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The Role of Macrophage Iron Overload and Ferroptosis in Atherosclerosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/biof.1803openalex-snapshot
Thyroid hormones inhibit apoptosis of macrophage induced by oxidized low‐density lipoprotein
inferredcites →https://doi.org/10.1002/cam4.1670openalex-snapshot
Iron overloaded polarizes macrophage to proinflammation phenotype through ROS /acetyl‐p53 pathway
inferredcites →https://doi.org/10.1002/eji.200939889openalex-snapshot
Differential regulation of iron homeostasis during human macrophage polarized activation
inferredcites →https://doi.org/10.1002/jcp.28518openalex-snapshot
Iron‐load exacerbates the severity of atherosclerosis via inducing inflammation and enhancing the glycolysis in macrophages
inferredcites →https://doi.org/10.1007/s12035-018-0961-8openalex-snapshot
Alterations in System xc− Expression in the Retina of Type 1 Diabetic Rats and the Role of Nrf2
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2018.09.037openalex-snapshot
CTRP5 promotes transcytosis and oxidative modification of low-density lipoprotein and the development of atherosclerosis
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2019.08.014openalex-snapshot
2019 ESC/EAS guidelines for the management of dyslipidaemias: Lipid modification to reduce cardiovascular risk
inferredcites →https://doi.org/10.1016/j.autrev.2012.03.003openalex-snapshot
Iron levels in polarized macrophages: Regulation of immunity and autoimmunity
inferredcites →https://doi.org/10.1016/j.bbadis.2016.03.004openalex-snapshot
Iron gene expression profile in atherogenic Mox macrophages
inferredcites →https://doi.org/10.1016/j.bbalip.2019.158531openalex-snapshot
Macrophage iron retention aggravates atherosclerosis: Evidence for the role of autocrine formation of hepcidin in plaque macrophages
inferredcites →https://doi.org/10.1016/j.bbrc.2013.10.115openalex-snapshot
SPION primes THP1 derived M2 macrophages towards M1-like macrophages
inferredcites →https://doi.org/10.1016/j.bbrc.2015.07.091openalex-snapshot
Low expression of ferroxidases is implicated in the iron retention in human atherosclerotic plaques
inferredcites →https://doi.org/10.1016/j.bbrc.2016.08.034openalex-snapshot
CISD1 inhibits ferroptosis by protection against mitochondrial lipid peroxidation
inferredcites →https://doi.org/10.1016/j.bbrc.2020.07.032openalex-snapshot
NEDD4L-mediated LTF protein degradation limits ferroptosis
inferredcites →https://doi.org/10.1016/j.bbrc.2021.05.011openalex-snapshot
SIRT1-autophagy axis inhibits excess iron-induced ferroptosis of foam cells and subsequently increases IL-1Β and IL-18
inferredcites →https://doi.org/10.1016/j.biocel.2006.02.006openalex-snapshot
Heat shock protein 27 downregulates the transferrin receptor 1-mediated iron uptake
inferredcites →https://doi.org/10.1016/j.biomaterials.2016.06.019openalex-snapshot
In vivo efficacy, toxicity and biodistribution of ultra-long circulating desferrioxamine based polymeric iron chelator
inferredcites →https://doi.org/10.1016/j.biopha.2022.112769openalex-snapshot
NOD1 splenic activation confers ferroptosis protection and reduces macrophage recruitment under pro-atherogenic conditions
inferredcites →https://doi.org/10.1016/j.canlet.2017.12.025openalex-snapshot
Heme oxygenase-1 mediates BAY 11–7085 induced ferroptosis
inferredcites →https://doi.org/10.1016/j.canlet.2018.06.018openalex-snapshot
CISD2 inhibition overcomes resistance to sulfasalazine-induced ferroptotic cell death in head and neck cancer
inferredcites →https://doi.org/10.1016/j.cell.2011.04.005openalex-snapshot
Macrophages in the Pathogenesis of Atherosclerosis
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/10.1016/j.cell.2017.09.021openalex-snapshot
Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease
inferredcites →https://doi.org/10.1016/j.cell.2019.04.024openalex-snapshot
The Coming Decade of Cell Death Research: Five Riddles
inferredcites →https://doi.org/10.1016/j.chembiol.2018.11.016openalex-snapshot
Exogenous Monounsaturated Fatty Acids Promote a Ferroptosis-Resistant Cell State
inferredcites →https://doi.org/10.1016/j.clim.2021.108872openalex-snapshot
