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Cuproptosis: Cellular and molecular mechanisms underlying copper-induced cell death
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.cell.2012.03.042openalex-snapshot
Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death
inferredcites →https://doi.org/10.1021/acschembio.0c00900openalex-snapshot
Protein Folding Stability Changes Across the Proteome Reveal Targets of Cu Toxicity in E. coli
inferredcites →https://doi.org/10.1038/s41568-021-00417-2openalex-snapshot
Connecting copper and cancer: from transition metal signalling to metalloplasia
inferredcites →https://doi.org/10.1038/s41589-019-0291-9openalex-snapshot
Mitochondrial metabolism promotes adaptation to proteotoxic stress
inferredcites →https://doi.org/10.1053/j.gastro.2018.11.032openalex-snapshot
Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis
inferredcites →https://doi.org/10.1126/science.aaz8899openalex-snapshot
Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice
inferredcites →https://doi.org/10.1126/science.aba8740openalex-snapshot
The histone H3-H4 tetramer is a copper reductase enzyme
inferredcites →https://doi.org/10.1126/science.abf0529openalex-snapshot
Copper induces cell death by targeting lipoylated TCA cycle proteins
inferredcites →https://doi.org/10.1146/annurev.genom.1.1.75openalex-snapshot
Iron Metabolism: Iron Deficiency and Iron Overload
inferredcites →https://doi.org/10.7554/elife.64690openalex-snapshot
Mitochondrial copper and phosphate transporter specificity was defined early in the evolution of eukaryotes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4643724openalex-extracted
Synthesis and Anti-Cancer Investigations of Novel Copper(II) Complexes Based on Adenine
inferred← citeshttps://doi.org/10.1002/adfm.202405383openalex-snapshot
Engineered‐Doping Strategy for Self‐Sufficient Reactive Oxygen Species Blossom to Amplify Ferroptosis/Cuproptosis Sensibilization in Hepatocellular Carcinoma Treatment
inferred← citeshttps://doi.org/10.1002/adhm.202202949openalex-snapshot
Tumor Microenvironment Responsive Hollow Nanoplatform for Triple Amplification of Oxidative Stress to Enhance Cuproptosis‐Based Synergistic Cancer Therapy
inferred← citeshttps://doi.org/10.1002/adhm.202300410openalex-snapshot
Multifaceted Roles of Copper Ions in Anticancer Nanomedicine
inferred← citeshttps://doi.org/10.1002/adhm.202301429openalex-snapshot
DNAzyme‐Mediated Cascade Nanoreactor for Cuproptosis‐Promoted Pancreatic Cancer Synergistic Therapy
inferred← citeshttps://doi.org/10.1002/adhm.202401078openalex-snapshot
Human Serum Albumin Mediated Controllable Synthesis of Defect‐Rich Copper Hydroxide Nanowire for Cuproptosis‐Based Anti‐Tumor Therapy
inferred← citeshttps://doi.org/10.1002/adhm.71530openalex-snapshot
Engineering ZCIF@GSK Nanoplatform to Overcome Tumor Metabolism: LDHA Inhibition‐Mediated Cuproptosis for Highly Efficient Oncotherapy
inferred← citeshttps://doi.org/10.1002/adma.202212267openalex-snapshot
Cuproptosis Induced by ROS Responsive Nanoparticles with Elesclomol and Copper Combined with αPD‐L1 for Enhanced Cancer Immunotherapy
inferred← citeshttps://doi.org/10.1002/adma.202303432openalex-snapshot
Biofilm Microenvironment‐Responsive Self‐Assembly Nanoreactors for All‐Stage Biofilm Associated Infection through Bacterial Cuproptosis‐like Death and Macrophage Re‐Rousing
inferred← citeshttps://doi.org/10.1002/adma.202404971openalex-snapshot
Glutathione‐Scavenging Celastrol‐Cu Nanoparticles Induce Self‐Amplified Cuproptosis for Augmented Cancer Immunotherapy
inferred← citeshttps://doi.org/10.1002/adma.202506119openalex-snapshot
Cuproptosis to Cuproptosis‐Like: Therapeutic Strategies for Bacterial Infection
inferred← citeshttps://doi.org/10.1002/adtp.202400426openalex-snapshot
The Role of Copper Ions in Mediating the Anti‐Cancer Effects Using Nanomaterials
inferred← citeshttps://doi.org/10.1002/advs.202402516openalex-snapshot
Carrier‐Free Self‐Assembly Nano‐Sonosensitizers for Sonodynamic‐Amplified Cuproptosis‐Ferroptosis in Glioblastoma Therapy
inferred← citeshttps://doi.org/10.1002/advs.202501974openalex-snapshot
Navigating Transition Metal‐Dependent Cell Death: Mechanisms, Crosstalk, and Future Directions
inferred← citeshttps://doi.org/10.1002/advs.202521183openalex-snapshot
Dual‐Targeting Cuproptosis and Mitophagy via a Flavopiridol‐Copper Nanoplatform Potentiates Immunotherapy Against Uveal Melanoma
inferred← citeshttps://doi.org/10.1002/biof.70024openalex-snapshot
Targeting Cellular Energetics via Ferroptosis Mediated Cell Death in Resistant Colorectal Cancer Stem Cells
inferred← citeshttps://doi.org/10.1002/cam4.5214openalex-snapshot
Construction of a cuproptosis‐related lncRNA signature for predicting prognosis and immune landscape in osteosarcoma patients
