2022
DOI: 10.1016/j.jconrel.2021.12.016
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Copper arsenite-complexed Fenton-like nanoparticles as oxidative stress-amplifying anticancer agents

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Cited by 16 publications
(8 citation statements)
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“…Moreover, Lee et al. 441 reported using copper (II) arsenite (CuAS) coupled in the core domains of poly (ethylene glycol)‐ b ‐poly(3,4‐dihydroxy‐ L ‐phenylalanine) to form CuAS‐PMs for CDT treatment of cancer.…”
Section: Application Strategies Of Multifunctional Nanoparticlesmentioning
confidence: 99%
See 1 more Smart Citation
“…Moreover, Lee et al. 441 reported using copper (II) arsenite (CuAS) coupled in the core domains of poly (ethylene glycol)‐ b ‐poly(3,4‐dihydroxy‐ L ‐phenylalanine) to form CuAS‐PMs for CDT treatment of cancer.…”
Section: Application Strategies Of Multifunctional Nanoparticlesmentioning
confidence: 99%
“…In their results, the tumor growth in U87MG tumor‐bearing mice was significantly inhibited and showed higher rates of apoptosis than control groups after intravenous injection of MS@MnO 2 nanoparticles. Moreover, Lee et al 441 . reported using copper (II) arsenite (CuAS) coupled in the core domains of poly (ethylene glycol)‐ b ‐poly(3,4‐dihydroxy‐ L ‐phenylalanine) to form CuAS‐PMs for CDT treatment of cancer.…”
Section: Application Strategies Of Multifunctional Nanoparticlesmentioning
confidence: 99%
“…However, with the deepening of research, researchers have shown that Cu buildup can potentially result in cell death or irreversible harm to cells, such as cuproptosis, 45–47 apoptosis, 48,49 pyroptosis, 50,51 and ferroptosis 52,53 . In addition, the transformation of Cu 2+ and Cu + sensitizes Fenton‐like reaction and consumes glutathione (GSH), promoting intracellular oxidative stress 54–63 . All of these suggest that Cu ion interference therapy containing Cu exhaustion as well as Cu supplementation has become an attractive therapeutic strategy in anticancer therapy 64–66 .…”
Section: Introductionmentioning
confidence: 99%
“…52,53 In addition, the transformation of Cu 2+ and Cu + sensitizes Fenton-like reaction and consumes glutathione (GSH), promoting intracellular oxidative stress. [54][55][56][57][58][59][60][61][62][63] All of these suggest that Cu ion interference therapy containing Cu exhaustion as well as Cu supplementation has become an attractive therapeutic strategy in anticancer therapy. [64][65][66] It is true that life is Cu and death is Cu.…”
mentioning
confidence: 99%
“…17,18 Although some substantial efforts have revealed that the H 2 O 2 abundance in cancer cells is higher than that in normal cells, its abundance is insufficient to generate adequate ˙OH by Fenton-like reactions for amplifying oxidative stress in the TME. 19,20 Recently, to settle this point of inadequate H 2 O 2 , a large number of studies have been directed toward the delivery of exogenous H 2 O 2 , 21 amplification of endogenous H 2 O 2 , 22 or decomposition of metal peroxides. 23 For example, natural glucose oxidase as a kind of H 2 O 2 producer can greatly amplify H 2 O 2 abundance in the TME.…”
Section: Introductionmentioning
confidence: 99%