Identification of critical ferroptosis regulators in lung adenocarcinoma that RRM2 facilitates tumor immune infiltration by inhibiting ferroptotic death
inferredcites →https://doi.org/10.1016/j.clinbiochem.2011.04.012openalex-snapshot
Analysis of the effects of iron and vitamin C co-supplementation on oxidative damage, antioxidant response and inflammation in THP-1 macrophages
inferredcites →https://doi.org/10.1016/j.devcel.2019.10.007openalex-snapshot
Prominin2 Drives Ferroptosis Resistance by Stimulating Iron Export
inferredcites →https://doi.org/10.1016/j.ebiom.2019.08.014openalex-snapshot
New insights into the role of iron in inflammation and atherosclerosis
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2020.07.026openalex-snapshot
Inhibition of ferroptosis alleviates atherosclerosis through attenuating lipid peroxidation and endothelial dysfunction in mouse aortic endothelial cell
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2021.05.009openalex-snapshot
Verification of ferroptosis and pyroptosis and identification of PTGS2 as the hub gene in human coronary artery atherosclerosis
inferredcites →https://doi.org/10.1016/j.imbio.2014.09.010openalex-snapshot
‘Ride on the ferrous wheel’ – The cycle of iron in macrophages in health and disease
inferredcites →https://doi.org/10.1016/j.jacc.2011.10.852openalex-snapshot
Hemoglobin Directs Macrophage Differentiation and Prevents Foam Cell Formation in Human Atherosclerotic Plaques
inferredcites →https://doi.org/10.1016/j.molcel.2015.06.011openalex-snapshot
Glutaminolysis and Transferrin Regulate Ferroptosis
inferredcites →https://doi.org/10.1016/j.redox.2020.101670openalex-snapshot
Hypoxia inhibits ferritinophagy, increases mitochondrial ferritin, and protects from ferroptosis
inferredcites →https://doi.org/10.1016/j.semcdb.2020.12.005openalex-snapshot
Iron in immune cell function and host defense
inferredcites →https://doi.org/10.1016/s1097-2765(01)00164-2openalex-snapshot
A PPARγ-LXR-ABCA1 Pathway in Macrophages Is Involved in Cholesterol Efflux and Atherogenesis
inferredcites →https://doi.org/10.1021/acs.nanolett.1c01401openalex-snapshot
Ferroptosis-Strengthened Metabolic and Inflammatory Regulation of Tumor-Associated Macrophages Provokes Potent Tumoricidal Activities
inferredcites →https://doi.org/10.1021/acscentsci.7b00589openalex-snapshot
Resolving the Role of Lipoxygenases in the Initiation and Execution of Ferroptosis
inferredcites →https://doi.org/10.1021/acscentsci.9b01063openalex-snapshot
GTP Cyclohydrolase 1/Tetrahydrobiopterin Counteract Ferroptosis through Lipid Remodeling
inferredcites →https://doi.org/10.1038/cddis.2016.208openalex-snapshot
Ferroptosis is induced following siramesine and lapatinib treatment of breast cancer cells
inferredcites →https://doi.org/10.1038/d41586-021-01203-8openalex-snapshot
A mitochondrial gatekeeper that helps cells escape death by ferroptosis
inferredcites →https://doi.org/10.1038/ncb3064openalex-snapshot
Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice
inferredcites →https://doi.org/10.1038/nri3520openalex-snapshot
Macrophages in atherosclerosis: a dynamic balance
inferredcites →https://doi.org/10.1038/onc.2015.32openalex-snapshot
HSPB1 as a novel regulator of ferroptotic cancer cell death
inferredcites →https://doi.org/10.1038/s41586-019-1705-2openalex-snapshot
The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis
inferredcites →https://doi.org/10.1038/s41586-021-03539-7openalex-snapshot
DHODH-mediated ferroptosis defence is a targetable vulnerability in cancer
inferredcites →https://doi.org/10.1038/s41589-019-0462-8openalex-snapshot
Redox lipid reprogramming commands susceptibility of macrophages and microglia to ferroptotic death
inferredcites →https://doi.org/10.1038/s41589-020-0472-6openalex-snapshot
Cytochrome P450 oxidoreductase contributes to phospholipid peroxidation in ferroptosis
inferredcites →https://doi.org/10.1039/d0bm01168aopenalex-snapshot
Cascade reaction-mediated efficient ferroptosis synergizes with immunomodulation for high-performance cancer therapy
inferredcites →https://doi.org/10.1042/cs20180067openalex-snapshot
Coronary artery disease in post-menopausal women: are there appropriate means of assessment?