inferred← citeshttps://doi.org/10.1002/cam4.6763openalex-snapshot
Cuproptosis gene‐related, neural network‐based prognosis prediction and drug‐target prediction for KIRC
inferred← citeshttps://doi.org/10.1002/cam4.7379openalex-snapshot
Identification of PSMD11 as a novel cuproptosis‐ and immune‐related prognostic biomarker promoting lung adenocarcinoma progression
inferred← citeshttps://doi.org/10.1002/imt2.70141openalex-snapshot
Metal‐dependent regulated cell death: Molecular architecture and translational frontiers
inferred← citeshttps://doi.org/10.1002/jat.4908openalex-snapshot
Role of DLAT‐Mediated Neuron Cuproptosis in Cognitive Impairment Induced by Lead Exposure
inferred← citeshttps://doi.org/10.1002/jbt.70807openalex-snapshot
Progress in the Research of Cuproptosis and Possible Targets for Gynecological Cancers
inferred← citeshttps://doi.org/10.1002/jcla.24723openalex-snapshot
Prognostic prediction of head and neck squamous cell carcinoma: Construction of cuproptosis‐related long non‐coding RNA signature
inferred← citeshttps://doi.org/10.1002/jsp2.70080openalex-snapshot
Crosstalk Between Ferroptosis and Cuproptosis in Intervertebral Disc Degeneration: Mechanisms, Therapeutic Targets, and Future Directions
inferred← citeshttps://doi.org/10.1002/mba2.36openalex-snapshot
Nanotechnology connecting copper metabolism and tumor therapy
inferred← citeshttps://doi.org/10.1002/mco2.70244openalex-snapshot
Mitochondria as Regulators of Nonapoptotic Cell Death in Cancer
inferred← citeshttps://doi.org/10.1002/pros.70049openalex-snapshot
LIAS Promotes Cuproptosis in Prostate Cancer Cells by Suppressing Glycolysis via the p53 Signaling Pathway
inferred← citeshttps://doi.org/10.1002/smll.202406802openalex-snapshot
In Situ Transformable Fibrillar Clusters Disrupt Intracellular Copper Metabolic Homeostasis by Comprehensive Blockage of Cuprous Ions Efflux
inferred← citeshttps://doi.org/10.1002/smll.202412462openalex-snapshot
Nanomaterial‐Triggered Ferroptosis and Cuproptosis in Cancer Therapy
inferred← citeshttps://doi.org/10.1002/smll.202501259openalex-snapshot
Oligocopper‐Loaded Lipoic Acid Nanoparticles Promote Mitochondrial Protein Lipoylation for Augmented Cuproptosis Therapy
inferred← citeshttps://doi.org/10.1007/s00210-023-02928-1openalex-snapshot
PDE3B regulates KRT6B and increases the sensitivity of bladder cancer cells to copper ionophores
inferred← citeshttps://doi.org/10.1007/s00210-025-04497-xopenalex-snapshot
Targeting cuproptosis opens a new chapter of nanomedicine: a scientometric and graphical analysis
inferred← citeshttps://doi.org/10.1007/s00277-024-05841-6openalex-snapshot
Exploring and clinical validation of prognostic significance and therapeutic implications of copper homeostasis-related gene dysregulation in acute myeloid leukemia
inferred← citeshttps://doi.org/10.1007/s00432-023-05005-5openalex-snapshot
A risk prognostic model for patients with esophageal squamous cell carcinoma basing on cuproptosis and ferroptosis
inferred← citeshttps://doi.org/10.1007/s00775-026-02175-8openalex-snapshot
Cuproptosis and the bioinorganic basis of copper-induced cell death
inferred← citeshttps://doi.org/10.1007/s10142-023-01114-zopenalex-snapshot
Gene body hypomethylation of pyroptosis-related genes NLRP7, NLRP2, and NLRP3 facilitate non-invasive surveillance of hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s10142-025-01552-xopenalex-snapshot
Aberrant DNA methylation as a key modulator of cell death pathways: insights into cancer progression and other diseases
inferred← citeshttps://doi.org/10.1007/s10238-024-01491-0openalex-snapshot
lncRNAs as prognostic markers and therapeutic targets in cuproptosis-mediated cancer
inferred← citeshttps://doi.org/10.1007/s10495-022-01790-5openalex-snapshot
Cuproptosis-related LncRNA signatures as a prognostic model for head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.1007/s10495-023-01851-3openalex-snapshot
Advances in tumor nanotechnology: theragnostic implications in tumors via targeting regulated cell death
inferred← citeshttps://doi.org/10.1007/s10495-023-01927-0openalex-snapshot
From ferroptosis to cuproptosis, and calcicoptosis, to find more novel metals-mediated distinct form of regulated cell death
inferred← citeshttps://doi.org/10.1007/s10495-023-01928-zopenalex-snapshot
Ferroptosis and cuproptposis in kidney Diseases: dysfunction of cell metabolism
inferred← citeshttps://doi.org/10.1007/s10495-024-01993-yopenalex-snapshot
Cuproptosis and Cu: a new paradigm in cellular death and their role in non-cancerous diseases
inferred← citeshttps://doi.org/10.1007/s10495-024-02002-yopenalex-snapshot
Sphingolipid metabolism and regulated cell death in malignant melanoma
inferred← citeshttps://doi.org/10.1007/s10495-025-02090-4openalex-snapshot
