CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Journal Year: 2023, Volume and Issue: 47, P. 1 - 31
Published: March 21, 2023
Language: Английский
CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Journal Year: 2023, Volume and Issue: 47, P. 1 - 31
Published: March 21, 2023
Language: Английский
Matter, Journal Year: 2022, Volume and Issue: 5(10), P. 3341 - 3374
Published: Oct. 1, 2022
Language: Английский
Citations
83Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(12)
Published: Jan. 28, 2023
Abstract Lipid peroxidation (LPO) is one of the most damaging processes in chemodynamic therapy (CDT). Although it well known that polyunsaturated fatty acids (PUFAs) are much more susceptible than saturated or monounsaturated ones to LPO, there no study exploring effect cell membrane unsaturation degree on CDT. Here, we report a self‐reinforcing CDT agent (denoted as OA@Fe‐SAC@EM NPs), consisting oleanolic acid (OA)‐loaded iron single‐atom catalyst (Fe‐SAC)‐embedded hollow carbon nanospheres encapsulated by an erythrocyte (EM), which promotes LPO improve efficacy via modulating unsaturation. Upon uptake NPs cancer cells, Fe‐SAC‐catalyzed conversion endogenous hydrogen peroxide into hydroxyl radicals, addition initiating therapeutic process, causes dissociation EM shell and ensuing release OA can enrich cellular membranes with PUFAs, enabling amplification‐enhanced
Language: Английский
Citations
81ACS Nano, Journal Year: 2023, Volume and Issue: 17(3), P. 3064 - 3076
Published: Jan. 16, 2023
As a rising generation of nanozymes, single atom enzymes show significant promise for cancer therapy, due to their maximum utilization efficiency and well-defined electronic structures. However, it remains tremendous challenge precisely produce heteroatom-doped enzyme with an expected coordination environment. Herein, we develop anion exchange strategy controlled production edge-rich sulfur (S)- nitrogen (N)-decorated nickel (S-N/Ni PSAE). In particular, sulfurized S-N/Ni PSAE exhibits stronger peroxidase-like glutathione oxidase-like activities than the nitrogen-monodoped enzyme, which is attributed vacancies defective sites atoms. Moreover, both in vitro vivo results demonstrate that, compared N/Ni PSAE, more effectively triggers ferroptosis tumor cells via inactivating peroxidase 4 inducing lipid peroxidation. This study highlights enhanced catalytic efficacy polynary ferroptosis-based therapy.
Language: Английский
Citations
80TrAC Trends in Analytical Chemistry, Journal Year: 2023, Volume and Issue: 166, P. 117220 - 117220
Published: Aug. 3, 2023
Language: Английский
Citations
79Cell Death and Disease, Journal Year: 2022, Volume and Issue: 13(11)
Published: Nov. 5, 2022
Abstract The term ferroptosis was put forward in 2012 and has been researched exponentially over the past few years. Ferroptosis is an unconventional pattern of iron-dependent programmed cell death, which belongs to a type necrosis distinguished from apoptosis autophagy. Actuated by phospholipid peroxidation, modulated various cellular metabolic signaling pathways, including amino acid, lipid, iron, mitochondrial metabolism. Notably, associated with numerous diseases plays double-edged sword role. Particularly, metastasis-prone or highly-mutated tumor cells are sensitive ferroptosis. Hence, inducing prohibiting vastly promising potential treating drug-resistant cancers. Immunotolerant cancer not traditional death pathway such as necroptosis, while crucial role mediating immune antagonize tolerance, broad prospects clinical setting. Herein, we summarized mechanisms delineated regulatory network ferroptosis, emphasized its dual proposed significant benefits microenvironment, ultimately presented some provocative doubts. This review aims provide practical guidelines research directions for practice immune-resistant tumors.