inferredcites →https://doi.org/10.1074/jbc.ra119.009548openalex-snapshot
Ferroptosis is controlled by the coordinated transcriptional regulation of glutathione and labile iron metabolism by the transcription factor BACH1
inferredcites →https://doi.org/10.1093/eurheartj/ehz455openalex-snapshot
2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk
inferredcites →https://doi.org/10.1093/eurjpc/zwab154openalex-snapshot
2021 ESC Guidelines on cardiovascular disease prevention in clinical practice
inferredcites →https://doi.org/10.1097/fjc.0000000000001030openalex-snapshot
PDSS2 Inhibits the Ferroptosis of Vascular Endothelial Cells in Atherosclerosis by Activating Nrf2
inferredcites →https://doi.org/10.1126/sciadv.1600224openalex-snapshot
Targeting macrophage necroptosis for therapeutic and diagnostic interventions in atherosclerosis
inferredcites →https://doi.org/10.1155/2022/9304383openalex-snapshot
High Level of Uric Acid Promotes Atherosclerosis by Targeting NRF2‐Mediated Autophagy Dysfunction and Ferroptosis
inferredcites →https://doi.org/10.1161/atvbaha.118.312215openalex-snapshot
Hepcidin Deficiency Protects Against Atherosclerosis
inferredcites →https://doi.org/10.1161/atvbaha.119.312369openalex-snapshot
Ironing-Out the Role of Hepcidin in Atherosclerosis
inferredcites →https://doi.org/10.1172/jci155724openalex-snapshot
Erythroid lineage Jak2V617F expression promotes atherosclerosis through erythrophagocytosis and macrophage ferroptosis
inferredcites →https://doi.org/10.1172/jci44490openalex-snapshot
An unrestrained proinflammatory M1 macrophage population induced by iron impairs wound healing in humans and mice
inferredcites →https://doi.org/10.1172/jci93025openalex-snapshot
CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis
inferredcites →https://doi.org/10.1172/jci99032openalex-snapshot
Nano-targeted induction of dual ferroptotic mechanisms eradicates high-risk neuroblastoma
inferredcites →https://doi.org/10.1182/blood-2003-04-1250openalex-snapshot
Iron loading and erythrophagocytosis increase ferroportin 1 (FPN1) expression in J774 macrophages
inferredcites →https://doi.org/10.1182/blood-2017-12-822619openalex-snapshot
Increased erythrophagocytosis induces ferroptosis in red pulp macrophages in a mouse model of transfusion
inferredcites →https://doi.org/10.1186/s13578-020-00500-5openalex-snapshot
Iron accumulation in macrophages promotes the formation of foam cells and development of atherosclerosis
inferredcites →https://doi.org/10.1371/journal.pbio.2006203openalex-snapshot
Unsolved mysteries: How does lipid peroxidation cause ferroptosis?
inferredcites →https://doi.org/10.1371/journal.pone.0196921openalex-snapshot
Cell iron status influences macrophage polarization
inferredcites →https://doi.org/10.18632/aging.202660openalex-snapshot
Nicotine exacerbates atherosclerosis through a macrophage-mediated endothelial injury pathway
inferredcites →https://doi.org/10.2353/ajpath.2009.080431openalex-snapshot
Coronary Intraplaque Hemorrhage Evokes a Novel Atheroprotective Macrophage Phenotype
inferredcites →https://doi.org/10.3389/fcell.2020.590226openalex-snapshot
Iron Metabolism in Ferroptosis
inferredcites →https://doi.org/10.3389/fcell.2021.727762openalex-snapshot
Ferroptosis Driver SOCS1 and Suppressor FTH1 Independently Correlate With M1 and M2 Macrophage Infiltration in Head and Neck Squamous Cell Carcinoma
inferredcites →https://doi.org/10.3389/fcvm.2021.710963openalex-snapshot
The Link Between Ferroptosis and Cardiovascular Diseases: A Novel Target for Treatment
inferredcites →https://doi.org/10.3389/fimmu.2016.00275openalex-snapshot
M1- and M2-Type Macrophage Responses Are Predictive of Adverse Outcomes in Human Atherosclerosis
inferredcites →https://doi.org/10.3389/fimmu.2019.01347openalex-snapshot
Iron-Dependent Trafficking of 5-Lipoxygenase and Impact on Human Macrophage Activation
inferredcites →https://doi.org/10.3389/fphar.2014.00195openalex-snapshot
The role of iron metabolism as a mediator of macrophage inflammation and lipid handling in atherosclerosis
inferredcites →https://doi.org/10.3389/fphar.2019.00306openalex-snapshot
Macrophage Death as a Pharmacological Target in Atherosclerosis
inferredcites →https://doi.org/10.3389/fphar.2021.673366openalex-snapshot
Traditional Chinese Medication Tongxinluo Attenuates Lipidosis in Ox-LDL-Stimulated Macrophages by Enhancing Beclin-1-Induced Autophagy
inferredcites →https://doi.org/10.3390/antiox8030072openalex-snapshot
