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Nanoparticles for Ferroptosis Therapy in Cancer.

作者信息

Zaffaroni Nadia, Beretta Giovanni Luca

机构信息

Molecular Pharmacology Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.

出版信息

Pharmaceutics. 2021 Oct 25;13(11):1785. doi: 10.3390/pharmaceutics13111785.


DOI:10.3390/pharmaceutics13111785
PMID:34834199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8620841/
Abstract

Ferroptosis is a regulated cell death mechanism holding promise for anticancer therapy. Numerous small molecules inducing ferroptosis have been reported thus far. However, these compounds suffer from important drawbacks including poor solubility, systemic toxicity, and scarce tumor targeting ability that have limited their clinical success. The notion that nanoparticles inducing ferroptosis show better preclinical profiles compared to small molecules and overcome resistance to apoptosis has opened a new scenario for cancer treatment. Due to peculiar chemical-physical properties, nanoparticles can be loaded with anticancer drugs or decorated with tumor-selecting molecules. These features allow for drug combination treatment as well as tumor targeting. In the review, we summarize and discuss the available information concerning nanoparticles inducing ferroptosis endowed with different peculiarities and suitable for therapeutic purposes including nanoparticles for (i) antitumor drug delivery, (ii) tumor targeting, (iii) immunomodulation, and (iv) radiofrequency ablation, hyperthermia, and photodynamic therapy.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/30c1d960afc1/pharmaceutics-13-01785-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/737c428b2f04/pharmaceutics-13-01785-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/1a30e2c3e450/pharmaceutics-13-01785-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/30c1d960afc1/pharmaceutics-13-01785-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/737c428b2f04/pharmaceutics-13-01785-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/1a30e2c3e450/pharmaceutics-13-01785-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd4/8620841/30c1d960afc1/pharmaceutics-13-01785-g003.jpg

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[1]
Nanoparticles for Ferroptosis Therapy in Cancer.

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

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[2]
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[3]
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Int J Biol Sci. 2025-6-9

[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Ferroptosis-Strengthened Metabolic and Inflammatory Regulation of Tumor-Associated Macrophages Provokes Potent Tumoricidal Activities.

Nano Lett. 2021-8-11

[2]
Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses.

Nat Commun. 2021-7-14

[3]
Effect of Malt-PEG-Abz@RSL3 micelles on HepG2 cells based on NADPH depletion and GPX4 inhibition in ferroptosis.

J Drug Target. 2022-2

[4]
A Ferrocene-Functionalized Covalent Organic Framework for Enhancing Chemodynamic Therapy via Redox Dyshomeostasis.

Small. 2021-8

[5]
An innovative NRF2 nano-modulator induces lung cancer ferroptosis and elicits an immunostimulatory tumor microenvironment.

Theranostics. 2021

[6]
The potential application of nanomaterials for ferroptosis-based cancer therapy.

Biomed Mater. 2021-6-11

[7]
Multifunctional biomolecule nanostructures for cancer therapy.

Nat Rev Mater. 2021

[8]
Metabolic Control by Heat Stress Determining Cell Fate to Ferroptosis for Effective Cancer Therapy.

ACS Nano. 2021-4-27

[9]
High-Performance Self-Cascade Pyrite Nanozymes for Apoptosis-Ferroptosis Synergistic Tumor Therapy.

ACS Nano. 2021-3-23

[10]
Blue light-triggered Fe-release from monodispersed ferrihydrite nanoparticles for cancer iron therapy.

Biomaterials. 2021-4

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