Novel impact of metal ion-induced cell death on diabetic cardiomyopathy pathogenesis and therapy
inferred← citeshttps://doi.org/10.1007/s10495-026-02342-xopenalex-snapshot
Single-cell profiling and machine learning identify cuproptosis-related fibroblast subpopulations and fibrogenesis modulator AEBP1 in endometriosis
inferred← citeshttps://doi.org/10.1007/s10495-026-02416-wopenalex-snapshot
Metabolic cell death: ferroptosis, cuproptosis, and disulfidptosis as a unified framework for targeting metabolic vulnerabilities in disease
inferred← citeshttps://doi.org/10.1007/s10528-024-10784-8openalex-snapshot
Cuproptosis-Related Gene FDX1 Suppresses the Growth and Progression of Colorectal Cancer by Retarding EMT Progress
inferred← citeshttps://doi.org/10.1007/s10620-025-09137-1openalex-snapshot
PDHA1 Orchestrates Hepatocellular Carcinoma Progression Through LINC00607-Mediated Regulation of Cuproptosis and Immune Evasion
inferred← citeshttps://doi.org/10.1007/s10815-024-03256-wopenalex-snapshot
Blocking lactate regulation of the Grhl2/SLC31A1 axis inhibits trophoblast cuproptosis and preeclampsia development
inferred← citeshttps://doi.org/10.1007/s10895-024-03587-yopenalex-snapshot
Recent Development on Copper-Sensor and its Biological Applications: A Review
inferred← citeshttps://doi.org/10.1007/s11010-026-05604-zopenalex-snapshot
Deciphering the interplay between cuproptosis and mitochondrial energy metabolism in thyroid cancer: a multi-omics study for molecular subtyping, prognosis, and tumor microenvironment characterization
inferred← citeshttps://doi.org/10.1007/s11064-023-03962-4openalex-snapshot
Research Advances of Mitochondrial Dysfunction in Perioperative Neurocognitive Disorders
inferred← citeshttps://doi.org/10.1007/s11596-024-2832-zopenalex-snapshot
Copper Metabolism and Cuproptosis: Molecular Mechanisms and Therapeutic Perspectives in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/s12010-026-05726-6openalex-snapshot
Licochalcone a Disrupted Mitochondrial Function to Promote Cuproptosis in Glioblastoma Through Regulating RAS/MAPK Pathway
inferred← citeshttps://doi.org/10.1007/s12011-023-03668-2openalex-snapshot
Cuproptosis Regulates Microenvironment and Affects Prognosis in Prostate Cancer
inferred← citeshttps://doi.org/10.1007/s12011-024-04440-wopenalex-snapshot
Copper Dysmetabolism is Connected to Epithelial-Mesenchymal Transition: A Pilot Study in Colorectal Cancer Patients
inferred← citeshttps://doi.org/10.1007/s12032-026-03298-3openalex-snapshot
Metabolic vulnerabilities in advanced prostate cancer: the interplay of ferroptosis, cuproptosis, and the inflammatory microenvironment
inferred← citeshttps://doi.org/10.1007/s12035-023-03565-8openalex-snapshot
Identification of Key Genes and Immunological Features Associated with Copper Metabolism in Parkinson’s Disease by Bioinformatics Analysis
inferred← citeshttps://doi.org/10.1007/s12035-024-04188-3openalex-snapshot
Crosstalk Between Cell Death and Spinal Cord Injury: Neurology and Therapy
inferred← citeshttps://doi.org/10.1007/s12672-024-00964-8openalex-snapshot
A combination of cuproptosis and lncRNAs predicts the prognosis and tumor immune microenvironment in cervical cancer
inferred← citeshttps://doi.org/10.1007/s12672-025-03150-6openalex-snapshot
Exploring the synergetic role of cuproptosis and ferroptosis and their implication in advancing cancer therapeutics
inferred← citeshttps://doi.org/10.1007/s12672-025-04311-3openalex-snapshot
Cuproptosis-related gene DLD expression correlates with the prognosis and tumor immune microenvironment in clear cell renal cell carcinoma
inferred← citeshttps://doi.org/10.1007/s12672-026-04645-6openalex-snapshot
The impact of lipid metabolism remodeling in the tumor microenvironment on angiogenesis
inferred← citeshttps://doi.org/10.1007/s13258-023-01406-5openalex-snapshot
Identification of a novel prognostic signature composed of 3 cuproptosis-related transcription factors in colon adenocarcinoma
inferred← citeshttps://doi.org/10.1016/bs.mcb.2026.02.002openalex-snapshot
Fluorogenic probes for intracellular copper detection and the study of cuproptosis
inferred← citeshttps://doi.org/10.1016/j.apsb.2025.02.022openalex-snapshot
Bioactive metallic nanoparticles for synergistic cancer immunotherapy
inferred← citeshttps://doi.org/10.1016/j.bbadis.2026.168375openalex-snapshot
LINC02207 suppresses breast cancer progression by promoting cuproptosis through NFAT5 regulation
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130872openalex-snapshot
The CEBPA/FDX1 axis elevates sensitivity to cuproptosis in lung adenocarcinoma cells
inferred← citeshttps://doi.org/10.1016/j.bbcan.2024.189180openalex-snapshot
Unveiling Cuproptosis: Mechanistic insights, roles, and leading advances in oncology
inferred← citeshttps://doi.org/10.1016/j.bbcan.2026.189591openalex-snapshot
