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Pseudomonas aeruginosa utilizes host polyunsaturated phosphatidylethanolamines to trigger theft-ferroptosis in bronchial epithelium

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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International Study of the Prevalence and Outcomes of Infection in Intensive Care Units

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Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis

inferredcites →https://doi.org/10.1002/14651858.cd004197.pub4openalex-snapshot

Antibiotic strategies for eradicating Pseudomonas aeruginosa in people with cystic fibrosis

inferredcites →https://doi.org/10.1007/82_2011_199openalex-snapshot

Microevolution of Pseudomonas aeruginosa to a Chronic Pathogen of the Cystic Fibrosis Lung

inferredcites →https://doi.org/10.1007/978-1-4615-5325-0_18openalex-snapshot

Mammalian Arachidonate 12-Lipoxygenases

inferredcites →https://doi.org/10.1007/s00018-016-2338-3openalex-snapshot

Ca2+ signals, cell membrane disintegration, and activation of TMEM16F during necroptosis

inferredcites →https://doi.org/10.1007/s00253-013-4887-9openalex-snapshot

Bacterial lipoxygenases, a new subfamily of enzymes? A phylogenetic approach

inferredcites →https://doi.org/10.1016/j.abb.2015.09.003openalex-snapshot

Secreted lipoxygenase from Pseudomonas aeruginosa exhibits biomembrane oxygenase activity and induces hemolysis in human red blood cells

inferredcites →https://doi.org/10.1016/j.bbalip.2009.09.024openalex-snapshot

Acyl-CoA synthesis, lipid metabolism and lipotoxicity

inferredcites →https://doi.org/10.1016/j.bbalip.2013.10.018openalex-snapshot

Differentially localized acyl-CoA synthetase 4 isoenzymes mediate the metabolic channeling of fatty acids towards phosphatidylinositol

inferredcites →https://doi.org/10.1016/j.bbalip.2016.08.002openalex-snapshot

Structural and functional basis of phospholipid oxygenase activity of bacterial lipoxygenase from Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1016/j.bbalip.2017.11.005openalex-snapshot

Specific oxygenation of plasma membrane phospholipids by Pseudomonas aeruginosa lipoxygenase induces structural and functional alterations in mammalian cells

inferredcites →https://doi.org/10.1016/j.cbi.2015.03.011openalex-snapshot

Mechanism for glutathione-mediated protection against the Pseudomonas aeruginosa redox toxin, pyocyanin

inferredcites →https://doi.org/10.1016/j.cell.2013.12.010openalex-snapshot

Regulation of Ferroptotic Cancer Cell Death by GPX4

inferredcites →https://doi.org/10.1016/j.cell.2017.09.044openalex-snapshot

PEBP1 Wardens Ferroptosis by Enabling Lipoxygenase Generation of Lipid Death Signals

inferredcites →https://doi.org/10.1016/j.celrep.2017.02.054openalex-snapshot

Oncogene-Selective Sensitivity to Synchronous Cell Death following Modulation of the Amino Acid Nutrient Cystine

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2014.08.011openalex-snapshot

Nitrite modulates bacterial antibiotic susceptibility and biofilm formation in association with airway epithelial cells

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2017.07.010openalex-snapshot

Glutathione peroxidase 4-catalyzed reduction of lipid hydroperoxides in membranes: The polar head of membrane phospholipids binds the enzyme and addresses the fatty acid hydroperoxide group toward the redox center

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Adaptation of Pseudomonas aeruginosa during persistence in the cystic fibrosis lung

inferredcites →https://doi.org/10.1016/j.jcf.2004.05.040openalex-snapshot

Established cell lines used in cystic fibrosis research

inferredcites →https://doi.org/10.1016/j.plipres.2014.11.001openalex-snapshot

Evolutionary aspects of lipoxygenases and genetic diversity of human leukotriene signaling

inferredcites →https://doi.org/10.1016/j.redox.2016.11.004openalex-snapshot

Inhibition of autophagy with bafilomycin and chloroquine decreases mitochondrial quality and bioenergetic function in primary neurons