Measurement and Clinical Significance of Lipid Peroxidation as a Biomarker of Oxidative Stress: Oxidative Stress in Diabetes, Atherosclerosis, and Chronic Inflammation
inferredcites →https://doi.org/10.3390/nu14020319openalex-snapshot
Decreased Iron Ion Concentrations in the Peripheral Blood Correlate with Coronary Atherosclerosis
inferredcites →https://doi.org/10.3390/ph12010026openalex-snapshot
Curcumin and (−)- Epigallocatechin-3-Gallate Protect Murine MIN6 Pancreatic Beta-Cells against Iron Toxicity and Erastin-Induced Ferroptosis
inferredcites →https://doi.org/10.7150/thno.35528openalex-snapshot
Targeted inhibition of STAT3 as a potential treatment strategy for atherosclerosis
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.4664127openalex-extracted
Iron and Ammonia: A Deadly Combination for Head-Kidney Macrophages of Yellow Catfish (Pelteobagrus Fulvidraco) - Uncovering the Intensified Ferroptosis, Oxidative Stress, and Inflammatory Reactions
inferred← citeshttps://doi.org/10.1002/cbf.70264openalex-snapshot
Cell‐Type–Specific Regulation of Ferroptosis in Atherosclerosis: Mechanisms and Therapeutic Potential of Natural Products
inferred← citeshttps://doi.org/10.1007/s00011-026-02229-2openalex-snapshot
NPC1L1, stabilized by PABPC1/IGF2BP1, accelerates atherosclerosis by enhancing CYP11A1-mediated mitophagy and ferroptosis
inferred← citeshttps://doi.org/10.1007/s00223-026-01477-yopenalex-snapshot
Macrophage Metabolic Reprogramming-Related Osteoimmunity in Osteoporosis
inferred← citeshttps://doi.org/10.1007/s10495-025-02237-3openalex-snapshot
The role and mechanisms of vitamin A in suppressing hepatic stellate cell activation
inferred← citeshttps://doi.org/10.1007/s10735-025-10467-7openalex-snapshot
Porphyromonas gingivalis induced DNA oxidative stress damage by iron overload to deplete CTCF expression and prevent osteogenic differentiation of periodontal ligament stem cells
inferred← citeshttps://doi.org/10.1007/s11010-024-04940-2openalex-snapshot
Molecular mechanisms of ferroptosis in cardiovascular disease
inferred← citeshttps://doi.org/10.1007/s11010-025-05228-9openalex-snapshot
The molecular mechanism by which CTSB degrades FPN to disrupt macrophage iron homeostasis and promote the progression of atherosclerosis
inferred← citeshttps://doi.org/10.1007/s11883-024-01251-1openalex-snapshot
The Role of Iron in Atherosclerosis and its Association with Related Diseases
inferred← citeshttps://doi.org/10.1016/j.abb.2024.109954openalex-snapshot
Iron overload and programmed bone marrow cell death: Potential mechanistic insights
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110316openalex-snapshot
Astaxanthin-loaded polylactic acid-glycolic acid nanoparticles alleviates atherosclerosis by suppressing macrophage ferroptosis via the NRF2/SLC7A11/GPX4 pathway
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110400openalex-snapshot
HSPB1 suppresses oxLDL-induced vascular smooth muscle cell ferroptosis by inhibiting DPP4
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102757openalex-snapshot
Intercellular communication after myocardial infarction: Macrophage as the centerpiece
inferred← citeshttps://doi.org/10.1016/j.bbadis.2026.168240openalex-snapshot
Ferroptosis-driven coronary plaque vulnerability: A tandem mechanism involving endothelial cells, macrophages, and smooth muscle cells
inferred← citeshttps://doi.org/10.1016/j.bbagen.2025.130838openalex-snapshot
EP300-mediated H3K18la regulation of METTL3 promotes macrophage ferroptosis and atherosclerosis through the m6A modification of SLC7A11
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.149788openalex-snapshot
The anti-atherosclerotic effect of Paeonol against the lipid accumulation in macrophage-derived foam cells by inhibiting ferroptosis via the SIRT1/NRF2/GPX4 signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.05.009openalex-snapshot
NIR-responsive bio-system with sequential antibacterial and immunomodulatory effects for the treatment of periodontitis
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117183openalex-snapshot
The complex interplay between ferroptosis and atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117769openalex-snapshot
Ferroptosis in hepatocellular carcinoma: Mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.cellsig.2024.111580openalex-snapshot