Targeting mitochondria in triple-negative breast cancer: Emerging therapeutic and drug development strategies
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150926openalex-snapshot
Overexpression of MCL1 attenuates irritable bowel syndrome by regulating cuproptosis: Screening and validation
inferred← citeshttps://doi.org/10.1016/j.bcp.2026.117769openalex-snapshot
Iron homeostasis and ferroptosis: a converging axis in cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2025.123893openalex-snapshot
Programmable bacteria-driven biohybrid triggers spatiotemporal-controlled STING activation to potentiate cuproptosis-based cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2026.124373openalex-snapshot
A biocompatible copper based therapeutic nanoplatform for CD44 specific tumor targeted therapy and potent immune reprogramming
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114301openalex-snapshot
4-Octyl itaconate inhibits aerobic glycolysis by targeting GAPDH to promote cuproptosis in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114883openalex-snapshot
Novel targets for gastric cancer: The tumor microenvironment (TME), N6-methyladenosine (m6A), pyroptosis, autophagy, ferroptosis and cuproptosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115730openalex-snapshot
Copper-mediated novel cell death pathway in tumor cells and implications for innovative cancer therapies
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115839openalex-snapshot
Copper homeostasis and copper-induced cell death： Novel targeting for intervention in the pathogenesis of vascular aging
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.116115openalex-snapshot
Crosstalk between ferroptosis and cuproptosis: From mechanism to potential clinical application
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116247openalex-snapshot
The effect of lipid metabolism on cuproptosis-inducing cancer therapy
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116585openalex-snapshot
Elucidating cuproptosis in metabolic dysfunction-associated steatotic liver disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117182openalex-snapshot
Focus on cuproptosis: Exploring new mechanisms and therapeutic application prospects of cuproptosis regulation
inferred← citeshttps://doi.org/10.1016/j.biopha.2025.117814openalex-snapshot
Cuproptosis and copper as potential mechanisms and intervention targets in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118422openalex-snapshot
Cuproptosis: Current insights into its multifaceted role in disease, cancer, and translational/therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.bjorl.2025.101560openalex-snapshot
The important role of cuproptosis and cuproptosis-related genes in the development of thyroid carcinoma revealed by transcriptomic analysis and experiments
inferred← citeshttps://doi.org/10.1016/j.cbi.2024.110943openalex-snapshot
The copper transporter, SLC31A1, transcriptionally activated by ELF3, imbalances copper homeostasis to exacerbate cisplatin-induced acute kidney injury through mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1016/j.ccr.2025.217368openalex-snapshot
Antibacterial biomaterials: disruption of antibiotic tolerance for resistance prevention
inferred← citeshttps://doi.org/10.1016/j.ccr.2026.218139openalex-snapshot
Disulfidptosis-based nanomedicines for targeting tumor metabolic vulnerabilities
inferred← citeshttps://doi.org/10.1016/j.cej.2025.165766openalex-snapshot
Biomimetic Ti3C2 nanosheets for synergistically overcoming chemoresistance and boosting immunotherapy via enhanced cuproptosis in cancer
inferred← citeshttps://doi.org/10.1016/j.cej.2025.167168openalex-snapshot
Targeting the mitochondrial-autophagy axis in pituitary neuroendocrine tumors via intracellular copper overload
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111565openalex-snapshot
Kynureninase induce cuproptosis resistance in gastric cancer progression through downregulating lipotic acid synthetase mediated non-canonical mechanism
inferred← citeshttps://doi.org/10.1016/j.clim.2025.110617openalex-snapshot
Plasma anti-ATP7A/B autoantibodies as potential biomarkers for the detection and prognosis of non-small cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.clim.2026.110764openalex-snapshot
Plasma anti-ATP7A/ATP7B/COPT1 autoantibodies as potential biomarkers for breast cancer detection
inferred← citeshttps://doi.org/10.1016/j.clinsp.2024.100410openalex-snapshot
Identification of potential crucial cuproptosis-related genes in myocardial ischemia-reperfusion injury through the bioinformatic analysis
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2024.114196openalex-snapshot
Cu0-based nanoparticles boost anti-tumor efficacy via synergy of cuproptosis and ferroptosis enhanced by cuproptosis-induced glutathione synthesis disorder