inferredcites →https://doi.org/10.1016/j.redox.2017.01.021openalex-snapshot

Ablation of ferroptosis regulator glutathione peroxidase 4 in forebrain neurons promotes cognitive impairment and neurodegeneration

inferredcites →https://doi.org/10.1016/j.tim.2011.04.005openalex-snapshot

Pseudomonas aeruginosa: all roads lead to resistance

inferredcites →https://doi.org/10.1016/s0021-9258(18)64849-5openalex-snapshot

A SIMPLE METHOD FOR THE ISOLATION AND PURIFICATION OF TOTAL LIPIDES FROM ANIMAL TISSUES

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Protective action of phospholipid hydroperoxide glutathione peroxidase against membrane-damaging lipid peroxidation. In situ reduction of phospholipid and cholesterol hydroperoxides.

inferredcites →https://doi.org/10.1016/s0090-6980(02)00035-7openalex-snapshot

Mammalian arachidonate 15-lipoxygenases

inferredcites →https://doi.org/10.1016/s0090-6980(02)00037-0openalex-snapshot

Plant and fungal lipoxygenases

inferredcites →https://doi.org/10.1016/s1286-4579(00)01259-4openalex-snapshot

Establishment of infection: lessons from a versatile opportunist

inferredcites →https://doi.org/10.1021/acs.biochem.6b00338openalex-snapshot

Biochemical and Cellular Characterization and Inhibitor Discovery of Pseudomonas aeruginosa 15-Lipoxygenase

inferredcites →https://doi.org/10.1021/acs.jmedchem.5b01641openalex-snapshot

Novel Ferroptosis Inhibitors with Improved Potency and ADME Properties

inferredcites →https://doi.org/10.1021/ci300604zopenalex-snapshot

Lessons Learned in Empirical Scoring with smina from the CSAR 2011 Benchmarking Exercise

inferredcites →https://doi.org/10.1021/cr200246dopenalex-snapshot

Lipoxygenase and Leukotriene Pathways: Biochemistry, Biology, and Roles in Disease

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/nchembio.2238openalex-snapshot

Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis

inferredcites →https://doi.org/10.1038/ng.3148openalex-snapshot

Convergent evolution and adaptation of Pseudomonas aeruginosa within patients with cystic fibrosis

inferredcites →https://doi.org/10.1038/nnano.2016.164openalex-snapshot

Ultrasmall nanoparticles induce ferroptosis in nutrient-deprived cancer cells and suppress tumour growth

inferredcites →https://doi.org/10.1038/nprot.2006.24openalex-snapshot

mini-Tn7 insertion in bacteria with single attTn7 sites: example Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1038/nrmicro2907openalex-snapshot

Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective

inferredcites →https://doi.org/10.1038/nsb1297-1003openalex-snapshot

The structure of mammalian 15-lipoxygenase reveals similarity to the lipases and the determinants of substrate specificity

inferredcites →https://doi.org/10.1038/s41589-018-0031-6openalex-snapshot

FINO2 initiates ferroptosis through GPX4 inactivation and iron oxidation

inferredcites →https://doi.org/10.1039/c2ra20816dopenalex-snapshot

A novel fluorescent probe with high sensitivity and selective detection of lipid hydroperoxides in cells

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00797.xopenalex-snapshot

Initiation of biofilm formation in Pseudomonas fluorescens WCS365 proceeds via multiple, convergent signalling pathways: a genetic analysis

inferredcites →https://doi.org/10.1073/pnas.0307308101openalex-snapshot

The opportunistic pathogen Pseudomonas aeruginosa carries a secretable arachidonate 15-lipoxygenase

inferredcites →https://doi.org/10.1073/pnas.0602138103openalex-snapshot

Genetic adaptation by Pseudomonas aeruginosa to the airways of cystic fibrosis patients

inferredcites →https://doi.org/10.1073/pnas.0602526103openalex-snapshot

Evolving stealth: Genetic adaptation of Pseudomonas aeruginosa during cystic fibrosis infections