New insights into the relationship of mitochondrial metabolism and atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2025.06.007openalex-snapshot
Ferroptosis in immune cells: Implications for tumor immunity and cancer therapy
inferred← citeshttps://doi.org/10.1016/j.dci.2024.105184openalex-snapshot
The differential impact of iron on ferroptosis, oxidative stress, and inflammatory reaction in head-kidney macrophages of yellow catfish (Pelteobagrus fulvidraco) with and without ammonia stress
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.12.046openalex-snapshot
Rab26 alleviates sepsis-induced immunosuppression as a master regulator of macrophage ferroptosis and polarization shift
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.04.025openalex-snapshot
Fut8 regulated Unc5b hyperfucosylation reduces macrophage emigration and accelerates atherosclerosis development via the ferroptosis pathway
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.05.433openalex-snapshot
siHIF-1α-loaded micellar nanoparticles inhibit M1 macrophage activation to ameliorate chronic rhinosinusitis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.06.012openalex-snapshot
Ferro-aging: A novel paradigm linking iron overload, lipid peroxidation and cellular senescence
inferred← citeshttps://doi.org/10.1016/j.gendis.2026.102160openalex-snapshot
Cardiovascular–kidney–metabolic syndrome and targeted therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.gene.2025.149287openalex-snapshot
Identification of novel hub gene and biological pathways associated with ferroptosis in In-Stent restenosis
inferred← citeshttps://doi.org/10.1016/j.gene.2026.150093openalex-snapshot
Based on WGCNA and machine learning studies, SMURF2 drives NSCLC malignant transformation, ferroptosis, and macrophage polarization by ubiquitinating SPP1
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e23507openalex-snapshot
The application of approaches in detecting ferroptosis
inferred← citeshttps://doi.org/10.1016/j.identj.2024.11.018openalex-snapshot
Iron Status and Risk of Periodontitis and Dental Caries: A Mendelian Randomization Study
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113131openalex-snapshot
IFIT2 mediates iron retention and cholesterol efflux in atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113146openalex-snapshot
Targeting ferroptosis in the neurovascular unit: A promising approach for treating diabetic cognitive impairment
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113188openalex-snapshot
The role and mechanism of various trace elements in atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114553openalex-snapshot
Inhibition of ferroptosis alleviates atherosclerosis and foam cell formation by regulating lipid metabolism via AMPK activation
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.116076openalex-snapshot
Vitamin D alleviates diabetic kidney damage via TREM2-dependent modulation of ferritinophagy and macrophage polarization
inferred← citeshttps://doi.org/10.1016/j.isci.2026.115879openalex-snapshot
MicroRNAs as master regulators of macrophage function in atherosclerosis: From polarization to therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.jff.2025.106695openalex-snapshot
Astragaloside IV inhibits atherosclerosis caused by ferritin autophagy in a lipid deposition environment by activating Nrf2
inferred← citeshttps://doi.org/10.1016/j.jtemb.2025.127611openalex-snapshot
Key role of the CSE/transsulfuration pathway in macrophage phenotypic change under iron overload
inferred← citeshttps://doi.org/10.1016/j.neuro.2026.103406openalex-snapshot
The miR-378a-3p/SLC7A11 axis mediates benzo[a]pyrene-induced ferroptosis in hippocampal neuronal cells
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.155489openalex-snapshot
MaiJiTong granule attenuates atherosclerosis by reducing ferroptosis via activating STAT6-mediated inhibition of DMT1 and SOCS1/p53 pathways in LDLR−/− mice
inferred← citeshttps://doi.org/10.1016/j.prp.2024.155353openalex-snapshot
Reflections on the complex mechanisms of endometriosis from the perspective of ferroptosis
inferred← citeshttps://doi.org/10.1016/j.prp.2026.156600openalex-snapshot
Dimethylglycine accelerate atherosclerosis by mediating macrophages ferroptosis via NRF2 pathway suppression
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103465openalex-snapshot
