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Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug
Ferroptosis has emerged as a potent form of no-apoptotic cell death that offers a promising alternative to avoid the chemoresistance of apoptotic pathways and serves as a vulnerability of cancer. Herein, we have constructed a biomimetic self-assembly nano-prodrug system that enables the co-delivery...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616161/ https://www.ncbi.nlm.nih.gov/pubmed/37915761 http://dx.doi.org/10.1016/j.ajps.2023.100844 |
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author | Huang, Yong Lin, Yi Li, Bowen Zhang, Fu Zhan, Chenyue Xie, Xin Yao, Zhuo Wu, Chongzhi Ping, Yuan Shen, Jianliang |
author_facet | Huang, Yong Lin, Yi Li, Bowen Zhang, Fu Zhan, Chenyue Xie, Xin Yao, Zhuo Wu, Chongzhi Ping, Yuan Shen, Jianliang |
author_sort | Huang, Yong |
collection | PubMed |
description | Ferroptosis has emerged as a potent form of no-apoptotic cell death that offers a promising alternative to avoid the chemoresistance of apoptotic pathways and serves as a vulnerability of cancer. Herein, we have constructed a biomimetic self-assembly nano-prodrug system that enables the co-delivery of gefitinib (Gefi), ferrocene (Fc) and dihydroartemisinin (DHA) for the combined therapy of both ferroptosis and apoptosis. In the tumor microenvironment, this nano-prodrug is able to disassemble and trigger drug release under high levels of GSH. Interestingly, the released DHA can downregulate GPX4 level for the enhancement of intracellular ferroptosis from Fc, further executing tumor cell death with concomitant chemotherapy by Gefi. More importantly, this nano-prodrug provides highly homologous targeting ability by coating related cell membranes and exhibits outstanding inhibition of tumor growth and metastasis, as well as no noticeable side-effects during treatments. This simple small molecular self-assembled nano-prodrug provides a new reasonably designed modality for ferroptosis-combined chemotherapy. |
format | Online Article Text |
id | pubmed-10616161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-106161612023-11-01 Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug Huang, Yong Lin, Yi Li, Bowen Zhang, Fu Zhan, Chenyue Xie, Xin Yao, Zhuo Wu, Chongzhi Ping, Yuan Shen, Jianliang Asian J Pharm Sci Original Research Paper Ferroptosis has emerged as a potent form of no-apoptotic cell death that offers a promising alternative to avoid the chemoresistance of apoptotic pathways and serves as a vulnerability of cancer. Herein, we have constructed a biomimetic self-assembly nano-prodrug system that enables the co-delivery of gefitinib (Gefi), ferrocene (Fc) and dihydroartemisinin (DHA) for the combined therapy of both ferroptosis and apoptosis. In the tumor microenvironment, this nano-prodrug is able to disassemble and trigger drug release under high levels of GSH. Interestingly, the released DHA can downregulate GPX4 level for the enhancement of intracellular ferroptosis from Fc, further executing tumor cell death with concomitant chemotherapy by Gefi. More importantly, this nano-prodrug provides highly homologous targeting ability by coating related cell membranes and exhibits outstanding inhibition of tumor growth and metastasis, as well as no noticeable side-effects during treatments. This simple small molecular self-assembled nano-prodrug provides a new reasonably designed modality for ferroptosis-combined chemotherapy. Shenyang Pharmaceutical University 2023-09 2023-08-26 /pmc/articles/PMC10616161/ /pubmed/37915761 http://dx.doi.org/10.1016/j.ajps.2023.100844 Text en © 2023 Shenyang Pharmaceutical University. Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Paper Huang, Yong Lin, Yi Li, Bowen Zhang, Fu Zhan, Chenyue Xie, Xin Yao, Zhuo Wu, Chongzhi Ping, Yuan Shen, Jianliang Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title | Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title_full | Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title_fullStr | Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title_full_unstemmed | Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title_short | Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
title_sort | combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616161/ https://www.ncbi.nlm.nih.gov/pubmed/37915761 http://dx.doi.org/10.1016/j.ajps.2023.100844 |
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