inferredcites →https://doi.org/10.1073/pnas.1207025110openalex-snapshot

Tangled bank of experimentally evolved Burkholderia biofilms reflects selection during chronic infections

inferredcites →https://doi.org/10.1073/pnas.1415518111openalex-snapshot

Synchronized renal tubular cell death involves ferroptosis

inferredcites →https://doi.org/10.1073/pnas.1603244113openalex-snapshot

Peroxidation of polyunsaturated fatty acids by lipoxygenases drives ferroptosis

inferredcites →https://doi.org/10.1073/pnas.1607152113openalex-snapshot

Activation of SAT1 engages polyamine metabolism with p53-mediated ferroptotic responses

inferredcites →https://doi.org/10.1073/pnas.1610242114openalex-snapshot

Pseudomonas aeruginosa sabotages the generation of host proresolving lipid mediators

inferredcites →https://doi.org/10.1073/pnas.2036282100openalex-snapshot

Comprehensive transposon mutant library of Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1074/jbc.m113.543777openalex-snapshot

The Structure of Human 15-Lipoxygenase-2 with a Substrate Mimic

inferredcites →https://doi.org/10.1083/jcb.201605110openalex-snapshot

Heat stress induces ferroptosis-like cell death in plants

inferredcites →https://doi.org/10.1093/bioinformatics/bts091openalex-snapshot

Unipro UGENE: a unified bioinformatics toolkit

inferredcites →https://doi.org/10.1093/bioinformatics/btu336openalex-snapshot

Evol and ProDy for bridging protein sequence evolution and structural dynamics

inferredcites →https://doi.org/10.1093/bioinformatics/btu847openalex-snapshot

The anisotropic network model web server at 2015 (ANM 2.0)

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/nar/gkv1236openalex-snapshot

iGNM 2.0: the Gaussian network model database for biomolecular structural dynamics

inferredcites →https://doi.org/10.1093/nar/gkv1344openalex-snapshot

The Pfam protein families database: towards a more sustainable future

inferredcites →https://doi.org/10.1093/nar/gkx385openalex-snapshot

DynOmics: dynamics of structural proteome and beyond

inferredcites →https://doi.org/10.1096/fj.13-235952openalex-snapshot

Structure and interaction with phospholipids of a prokaryotic lipoxygenase from Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1097/01.ccm.0000194725.48928.3aopenalex-snapshot

Sepsis in European intensive care units: Results of the SOAP study*

inferredcites →https://doi.org/10.1099/00222615-45-2-110openalex-snapshot

The high amino-acid content of sputum from cystic fibrosis patients promotes growth of auxotrophic Pseudomonas aeruginosa

inferredcites →https://doi.org/10.1099/13500872-145-4-767openalex-snapshot

Polyunsaturated fatty acids in marine bacteria — a dogma rewritten

inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02253.xopenalex-snapshot

How Pseudomonas aeruginosa adapts to various environments: a metabolomic approach

inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00269.xopenalex-snapshot

Pseudomonas genomes: diverse and adaptable

inferredcites →https://doi.org/10.1111/j.2517-6161.1964.tb00553.xopenalex-snapshot

An Analysis of Transformations

inferredcites →https://doi.org/10.1126/science.288.5469.1251openalex-snapshot

High Frequency of Hypermutable Pseudomonas aeruginosa in Cystic Fibrosis Lung Infection

inferredcites →https://doi.org/10.1128/jb.00119-09openalex-snapshot

Pseudomonas aeruginosa Rugose Small-Colony Variants Have Adaptations That Likely Promote Persistence in the Cystic Fibrosis Lung

inferredcites →https://doi.org/10.1128/jb.01760-14openalex-snapshot

Epoxide-Mediated Differential Packaging of Cif and Other Virulence Factors into Outer Membrane Vesicles

inferredcites →https://doi.org/10.1128/mmbr.60.3.539-574.1996openalex-snapshot

Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia

inferredcites →https://doi.org/10.1164/rccm.200812-1943ocopenalex-snapshot

Pseudomonas aeruginosa Microevolution during Cystic Fibrosis Lung Infection Establishes Clones with Adapted Virulence

inferredcites →https://doi.org/10.1186/1471-2105-5-113openalex-snapshot

MUSCLE: a multiple sequence alignment method with reduced time and space complexity

inferredcites →https://doi.org/10.1371/journal.ppat.1000382openalex-snapshot

Long-Distance Delivery of Bacterial Virulence Factors by Pseudomonas aeruginosa Outer Membrane Vesicles

inferredcites →https://doi.org/10.3389/fcimb.2017.00039openalex-snapshot

Pseudomonas aeruginosa Lifestyle: A Paradigm for Adaptation, Survival, and Persistence