NCOA4 linked to endothelial cell ferritinophagy and ferroptosis:a key regulator aggravate aortic endothelial inflammation and atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.xkme.2026.101324openalex-snapshot
Association of Intravenous Versus Oral Iron Therapy With Clinical Outcomes in Patients With Advanced CKD
inferred← citeshttps://doi.org/10.1016/j.yexcr.2026.115153openalex-snapshot
CTSB promotes ferroptosis in macrophage-derived foam cells and aggravates plaque instability via the NRF2/HMOX1 axis
inferred← citeshttps://doi.org/10.1021/acs.analchem.3c03999openalex-snapshot
Visualization of the Ferroptosis in Atherosclerotic Plaques with Nanoprobe Engineered by Macrophage Cell Membranes
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Quercetin Inhibits Neuronal Pyroptosis and Ferroptosis by Modulating Microglial M1/M2 Polarization in Atherosclerosis
inferred← citeshttps://doi.org/10.1021/cbmi.4c00064openalex-snapshot
Application of Nanomaterials in Early Imaging and Advanced Treatment of Atherosclerosis
inferred← citeshttps://doi.org/10.1038/s41419-025-08357-7openalex-snapshot
Hypoxic tumor exosomes suppress macrophage inflammation and ferroptosis via NDUFV2 to enhance bystander tumor radioresistance
inferred← citeshttps://doi.org/10.1038/s41420-026-03147-2openalex-snapshot
Ferroptosis and macrophage polarization: mechanisms, interplay, and implications for medical applications
inferred← citeshttps://doi.org/10.1038/s42003-024-06756-8openalex-snapshot
Strain heterogeneity in a non-pathogenic Aspergillus fungus highlights factors associated with virulence
inferred← citeshttps://doi.org/10.1039/d5mh01618eopenalex-snapshot
Nanoplatforms synchronously activating tumor cell ferroptosis and remodeling the tumor microenvironment for reinforced cancer therapeutics
inferred← citeshttps://doi.org/10.1063/5.0303714openalex-snapshot
Multi-omics mapping identifies CYBA-mediated mitochondrial dysfunction driving macrophage polarization and ferroptosis via Nrf2 pathway in atherosclerosis
inferred← citeshttps://doi.org/10.1080/03630269.2024.2419889openalex-snapshot
Analysis of Iron Status in Sickle Cell Disease Patients During Steady State at the Center de Recherche et de Lutte contre la Drépanocytose (CRLD) Bamako
inferred← citeshttps://doi.org/10.1093/ckj/sfad190openalex-snapshot
Association of oral iron replacement therapy with kidney failure and mortality in CKD patients
inferred← citeshttps://doi.org/10.1093/cvr/cvae270openalex-snapshot
Iron, lipid peroxidation, and ferroptosis play pathogenic roles in atherosclerosis
inferred← citeshttps://doi.org/10.1093/jimmun/vkag020openalex-snapshot
Cathepsin B promotes asthma potentially via macrophage-associated autophagy and apoptosis
inferred← citeshttps://doi.org/10.1096/fj.202501047rropenalex-snapshot
Paclitaxel Attenuates Atherosclerosis by Suppressing Macrophage Ferroptosis and Improving Lipid Metabolism via the Sirt1/Nrf2/ GPX4 Pathway
inferred← citeshttps://doi.org/10.1101/2024.03.05.583147openalex-snapshot
Changes of urine proteome after intragastric administration of polysaccharide iron complex in rats
inferred← citeshttps://doi.org/10.1101/2024.03.08.583994openalex-snapshot
Strain heterogeneity in a non-pathogenic fungus highlights factors contributing to virulence
inferred← citeshttps://doi.org/10.1101/2024.06.18.599427openalex-snapshot
Pharmacologic Inhibition of Ferroptosis Attenuates Experimental Abdominal Aortic Aneurysm Formation
inferred← citeshttps://doi.org/10.1111/ejh.14091openalex-snapshot
Association of iron therapy with incidence of chronic kidney disease
inferred← citeshttps://doi.org/10.1111/imm.13948openalex-snapshot
Pannexin‐1 Aggravates Inflammatory Bowel Disease via Unbalancing Macrophage Polarisation and Triggering Ferroptosis in Mice
inferred← citeshttps://doi.org/10.1111/jcmm.70729openalex-snapshot
WDFY4 Promotes the Progression of Atherosclerosis by Regulating Ferroptosis Mediated by the LAPTM5 / CDC42 / mTOR / 4EBP1 / SLC7A11 Pathway
inferred← citeshttps://doi.org/10.1161/atvbaha.125.323269openalex-snapshot
Pharmacological Inhibition of Ferroptosis Attenuates Experimental Abdominal Aortic Aneurysm Formation
inferred← citeshttps://doi.org/10.1177/27558428261488938openalex-snapshot
Iron dysregulation in chronic diseases: Mechanistic links between oxidative stress, inflammation, and ferroptosis: A narrative review
inferred← citeshttps://doi.org/10.1186/s12933-024-02224-zopenalex-snapshot