Language: Английский
Citations
75Advanced Healthcare Materials, Journal Year: 2023, Volume and Issue: 12(13)
Published: Jan. 30, 2023
Cuproptosis is a recently discovered form of programmed cell death and shows great potential in cancer treatment. Herein, copper-dithiocarbamate chelate-doped artemisinin-loaded hollow nanoplatform (HNP) developed via chelation competition-induced hollowing strategy for cuproptosis-based combination therapy. The HNP exhibits tumor microenvironment-triggered catalytic activity, wherein liberated Cu2+ catalyzes artemisinin endogenous H2 O2 to produce C-centered radicals hydroxyl radicals, respectively. Meanwhile, the disulfide bonds-rich can deplete intracellular glutathione, thus triply amplifying oxidative stress. augmented stress sensitizes cells cuproptosis, causing prominent dihydrolipoamide S-acetyltransferase oligomerization mitochondrial dysfunction. Moreover, activate ferroptosis inhibiting GPX4 activity trigger apoptosis dithiocarbamate-copper chelate-mediated ubiquitinated proteins accumulation, resulting potent antitumor efficacy. Such cuproptosis/ferroptosis/apoptosis synergetic opens new avenue
Language: Английский
Citations
63Small, Journal Year: 2023, Volume and Issue: 19(30)
Published: April 14, 2023
Abstract Nanomaterials with enzyme‐mimicking properties, coined as nanozymes, are a promising alternative to natural enzymes owing their remarkable advantages, such high stability, easy preparation, and favorable catalytic performance. Recently, the rapid development of nanotechnology characterization techniques, single atom nanozymes (SAzymes) atomically dispersed active sites, well‐defined electronic geometric structures, tunable coordination environment, maximum metal utilization developed exploited. With superior performance selectivity, SAzymes have made impressive progress in biomedical applications expected bridge gap between artificial enzymes. Herein, recent advances SAzyme preparation methods, mechanisms, systematically summarized. Their cancer therapy, oxidative stress cytoprotection, antibacterial biosensing discussed depth. Furthermore, appreciate these advances, main challenges, prospects for future also outlined highlighted this review.
Language: Английский
Citations
56Advanced Science, Journal Year: 2023, Volume and Issue: 10(13)
Published: Feb. 27, 2023
With the threat posed by drug-resistant pathogenic bacteria, developing non-antibiotic strategies for eradicating clinically prevalent superbugs remains challenging. Ferroptosis is a newly discovered form of regulated cell death that can overcome drug resistance. Emerging evidence shows potential triggering ferroptosis-like antibacterial therapy, but direct delivery iron species inefficient and may cause detrimental effects. Herein, an effective strategy to induce bacterial nonferrous coordinating single-atom metal sites (e.g., Ir Ru) into sp
Language: Английский
Citations
51Advanced Functional Materials, Journal Year: 2023, Volume and Issue: 33(48)
Published: July 21, 2023
Abstract Single‐atom nanozymes (SAzymes) are considered as the most promising candidates for natural enzymes due to their atomically dispersed active sites that closely resemble metal centers of counterparts. However, a significant challenge still exists improving catalytic activities, retarding practical applications. Herein, this article presents through application human self‐driven triboelectric device impose electrical stimulus, multiple enzyme‐like activities single‐atom copper nanozyme (Cu‐NC) remarkably improved, thereby boosting cancer cell oxidative damage and death realizing improved therapy. Under an stimulus with 20 V voltage, peroxidase, catalase, oxidase, glutathione oxidase like Cu‐NC all boost generation free radicals. Through calculation, work analyzes how modulates activity via decreasing adsorption energy H 2 O on Cu sites, increasing d xy orbital near Fermi level, shifting d‐band center Cu, facilitating reactions. This opens new perspectives nanoenzymes
Language: Английский
Citations
51Nature Communications, Journal Year: 2024, Volume and Issue: 15(1)
Published: Jan. 11, 2024
Abstract Emerging evidence indicates that the activation of ferroptosis by glutathione peroxidase 4 (GPX4) inhibitors may be a prominent therapeutic strategy for tumor suppression. However, wide application GPX4 in therapy is hampered due to poor delivery efficacy and nonspecific ferroptosis. Taking advantage vivo self-assembly, we develop peptide-ferriporphyrin conjugate with microenvironment specific improve penetration, endocytosis inhibition, ultimately enhancing its anticancer activity via Briefly, inhibitory peptide conjugated an assembled linker decorated pH-sensitive moiety ferriporphyrin produce ( Gi-F-CAA ). Under acidic tumor, self-assembles into large nanoparticles (Gi-F) enhanced hydrophobic interaction after hydrolysis CAA, improving efficiency. Importantly, Gi-F exhibits substantial inhibition assembly binding AEB ) effect, augmenting oxidative stress ferriporphyrin-based Fenton reaction, enabling antitumor properties multiple models. Our findings suggest this design effect can induction ferroptosis, providing alternative overcoming chemoresistance.
Language: Английский
Citations
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