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Ferroptosis and iron mineralization involved in the death and survival of orange‐spotted groupers challenged with Pseudomonas plecoglossicida

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Crosstalk Between Microbiome and Ferroptosis in Diseases: From Mechanism to Therapy

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Ferroptosis in Cancer and Inflammatory Diseases: Mechanisms and Therapeutic Implications

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Changes in ferroptosis-related molecular expression in macrophages of community-acquired pneumonia patients and their associated with the disease progression

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inferred← citeshttps://doi.org/10.1016/j.isci.2023.107700openalex-snapshot

Spatial lipidomics reveals biased phospholipid remodeling in acute Pseudomonas lung infection

inferred← citeshttps://doi.org/10.1016/j.jare.2023.09.042openalex-snapshot

IFP35 aggravates Staphylococcus aureus infection by promoting Nrf2-regulated ferroptosis

inferred← citeshttps://doi.org/10.1016/j.jdsr.2025.08.001openalex-snapshot

Interplay between survival and regulated cell death mechanisms during periodontitis progression: a systematic review

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.137969openalex-snapshot

Isobavachalcone confers protection against Cryptococcus neoformans-induced ferroptosis in Caenorhabditis elegans via lifespan extension and GSH-GPX-1 axis modulation

inferred← citeshttps://doi.org/10.1016/j.jid.2025.06.1289openalex-snapshot

Emerging Roles of Ferroptosis in Skin Pathophysiology

inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169009openalex-snapshot

InSty: A ProDy Module for Evaluating Protein Interactions and Stability

inferred← citeshttps://doi.org/10.1016/j.jpha.2024.101050openalex-snapshot

The molecular and metabolic landscape of ferroptosis in respiratory diseases: Pharmacological aspects

inferred← citeshttps://doi.org/10.1016/j.jpha.2026.101551openalex-snapshot

Nano-formulations in therapeutic strategies targeting cancer ferroptosis

inferred← citeshttps://doi.org/10.1016/j.matdes.2026.115505openalex-snapshot

Hollow cerium oxide nanoparticles promote M2 polarization and modulate the SLC7A11/GSH/GPX4 axis to attenuate macrophage ferroptosis for inflammatory wound repair

inferred← citeshttps://doi.org/10.1016/j.matdes.2026.116713openalex-snapshot

Dual-function niobium-doped carbon dots for ferroptosis-driven anti-inflammatory therapy in pseudomonas aeruginosa pneumonia via GPX4 axis

inferred← citeshttps://doi.org/10.1016/j.micres.2024.127728openalex-snapshot

Induction of ferroptosis: A new strategy for the control of bacterial infections

inferred← citeshttps://doi.org/10.1016/j.mito.2020.06.008openalex-snapshot

Mitochondria and microbiota dysfunction in COVID-19 pathogenesis

inferred← citeshttps://doi.org/10.1016/j.nantod.2023.101865openalex-snapshot

The role of mesenchymal stem cell-derived extracellular vesicles in inflammation-associated programmed cell death

inferred← citeshttps://doi.org/10.1016/j.nefro.2020.03.005openalex-snapshot

Ferroptosis and kidney disease

inferred← citeshttps://doi.org/10.1016/j.nefroe.2020.09.006openalex-snapshot

Ferroptosis and kidney disease

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2020.04.001openalex-snapshot