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2025.114682openalex-snapshot
Multi-pathway copper metabolisms regulation based on an engineered copper/ferrous nanoplatform for enhanced tumor cuproptosis therapy
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2026.115415openalex-snapshot
Multifunctional nanozyme-mediated synergistic activation of cuproptosis, ferroptosis, and pyroptosis for potent antitumor therapy
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2026.115824openalex-snapshot
PDGF receptor-β-targeted copper-zinc nanozyme interfered glycolysis and remodelled tumor microenvironment for enhanced cuproptosis of lung cancer
inferred← citeshttps://doi.org/10.1016/j.crbiot.2024.100253openalex-snapshot
Identification of a prognostic model based on cuproptosis and ferroptosis-related genes in patients with head and neck squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2026.105296openalex-snapshot
Cuproptosis: Bridging targeted therapy and immunotherapy in cancer treatment
inferred← citeshttps://doi.org/10.1016/j.drudis.2024.104104openalex-snapshot
Innovative Strategies in Cancer Treatment: Harnessing Cuproptosis and Nanotechnology for Targeted Therapy
inferred← citeshttps://doi.org/10.1016/j.drup.2023.101018openalex-snapshot
Cuproptosis: A novel therapeutic target for overcoming cancer drug resistance
inferred← citeshttps://doi.org/10.1016/j.ejphar.2025.178085openalex-snapshot
The emerging role of disulfidptosis in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.122554openalex-snapshot
Growth retardation and suppression of ubiquitin-dependent catabolic processes in the brackish water clam Corbicula japonica in response to salinity changes and bioaccumulation of toxic heavy metals
inferred← citeshttps://doi.org/10.1016/j.fct.2026.116147openalex-snapshot
Multi-omics reveals PM2.5-Associated neuronal disulfidptosis: SLC3A2-OXSM imbalance, immune dysregulation, and electrophysiological dysfunction
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.06.017openalex-snapshot
Phillygenin ameliorates myocardial ischemia-reperfusion injury by inhibiting cuproptosis via the autophagy-lysosome degradation of CTR1
inferred← citeshttps://doi.org/10.1016/j.hazadv.2025.100788openalex-snapshot
Understanding cuproptosis through FDX1-mediated lipoylation and proteotoxic stress in Channa punctatus
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e13456openalex-snapshot
A combined analysis of bulk and single-cell sequencing data reveals metabolic enzyme, pyruvate dehydrogenase E1 subunit beta (PDHB), as a prediction biomarker for the tumor immune response and immunotherapy
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e14091openalex-snapshot
The multi-omics analysis identifies a novel cuproptosis-anoikis-related gene signature in prognosis and immune infiltration characterization of lung adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e17582openalex-snapshot
Dual identity of tumor-associated macrophage in regulated cell death and oncotherapy
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e19352openalex-snapshot
A cuproptosis-related lncRNA signature for predicting prognosis and immune response in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21506openalex-snapshot
Integrated analysis reveals a potential cuproptosis-related ceRNA axis SNHG17/miR-29a-3p/GCSH in prostate adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e26759openalex-snapshot
Identification and immunological role of cuproptosis in osteoporosis
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e32480openalex-snapshot
Programmed cell death, from liver Ischemia–Reperfusion injury perspective: An overview
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e34011openalex-snapshot
The role of cuproptosis-related genes in pan-cancer and the development of cuproptosis-related risk model in colon adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.identj.2026.109506openalex-snapshot
MT2A-Mediated Regulation of Cuproptosis in Human Dental Pulp Cells Modulates Macrophage M1 Polarization in Pulpitis
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.132029openalex-snapshot
Cu–Tremella fuciformis polysaccharide–based tumor microenvironment–responsive injectable gels for cuproptosis-based synergistic osteosarcoma therapy
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.134238openalex-snapshot
Mesoporous polydopamine/copper sulfide hybrid nanocomposite for highly efficient NIR-triggered bacterial inactivation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.136090openalex-snapshot
Bovine serum albumin-bound homologous targeted nanoparticles for breast cancer combinatorial therapy
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2023.123622openalex-snapshot