Inhibition of Slc39a14/Slc39a8 reduce vascular calcification via alleviating iron overload induced ferroptosis in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.1186/s13071-024-06144-5openalex-snapshot
Blockage of mechanosensitive Piezo1 channel alleviates the severity of experimental malaria-associated acute lung injury
inferred← citeshttps://doi.org/10.1186/s40001-025-02851-6openalex-snapshot
The interaction between ferroptosis and myocardial ischemia–reperfusion injury: molecular mechanisms and potential therapeutic targets
inferred← citeshttps://doi.org/10.1186/s40164-026-00773-5openalex-snapshot
Decoding the spatiotemporal characteristics of ferroptosis: reshaping tumour therapeutic strategies
inferred← citeshttps://doi.org/10.20517/2394-4722.2026.30openalex-snapshot
Metabolic reprogramming, ferroptosis, and tumor-associated macrophage states: mechanistic crosstalk and therapeutic prospects
inferred← citeshttps://doi.org/10.2147/dddt.s581236openalex-snapshot
The Regulatory Landscape of Ferroptosis and Iron Homeostasis: Pathophysiological Mechanisms and Therapeutic Horizons in Cardiovascular Disease
inferred← citeshttps://doi.org/10.2147/jir.s507076openalex-snapshot
miR-214-3p Promotes ox-LDL-Induced Macrophages Ferroptosis and Inflammation via GPX4
inferred← citeshttps://doi.org/10.2174/0115665240311438241011052341openalex-snapshot
NEDD4 Knockdown Suppresses Human Endometrial Stromal Cell Growth and Invasion by Regulating PTGS2-Mediated Ferroptosis in Endometriosis
inferred← citeshttps://doi.org/10.31083/j.rcm2412358openalex-snapshot
Relation between Systemic Inflammatory Index (SII) and Hair Trace Elements, Metals and Metalloids Concentration in Epicardial Coronary Artery Disease—Preliminary Report
inferred← citeshttps://doi.org/10.31083/j.rcm2510361openalex-snapshot
Iron Overload and Abdominal Aortic Aneurysm
inferred← citeshttps://doi.org/10.31083/j.rcm2512441openalex-snapshot
Ferroptosis: A Key Driver in Atherosclerosis Progression and Arterial Disease
inferred← citeshttps://doi.org/10.31083/rcm45117openalex-snapshot
Ferroptosis of Macrophages and Endothelial Cells in Atherosclerosis: Molecular Mechanisms and Therapeutic Targets
inferred← citeshttps://doi.org/10.3389/fcell.2026.1807359openalex-snapshot
Sesamin attenuates atherosclerosis by alleviating vascular endothelial ferroptosis-related injury via m6A-dependent regulation of SREBF1 expression
inferred← citeshttps://doi.org/10.3389/fcell.2026.1851553openalex-snapshot
Novel insights of ferroptosis in atherosclerosis progression
inferred← citeshttps://doi.org/10.3389/fchem.2025.1543455openalex-snapshot
Major heme proteins hemoglobin and myoglobin with respect to their roles in oxidative stress – a brief review
inferred← citeshttps://doi.org/10.3389/fcvm.2024.1469805openalex-snapshot
Screening of m6A-associated ferroptosis-related genes in atherosclerosis based on WGCNA
inferred← citeshttps://doi.org/10.3389/fendo.2025.1541809openalex-snapshot
The role of metal ion metabolism in the pathogenesis of diabetes and associated complications
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1215612openalex-snapshot
Macrophage death in atherosclerosis: potential role in calcification
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1379967openalex-snapshot
The clinical relevance of heme detoxification by the macrophage heme oxygenase system
inferred← citeshttps://doi.org/10.3389/fimmu.2024.1490387openalex-snapshot
Mechanisms and treatment of atherosclerosis: focus on macrophages
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1628142openalex-snapshot
Immunometabolic crosstalk between tumor- associated macrophages and ferroptotic cancer cells: mechanisms, regulation, and therapeutic applications
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1661805openalex-snapshot
Transient receptor potential channels as key regulators of cell death in atherosclerosis
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1709354openalex-snapshot
Redefining cell death: ferroptosis as a game-changer in ophthalmology
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1831457openalex-snapshot
OxLDL-induced ferroptosis and pyroptosis in atherosclerosis: a mini review
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1868492openalex-snapshot
Ferroptosis in arterial atherosclerosis: mechanistic hypotheses, cell type specific vulnerabilities, translational biomarkers, and therapeutic opportunities
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1889403openalex-snapshot
