yi
Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title_full Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title_fullStr Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title_full_unstemmed Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title_short Iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
title_sort iron oxide@chlorophyll clustered nanoparticles eliminate bladder cancer by photodynamic immunotherapy-initiated ferroptosis and immunostimulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367122/
https://www.ncbi.nlm.nih.gov/pubmed/35953837
http://dx.doi.org/10.1186/s12951-022-01575-7
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