Ferroptosis as an emerging target in inflammatory diseases

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.107992openalex-snapshot

Emerging role of ferroptosis in breast cancer: New dawn for overcoming tumor progression

inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105305openalex-snapshot

Flubendazole, FDA-approved anthelmintic, elicits valid antitumor effects by targeting P53 and promoting ferroptosis in castration-resistant prostate cancer

inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107223openalex-snapshot

The emerging role of adaptor proteins in regulating innate immunity of sepsis

inferred← citeshttps://doi.org/10.1016/j.phymed.2024.156189openalex-snapshot

Yi-Qi-Jian-Pi-Xiao-Yu formula inhibits cisplatin-induced acute kidney injury through suppressing ferroptosis via STING-NCOA4-mediated ferritinophagy

inferred← citeshttps://doi.org/10.1016/j.redox.2020.101744openalex-snapshot

Resolving the paradox of ferroptotic cell death: Ferrostatin-1 binds to 15LOX/PEBP1 complex, suppresses generation of peroxidized ETE-PE, and protects against ferroptosis

inferred← citeshttps://doi.org/10.1016/j.redox.2021.102045openalex-snapshot

A new thiol-independent mechanism of epithelial host defense against Pseudomonas aeruginosa: iNOS/NO• sabotage of theft-ferroptosis

inferred← citeshttps://doi.org/10.1016/j.redox.2022.102467openalex-snapshot

NLRP3 inflammasome activation in cigarette smoke priming for Pseudomonas aeruginosa-induced acute lung injury

inferred← citeshttps://doi.org/10.1016/j.redox.2023.102650openalex-snapshot

Redox phospholipidomics discovers pro-ferroptotic death signals in A375 melanoma cells in vitro and in vivo

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.177534openalex-snapshot

A comprehensive review of ferroptosis in environmental pollutants-induced chronic obstructive pulmonary disease

inferred← citeshttps://doi.org/10.1016/j.semcancer.2019.03.002openalex-snapshot

Ferroptosis is a type of autophagy-dependent cell death

inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.12.005openalex-snapshot

Iron in immune cell function and host defense

inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.11.061openalex-snapshot

Therapeutic potential of induced iron depletion using iron chelators in Covid-19

inferred← citeshttps://doi.org/10.1016/j.taap.2025.117590openalex-snapshot

PM2.5 enhances DRP1-mediated mitochondrial fission to induce ferroptosis and exacerbate asthma through the AHR-HSP90-PKM2 pathway

inferred← citeshttps://doi.org/10.1016/j.tim.2022.11.006openalex-snapshot

When ferroptosis meets pathogenic infections

inferred← citeshttps://doi.org/10.1016/j.vetmic.2025.110538openalex-snapshot

Autophagy is involved in Salmonella Typhimurium-induced ferroptosis in macrophages

inferred← citeshttps://doi.org/10.1016/j.xcrm.2026.103003openalex-snapshot

Spatiotemporal iron-hijacking hydrogel reprograms host-pathogen iron homeostasis for fungal keratitis therapy

inferred← citeshttps://doi.org/10.1016/j.yexcr.2023.113612openalex-snapshot

Ebselen restores peri-implantitis-induced osteogenic inhibition via suppressing BMSCs ferroptosis

inferred← citeshttps://doi.org/10.1016/j.yexcr.2024.114039openalex-snapshot

STING mediates LPS-induced acute lung injury by regulating ferroptosis

inferred← citeshttps://doi.org/10.1021/acs.jcim.9b00006openalex-snapshot

Characterization of Differential Dynamics, Specificity, and Allostery of Lipoxygenase Family Members

inferred← citeshttps://doi.org/10.1038/s12276-023-01069-yopenalex-snapshot

Regulated cell death pathways and their roles in homeostasis, infection, inflammation, and tumorigenesis

inferred← citeshttps://doi.org/10.1038/s41368-024-00306-yopenalex-snapshot

A multi-platform analysis of human gingival crevicular fluid reveals ferroptosis as a relevant regulated cell death mechanism during the clinical progression of periodontitis