The role of macrophages in aortic physiology and pathophysiology
inferred← citeshttps://doi.org/10.3389/fphar.2023.1286718openalex-snapshot
The role of ferroptosis in diabetic cardiovascular diseases and the intervention of active ingredients of traditional Chinese medicine
inferred← citeshttps://doi.org/10.3389/fphar.2024.1385565openalex-snapshot
Induction of ferroptosis by natural products in non-small cell lung cancer: a comprehensive systematic review
inferred← citeshttps://doi.org/10.3389/fphar.2025.1516601openalex-snapshot
Ferroptosis, pathogenesis and therapy in AS co-depression disease
inferred← citeshttps://doi.org/10.3389/fphar.2026.1831703openalex-snapshot
Ligusticum chuanxiong and Paeonia lactiflora: a review of their regulation of iron metabolism and ferroptosis in atherosclerosis therapy
inferred← citeshttps://doi.org/10.3389/fphar.2026.1845893openalex-snapshot
The role of tetramethylpyrazine and paeoniflorin in modulating iron metabolism and ferroptosis: innovative strategies for atherosclerosis treatment
inferred← citeshttps://doi.org/10.3389/fphys.2025.1430946openalex-snapshot
Intracellular iron accumulation throughout the progression of sepsis influences the phenotype and function of activated macrophages in renal tissue damage
inferred← citeshttps://doi.org/10.3389/fphys.2026.1905092openalex-snapshot
Homocysteine promotes ferroptosis through NCOA4-mediated ferritinophagy in THP-1 macrophages
inferred← citeshttps://doi.org/10.3390/antiox14010038openalex-snapshot
Deciphering Oxidative Stress in Cardiovascular Disease Progression: A Blueprint for Mechanistic Understanding and Therapeutic Innovation
inferred← citeshttps://doi.org/10.3390/antiox14070890openalex-snapshot
Iron–Immune Crosstalk at the Maternal–Fetal Interface: Emerging Mechanisms in the Pathogenesis of Preeclampsia
inferred← citeshttps://doi.org/10.3390/antiox15030389openalex-snapshot
Reactive Oxygen and Nitrogen Species on Monocyte and Macrophage Biology
inferred← citeshttps://doi.org/10.3390/biom15101464openalex-snapshot
Ferroptosis of Immune Cells in Infection, Inflammation and Tumor Progression
inferred← citeshttps://doi.org/10.3390/ijms241713298openalex-snapshot
Significance of Intra-plaque Hemorrhage for the Development of High-Risk Vulnerable Plaque: Current Understanding from Basic to Clinical Points of View
inferred← citeshttps://doi.org/10.3390/ijms25189758openalex-snapshot
The Protective Role of Interleukin-37 in Cardiovascular Diseases through Ferroptosis Modulation
inferred← citeshttps://doi.org/10.3390/md22110513openalex-snapshot
2-Acetamidophenol (2-AAP) Suppresses the Progression of Atherosclerosis by Alleviating Hyperlipidemia and Attenuating the Ferroptosis Pathway
inferred← citeshttps://doi.org/10.3390/ph18081113openalex-snapshot
Therapeutic Potential of Bioactive Compounds from Traditional Chinese Medicine in Modulating Macrophage Cholesterol Metabolism for Atherosclerosis Treatment.
inferred← citeshttps://doi.org/10.3724/zdxbyxb-2024-0186openalex-snapshot
Research progress on the role of ferroptosis in aortic dissection
inferred← citeshttps://doi.org/10.47316/cajmhe.2025.6.2.02openalex-snapshot
FERROPTOSIS IN MACROPHAGE ACTIVATION SYNDROME AND ADULT-ONSET STILL’S DISEASE
inferred← citeshttps://doi.org/10.6084/m9.figshare.25929188openalex-snapshot
Additional file 1 of Inhibition of Slc39a14/Slc39a8 reduce vascular calcification via alleviating iron overload induced ferroptosis in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.6084/m9.figshare.25929329openalex-snapshot
Additional file 2 of Inhibition of Slc39a14/Slc39a8 reduce vascular calcification via alleviating iron overload induced ferroptosis in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.6084/m9.figshare.26675453openalex-snapshot
Additional file 1 of Blockage of mechanosensitive Piezo1 channel alleviates the severity of experimental malaria-associated acute lung injury
inferred← citeshttps://doi.org/10.6084/m9.figshare.26727304openalex-snapshot
Additional file 3 of Inhibition of Slc39a14/Slc39a8 reduce vascular calcification via alleviating iron overload induced ferroptosis in vascular smooth muscle cells
inferred← citeshttps://doi.org/10.6084/m9.figshare.26727307openalex-snapshot
Additional file 4 of Inhibition of Slc39a14/Slc39a8 reduce vascular calcification via alleviating iron overload induced ferroptosis in vascular smooth muscle cells
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