Metal-based nanoparticles in cancer therapy: Exploring photodynamic therapy and its interplay with regulated cell death pathways
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115446openalex-snapshot
Clinical application of copper needle therapy in venous malformation: mechanistic insights from cuproptosis and comparative clinical efficacy
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110804openalex-snapshot
Identification of immunological characteristics and cuproptosis-related molecular clusters in Rheumatoid arthritis
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113698openalex-snapshot
Copper homeostasis and Cuprotosis: Exploring novel therapeutic strategies for connective tissue diseases
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114967openalex-snapshot
Mycobacterium tuberculosis stimulates cuproptosis by regulating Lnc-Gm5532 to target FDX1 for bacteria intracellular survival
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115468openalex-snapshot
Knockdown of LOXL2 suppresses cuproptosis induced by H2O2 to inhibited the procession of ulcerative colitis
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115788openalex-snapshot
Cuproptosis as a regulator in human diseases: From basic mechanisms to clinical relevance
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.116040openalex-snapshot
The mechanism of CISD3 regulating NRF2-ATP7B to ameliorate alcohol-induced liver mitochondrial dysfunction and cuproptosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.116132openalex-snapshot
Harnessing tumor cell death mechanisms to reshape the immune microenvironment: A novel approach for head and neck cancer therapy
inferred← citeshttps://doi.org/10.1016/j.intimp.2026.117332openalex-snapshot
Vitamin D receptor regulates macrophage polarization and cuproptosis via transcriptional activation of ATP7B to mitigate intrauterine adhesion fibrosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2026.117419openalex-snapshot
Cuproptosis in age-related orthopedic diseases: mechanisms and therapeutic prospects
inferred← citeshttps://doi.org/10.1016/j.jceh.2026.103675openalex-snapshot
The ncRNA–Epigenetic–Cuproptosis Axis in Liver Diseases: From Copper Homeostasis to Precision Hepatology
inferred← citeshttps://doi.org/10.1016/j.jcis.2025.137421openalex-snapshot
Dual-upregulation of p53 for self-sensitized cuproptosis via microwave dynamic and NO gas therapy
inferred← citeshttps://doi.org/10.1016/j.jep.2026.121359openalex-snapshot
Polygonatum Sibiricum polysaccharide ameliorates Alzheimer's disease by alleviating cuproptosis and activating the PI3K/AKT signaling pathway
inferred← citeshttps://doi.org/10.1016/j.jgeb.2023.100338openalex-snapshot
Identification of cuproptosis-related lncRNAs signature for predicting the prognosis in patients with kidney renal clear cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138403openalex-snapshot
Cu(OH)2 nanopesticide induced liver dysfunction in mice by targeting lipoylated tricarboxylic acid cycle proteins via ferredoxin 1
inferred← citeshttps://doi.org/10.1016/j.jncc.2025.02.007openalex-snapshot
Revealing the landscape of targeting mitochondrial functions and behaviors to overcome cancer chemoresistance
inferred← citeshttps://doi.org/10.1016/j.jpha.2025.101500openalex-snapshot
Cuproptosis tracker: Visualizing organelle dynamics with a dual-targeted fluorescent probe
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.122223openalex-snapshot
Copper homeostasis and cuproptosis in mitochondria
inferred← citeshttps://doi.org/10.1016/j.matdes.2026.116489openalex-snapshot
Redox-responsive copper-based nanoplatform enables efficient pancreatic ductal adenocarcinoma therapy via icaritin-enhanced cuproptosis
inferred← citeshttps://doi.org/10.1016/j.medengphy.2025.104427openalex-snapshot
Research advances, challenges and outlooks of copper-containing scaffolds derived from 3D printing for tissue repair
inferred← citeshttps://doi.org/10.1016/j.mito.2023.08.002openalex-snapshot
Epilepsy: Mitochondrial connections to the ‘Sacred’ disease
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138836openalex-snapshot
Synthesis and anti-cancer investigations of copper(II) complexes based on adenine
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146498openalex-snapshot
Natural thymol-derived chemosensor for selective visual detection of Cu(II) and Fe(III) ions
inferred← citeshttps://doi.org/10.1016/j.mtbio.2024.101300openalex-snapshot
Cuprorivaite microspheres inhibit cuproptosis and oxidative stress in osteoarthritis via Wnt/β-catenin pathway
inferred← citeshttps://doi.org/10.1016/j.mtbio.2024.101326openalex-snapshot
Orchestrated copper-loaded nanoreactor for simultaneous induction of cuproptosis and immunotherapeutic intervention in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.mtbio.2025.101894openalex-snapshot