inferred← citeshttps://doi.org/10.1038/s41392-020-00428-9openalex-snapshot

Ferroptosis: mechanisms and links with diseases

inferred← citeshttps://doi.org/10.1038/s41392-023-01606-1openalex-snapshot

Targeting ferroptosis opens new avenues for the development of novel therapeutics

inferred← citeshttps://doi.org/10.1038/s41418-022-00998-xopenalex-snapshot

Non-coding RNAs and ferroptosis: potential implications for cancer therapy

inferred← citeshttps://doi.org/10.1038/s41418-022-01060-6openalex-snapshot

Dying in self-defence: a comparative overview of immunogenic cell death signalling in animals and plants

inferred← citeshttps://doi.org/10.1038/s41419-022-05070-7openalex-snapshot

Targeting ferroptosis as a vulnerability in pulmonary diseases

inferred← citeshttps://doi.org/10.1038/s41419-024-06467-2openalex-snapshot

HMGA1 drives chemoresistance in esophageal squamous cell carcinoma by suppressing ferroptosis

inferred← citeshttps://doi.org/10.1038/s41419-025-07800-zopenalex-snapshot

Stress granules and cell death: crosstalk and potential therapeutic strategies in infectious diseases

inferred← citeshttps://doi.org/10.1038/s41419-026-09071-8openalex-snapshot

Lipid peroxidation impacts orthoflavivirus infection in a virus-dependent manner

inferred← citeshttps://doi.org/10.1038/s41420-022-01212-0openalex-snapshot

GPX4-independent ferroptosis—a new strategy in disease’s therapy

inferred← citeshttps://doi.org/10.1038/s41420-023-01482-2openalex-snapshot

Ferrostatin-1 alleviates the damage of C2C12 myoblast and mouse pelvic floor muscle induced by mechanical trauma

inferred← citeshttps://doi.org/10.1038/s41420-024-02189-8openalex-snapshot

Unveiling the crucial role of ferroptosis in host resistance to streptococcus agalactiae infection

inferred← citeshttps://doi.org/10.1038/s41420-025-02550-5openalex-snapshot

Ferroptosis in periodontitis: mechanisms, impacts, and systemic connections

inferred← citeshttps://doi.org/10.1038/s41420-026-03067-1openalex-snapshot

Targeting the ODC1-YBX1 axis reverses gastric cancer chemoresistance via transcriptional control of SLC7A11-mediated ferroptosis

inferred← citeshttps://doi.org/10.1038/s41422-020-00441-1openalex-snapshot

Ferroptosis: molecular mechanisms and health implications

inferred← citeshttps://doi.org/10.1038/s41467-021-24469-yopenalex-snapshot

Prokineticin-2 prevents neuronal cell deaths in a model of traumatic brain injury

inferred← citeshttps://doi.org/10.1038/s41467-022-33735-6openalex-snapshot

TLCD1 and TLCD2 regulate cellular phosphatidylethanolamine composition and promote the progression of non-alcoholic steatohepatitis

inferred← citeshttps://doi.org/10.1038/s41467-023-37148-xopenalex-snapshot

A mycobacterial effector promotes ferroptosis-dependent pathogenicity and dissemination

inferred← citeshttps://doi.org/10.1038/s41467-023-37149-wopenalex-snapshot

Ferroptosis hijacking by Mycobacterium tuberculosis

inferred← citeshttps://doi.org/10.1038/s41467-025-65142-yopenalex-snapshot

A Pseudomonas aeruginosa quorum-sensing metabolite manipulates macrophage ferroptosis through a methylation pathway

inferred← citeshttps://doi.org/10.1038/s41564-021-00961-5openalex-snapshot

Microbial signatures in the lower airways of mechanically ventilated COVID-19 patients associated with poor clinical outcome

inferred← citeshttps://doi.org/10.1038/s41568-019-0149-1openalex-snapshot

Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion

inferred← citeshttps://doi.org/10.1038/s41580-020-00324-8openalex-snapshot

Ferroptosis: mechanisms, biology and role in disease

inferred← citeshttps://doi.org/10.1038/s41580-024-00703-5openalex-snapshot

The cell biology of ferroptosis

inferred← citeshttps://doi.org/10.1038/s41581-023-00689-xopenalex-snapshot

Ferroptotic mechanisms and therapeutic targeting of iron metabolism and lipid peroxidation in the kidney

