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Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy

Immunogenic cell death (ICD) through apoptosis or necroptosis is widely adopted to improve the therapeutic effect in cancer treatment by triggering a specific antitumor immunity. However, the tumor resistance to apoptosis/necroptosis seriously impedes the therapeutic effect. Recently, ferroptosis fe...

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Autores principales: Chen, Chao, Wang, Zaiyu, Jia, Shaorui, Zhang, Yuan, Ji, Shenglu, Zhao, Zheng, Kwok, Ryan T. K., Lam, Jacky W. Y., Ding, Dan, Shi, Yang, Tang, Ben Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981454/
https://www.ncbi.nlm.nih.gov/pubmed/35132824
http://dx.doi.org/10.1002/advs.202104885
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author Chen, Chao
Wang, Zaiyu
Jia, Shaorui
Zhang, Yuan
Ji, Shenglu
Zhao, Zheng
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Ding, Dan
Shi, Yang
Tang, Ben Zhong
author_facet Chen, Chao
Wang, Zaiyu
Jia, Shaorui
Zhang, Yuan
Ji, Shenglu
Zhao, Zheng
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Ding, Dan
Shi, Yang
Tang, Ben Zhong
author_sort Chen, Chao
collection PubMed
description Immunogenic cell death (ICD) through apoptosis or necroptosis is widely adopted to improve the therapeutic effect in cancer treatment by triggering a specific antitumor immunity. However, the tumor resistance to apoptosis/necroptosis seriously impedes the therapeutic effect. Recently, ferroptosis featured with excessive lipid peroxidation is demonstrated capable of bypassing the apoptosis/necroptosis resistance to kill cancer cells. To date, numerous efficient ferroptosis inducers are developed and successfully utilized for sensitizing cancer cells to ferroptosis. Unfortunately, these inducers can hardly generate adequate immunogenicity during induction of ferroptotic cancer cell death, which distinctly attenuates the efficacy of triggering antitumor immune response, therefore leads to unsatisfactory therapeutic effect. Herein, a novel high‐performance photothermal nanoparticle (TPA‐NDTA NP) is designed by exploiting energy via excited‐state intramolecular motion and employed for immensely assisting ferroptosis inducer to evoke highly efficient ICD through ferroptosis pathway. Tumor models with poor immunogenicity are used to demonstrate the tremendously enhanced therapeutic effect endowed by highly enhanced immunogenic ferroptosis in vitro and in vivo by virtue of the NPs. This study sheds new light on a previously unrecognized facet of boosting the immunogenicity of ferroptosis for achieving satisfactory therapeutic effect in cancer therapy.
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spelling pubmed-89814542022-04-11 Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy Chen, Chao Wang, Zaiyu Jia, Shaorui Zhang, Yuan Ji, Shenglu Zhao, Zheng Kwok, Ryan T. K. Lam, Jacky W. Y. Ding, Dan Shi, Yang Tang, Ben Zhong Adv Sci (Weinh) Research Articles Immunogenic cell death (ICD) through apoptosis or necroptosis is widely adopted to improve the therapeutic effect in cancer treatment by triggering a specific antitumor immunity. However, the tumor resistance to apoptosis/necroptosis seriously impedes the therapeutic effect. Recently, ferroptosis featured with excessive lipid peroxidation is demonstrated capable of bypassing the apoptosis/necroptosis resistance to kill cancer cells. To date, numerous efficient ferroptosis inducers are developed and successfully utilized for sensitizing cancer cells to ferroptosis. Unfortunately, these inducers can hardly generate adequate immunogenicity during induction of ferroptotic cancer cell death, which distinctly attenuates the efficacy of triggering antitumor immune response, therefore leads to unsatisfactory therapeutic effect. Herein, a novel high‐performance photothermal nanoparticle (TPA‐NDTA NP) is designed by exploiting energy via excited‐state intramolecular motion and employed for immensely assisting ferroptosis inducer to evoke highly efficient ICD through ferroptosis pathway. Tumor models with poor immunogenicity are used to demonstrate the tremendously enhanced therapeutic effect endowed by highly enhanced immunogenic ferroptosis in vitro and in vivo by virtue of the NPs. This study sheds new light on a previously unrecognized facet of boosting the immunogenicity of ferroptosis for achieving satisfactory therapeutic effect in cancer therapy. John Wiley and Sons Inc. 2022-02-08 /pmc/articles/PMC8981454/ /pubmed/35132824 http://dx.doi.org/10.1002/advs.202104885 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Chen, Chao
Wang, Zaiyu
Jia, Shaorui
Zhang, Yuan
Ji, Shenglu
Zhao, Zheng
Kwok, Ryan T. K.
Lam, Jacky W. Y.
Ding, Dan
Shi, Yang
Tang, Ben Zhong
Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title_full Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title_fullStr Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title_full_unstemmed Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title_short Evoking Highly Immunogenic Ferroptosis Aided by Intramolecular Motion‐Induced Photo‐Hyperthermia for Cancer Therapy
title_sort evoking highly immunogenic ferroptosis aided by intramolecular motion‐induced photo‐hyperthermia for cancer therapy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981454/
https://www.ncbi.nlm.nih.gov/pubmed/35132824
http://dx.doi.org/10.1002/advs.202104885
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