Cuproptosis-driven nanostrategies: Synergistic nanoplatforms for tumor microenvironment reprogramming and enhanced anticancer efficacy
inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103325openalex-snapshot
Biomimetic self-assembled copper nanoadjuvant potentiates hepatocellular carcinoma immunotherapy via cuproptosis-driven cGAS-STING activation
inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103365openalex-snapshot
DNA-damage-targeting copper nanoparticles induce cuproptosis for enhanced cancer radiotherapy
inferred← citeshttps://doi.org/10.1016/j.mtbio.2026.103508openalex-snapshot
Lactate metabolism regulation enhances cuproptosis to activate antitumor immunity: Synergistic therapy of hyaluronic acid nanomicelles delivering lactate oxidase/copper-doped carbon dots combined with α-PD-L1 inhibits distant tumors
inferred← citeshttps://doi.org/10.1016/j.mtchem.2025.102877openalex-snapshot
In situ disulfiram toxification synergizes Au–Pt nanozymes to amplify cuproptosis to enhance hepatocellular carcinoma chemotherapy and immunotherapy
inferred← citeshttps://doi.org/10.1016/j.nantod.2024.102608openalex-snapshot
Disruption of self-protection pathways enables endogenous copper-evoked cuproptosis via bioorthogonal nanoblocker
inferred← citeshttps://doi.org/10.1016/j.nantod.2025.102701openalex-snapshot
Boosting cuproptosis by activating JAK-STAT signaling pathway and synergrtic with interface-enhanced sonodynamic immunotherapy against cancer
inferred← citeshttps://doi.org/10.1016/j.nbd.2025.106789openalex-snapshot
Identifying disulfidptosis-related biomarkers in epilepsy based on integrated bioinformatics and experimental analyses
inferred← citeshttps://doi.org/10.1016/j.nbd.2025.106974openalex-snapshot
A primer on copper biology in the brain
inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107264openalex-snapshot
Copper metabolism and its role in diabetic complications: A review
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108442openalex-snapshot
Neural–metabolic crosstalk governing cell death and therapy resistance in tumors
inferred← citeshttps://doi.org/10.1016/j.pmatsci.2023.101145openalex-snapshot
The copper age in cancer treatment: From copper metabolism to cuproptosis
inferred← citeshttps://doi.org/10.1016/j.preme.2026.100062openalex-snapshot
Nanomaterials for precise cuproptosis modulation: From molecular mechanisms to systemic therapeutics
inferred← citeshttps://doi.org/10.1016/j.prp.2026.156601openalex-snapshot
Cuproptosis-mediated metabolic–inflammatory coupling in hypertensive myocardial injury: Mechanistic insights and therapeutic perspectives
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103757openalex-snapshot
Hypoxia, cuproptosis, and osteoarthritis: Unraveling the molecular crosstalk
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.161458openalex-snapshot
Cuproptosis is involved in copper-induced hepatotoxicity in chickens
inferred← citeshttps://doi.org/10.1016/j.semcancer.2024.09.003openalex-snapshot
Interplay of ferroptosis, cuproptosis, and PANoptosis in cancer treatment-induced cardiotoxicity: Mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.taap.2025.117496openalex-snapshot
Copper ionophore enhanced cisplatin efficiency through DLAT-cuprotosis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2026.117974openalex-snapshot
Transcriptome and metabolome analysis reveals that cuproptosis in bovine cumulus cells triggers the intercellular transmission of senescence and mitochondrial dysfunction to impair oocyte quality
inferred← citeshttps://doi.org/10.1016/j.tips.2023.07.004openalex-snapshot
Copper homeostasis and cuproptosis in cardiovascular disease therapeutics
inferred← citeshttps://doi.org/10.1016/j.tox.2025.154298openalex-snapshot
Copper exposure induces autophagy and angiogenesis in liver cell via ATF4 activation independent of TFEB
inferred← citeshttps://doi.org/10.1016/j.tranon.2026.102724openalex-snapshot
SNHG7 interacts with PCBP2 to promote CDKN2A expression and modulate cuproptosis in colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.yjpso.2023.100082openalex-snapshot
WITHDRAWN: Identification and immunological characterization of cuproptosis-related molecular clusters in biliary atresia
inferred← citeshttps://doi.org/10.1016/j.ymthe.2025.09.004openalex-snapshot
Elesclomol-copper combination synergistically targets mitochondrial metabolism in cancer stem cells to overcome chemoresistance in PDAC
inferred← citeshttps://doi.org/10.1021/acs.accounts.2c00643openalex-snapshot
Fluorescent Probes for Biological Species and Microenvironments: from Rational Design to Bioimaging Applications
inferred← citeshttps://doi.org/10.1021/acs.analchem.6c03779openalex-snapshot
