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Redox homeostasis disruptors enhanced cuproptosis effect for synergistic photothermal/chemodynamic therapy.
- Source :
-
Journal of colloid and interface science [J Colloid Interface Sci] 2025 Jan 15; Vol. 678 (Pt A), pp. 1060-1074. Date of Electronic Publication: 2024 Aug 31. - Publication Year :
- 2025
-
Abstract
- The combination of chemodynamic therapy (CDT) with photothermal therapy (PTT) is a promising approach to enhance antitumor efficacy of chemotherapeutics. In this paper, we developed novel copper-chelated polydopamine (PDA) nanoparticles (NPs) functionalized with hyaluronic acid (HA) (Cu-PDA-HA NPs) to induce apoptosis and cuproptosis-induced cell death, synergistically combining PTT and CDT. Experimental results revealed that Cu-PDA-HA NPs can respond to excessive glutathione (GSH) and hydrogen peroxide (H <subscript>2</subscript> O <subscript>2</subscript> ) in the tumor microenvironment (TME), which will enable their specific degradation, thereby leading to efficient accumulation of Cu <superscript>2+</superscript> within tumor cells. The released Cu <superscript>2+</superscript> ions were reduced by GSH to generate Cu <superscript>+</superscript> , which catalyzed in situ Fenton-like reactions to produce cytotoxic hydroxyl radicals (·OH), disrupting cellular redox homeostasis and promoting apoptosis-related CDT. Meanwhile, the photothermal effect of the Cu-PDA-HA NPs could enhance oxidative stress within the tumor by elevating the temperature and subsequent ·OH production. The enhanced oxidative stress made tumor cells more vulnerable to cuproptosis-induced toxicity. Furthermore, in vivo experiments demonstrated that Cu-PDA-HA NPs can still undergo a temperature increase of 18.9°C following 808 nm near-infrared irradiation (1.0 W/cm <superscript>2</superscript> , 5 min). Meanwhile, Cu-PDA-HA NPs were able to induce oligomerization of dihydrolipoamide S-acetyltransferase (DLAT) and down-regulate Fe-S cluster proteins such as ferredoxin (FDX1), thereby activating cuproptosis. Therefore, this study provides a novel approach for designing multifunctional nanoparticles with on-demand Cu <superscript>2+</superscript> release and offers a fresh perspective for exploring synergistic therapeutic strategies involving CDT/PTT/apoptosis/cuproptosis.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Humans
Mice
Polymers chemistry
Polymers pharmacology
Hyaluronic Acid chemistry
Hyaluronic Acid pharmacology
Antineoplastic Agents pharmacology
Antineoplastic Agents chemistry
Cell Line, Tumor
Cell Survival drug effects
Particle Size
Surface Properties
Drug Screening Assays, Antitumor
Cell Proliferation drug effects
Copper chemistry
Copper pharmacology
Indoles chemistry
Indoles pharmacology
Homeostasis drug effects
Oxidation-Reduction
Nanoparticles chemistry
Photothermal Therapy
Apoptosis drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1095-7103
- Volume :
- 678
- Issue :
- Pt A
- Database :
- MEDLINE
- Journal :
- Journal of colloid and interface science
- Publication Type :
- Academic Journal
- Accession number :
- 39236435
- Full Text :
- https://doi.org/10.1016/j.jcis.2024.08.234