Targeted Lifetime Probe Enables Quantitative FLIM Mapping of Lipid Droplet Polarity Remodeling under Copper-Induced Oxidative Stress
inferred← citeshttps://doi.org/10.1021/acsabm.4c01710openalex-snapshot
Ultrasound-Activated Copper Matrix Nanosonosensitizer for Cuproptosis-Based Synergy Therapy
inferred← citeshttps://doi.org/10.1021/acsami.5c01443openalex-snapshot
Theranostic Rhenium Complexes as Suborganelle-Targeted Copper Ionophores To Stimulate Cuproptosis for Cancer Immunotherapy
inferred← citeshttps://doi.org/10.1021/acsami.5c25733openalex-snapshot
Fucoidan-Copper Nanoparticles to Potentiate Cancer Cell Cuproptosis and Tumor Immune Microenvironment Enhancement
inferred← citeshttps://doi.org/10.1021/acscentsci.4c02188openalex-snapshot
Discovery of Natural Resorcylic Acid Lactones as Novel Potent Copper Ionophores Covalently Targeting PRDX1 to Induce Cuproptosis for Triple-Negative Breast Cancer Therapy
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.2c00601openalex-snapshot
Surface Membrane Coating as a Versatile Platform for Modifying Antitumor Nanoparticles
inferred← citeshttps://doi.org/10.1021/acsmaterialslett.5c00711openalex-snapshot
Cuproptosis: An Emerging Cell Death Modality for Antitumor Therapy
inferred← citeshttps://doi.org/10.1021/acsnano.3c12796openalex-snapshot
Microfluidic Synthesis of CuH Nanoparticles for Antitumor Therapy through Hydrogen-Enhanced Apoptosis and Cuproptosis
inferred← citeshttps://doi.org/10.1021/acsnano.5c19675openalex-snapshot
Self-Carrier Nanoagonist Enabling Positive Feedback Regulation of Cuproptosis-Immunity for Potent Antitumor Therapy
inferred← citeshttps://doi.org/10.1021/acsnanomed.6c00136openalex-snapshot
Nano-Radiosensitizers for Radiotherapy: Design Strategies and Antitumor Immune Responses
inferred← citeshttps://doi.org/10.1021/acsomega.2c07052openalex-snapshot
Cuproptosis-Mediated Patterns Characterized by Distinct Tumor Microenvironment and Predicted the Immunotherapy Response for Gastric Cancer
inferred← citeshttps://doi.org/10.1021/jacs.3c14247openalex-snapshot
Enzyme Core Spherical Nucleic Acid That Enables Enhanced Cuproptosis and Antitumor Immune Response through Alleviating Tumor Hypoxia
inferred← citeshttps://doi.org/10.1038/s41388-025-03366-4openalex-snapshot
FDX1 promotes elesclomol-induced PANoptosis in diffuse large B-cell lymphoma via activating IRF3/IFN-β signaling
inferred← citeshttps://doi.org/10.1038/s41388-026-03945-zopenalex-snapshot
Inhibition of PINK1/Parkin-mediated mitophagy enhances the susceptibility of breast cancer to cuproptosis
inferred← citeshttps://doi.org/10.1038/s41389-026-00621-5openalex-snapshot
Ubiquitin-specific protease 11 suppresses cuproptosis in colorectal cancer by regulating the ubiquitination and stability of ISCU
inferred← citeshttps://doi.org/10.1038/s41392-025-02140-yopenalex-snapshot
Phototherapy in cancer treatment: strategies and challenges
inferred← citeshttps://doi.org/10.1038/s41392-026-03043-2openalex-snapshot
Cuproptosis and ferroptosis: signal pathways, diseases and therapeutic targets
inferred← citeshttps://doi.org/10.1038/s41418-024-01341-2openalex-snapshot
Dysregulated Wnt/β-catenin signaling confers resistance to cuproptosis in cancer cells
inferred← citeshttps://doi.org/10.1038/s41419-023-05930-wopenalex-snapshot
Ferroptosis as a potential target for cancer therapy
inferred← citeshttps://doi.org/10.1038/s41565-024-01784-1openalex-snapshot
A cuproptosis nanocapsule for cancer radiotherapy
inferred← citeshttps://doi.org/10.1038/s41598-024-72664-wopenalex-snapshot
Machine learning predicts cuproptosis-related lncRNAs and survival in glioma patients
inferred← citeshttps://doi.org/10.1038/s41598-026-49929-7openalex-snapshot
CuAgent provides a RAG-assisted intelligent framework to investigate cuproptosis
inferred← citeshttps://doi.org/10.1038/s41598-026-58577-wopenalex-snapshot
A multi-programmed cell death-related LncRNA signature for prognosis and immune microenvironment evaluation in kidney renal clear cell carcinoma
inferred← citeshttps://doi.org/10.1038/s42003-025-09201-6openalex-snapshot
TRIM21 promotes K63-linked ubiquitination of ALKBH5 and suppresses cuproptosis via down-regulation of LIAS in esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1038/s42003-025-09497-4openalex-snapshot
METTL3-mediated m6A modification of FDX1 confers resistance to cuproptosis and promotes hepatocellular carcinoma progression
inferred← citeshttps://doi.org/10.1039/d3tb02929hopenalex-snapshot
Unveiling the potential of HKUST-1: synthesis, activation, advantages and biomedical applications
inferred← citeshttps://doi.org/10.1039/d4cc06677dopenalex-snapshot
Elucidating cuproptosis-linked redox dynamics in Wilson's disease via a reversible ratiometric fluorescence strategy
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