inferred← citeshttps://doi.org/10.1038/s41589-019-0408-1openalex-snapshot

The chemical basis of ferroptosis

inferred← citeshttps://doi.org/10.1038/s41589-019-0462-8openalex-snapshot

Redox lipid reprogramming commands susceptibility of macrophages and microglia to ferroptotic death

inferred← citeshttps://doi.org/10.1038/s41598-025-29557-3openalex-snapshot

Ferroptosis mediated by ferritinophagy is involved in liver injury caused by sepsis

inferred← citeshttps://doi.org/10.1073/pnas.2218896120openalex-snapshot

Discovering selective antiferroptotic inhibitors of the 15LOX/PEBP1 complex noninterfering with biosynthesis of lipid mediators

inferred← citeshttps://doi.org/10.1080/01652176.2025.2569558openalex-snapshot

Ferroptosis in veterinary medicine: mechanisms, therapies, and unmet challenges

inferred← citeshttps://doi.org/10.1080/15548627.2025.2468139openalex-snapshot

Mycobacterium bovis Mb3523c protein regulates host ferroptosis via chaperone-mediated autophagy

inferred← citeshttps://doi.org/10.1080/19490976.2023.2263210openalex-snapshot

The influence of microbiota on ferroptosis in intestinal diseases

inferred← citeshttps://doi.org/10.1080/20002297.2024.2334578openalex-snapshot

Role of ferroptosis in Porphyromonas gingivalis- induced impairment of epithelial junction

inferred← citeshttps://doi.org/10.1080/21505594.2025.2530164openalex-snapshot

Ferroptosis is important for Toxoplasma gondii replication and virulence in vitro and in vivo

inferred← citeshttps://doi.org/10.1080/21505594.2025.2553787openalex-snapshot

Ferroptosis and iron-based therapies in Pseudomonas aeruginosa infections: From pathogenesis to treatment

inferred← citeshttps://doi.org/10.1083/jcb.201911005openalex-snapshot

C-ferroptosis is an iron-dependent form of regulated cell death in cyanobacteria

inferred← citeshttps://doi.org/10.1084/jem.20190038openalex-snapshot

Die another way: Ferroptosis drives tuberculosis pathology

inferred← citeshttps://doi.org/10.1084/jem.20210518openalex-snapshot

Ferroptosis in infection, inflammation, and immunity

inferred← citeshttps://doi.org/10.1089/ars.2020.8175openalex-snapshot

Ferroptosis: Biological Rust of Lipid Membranes

inferred← citeshttps://doi.org/10.1089/ars.2021.0079openalex-snapshot

Redox Pioneer: Professor Valerian Kagan

inferred← citeshttps://doi.org/10.1089/ars.2022.0169openalex-snapshot

Dapagliflozin Alleviates Diabetic Kidney Disease via Hypoxia Inducible Factor 1α/Heme Oxygenase 1-Mediated Ferroptosis

inferred← citeshttps://doi.org/10.1089/ars.2022.0209openalex-snapshot

Mitochondrial Reactive Oxygen Species and Lytic Programmed Cell Death in Acute Inflammation

inferred← citeshttps://doi.org/10.1093/nar/gkaa377openalex-snapshot

PvrA is a novel regulator that contributes to Pseudomonas aeruginosa pathogenesis by controlling bacterial utilization of long chain fatty acids

inferred← citeshttps://doi.org/10.1097/sla.0000000000005252openalex-snapshot

Pseudomonas Aeruginosa Theft Biofilm Require Host Lipids of Cutaneous Wound

inferred← citeshttps://doi.org/10.1101/2022.06.21.497025openalex-snapshot

Bacterial lipoxygenases are associated with host-microbe interactions and may provide cross-kingdom host jumps

inferred← citeshttps://doi.org/10.1101/2022.10.24.513460openalex-snapshot

A Compensatory RNase E Variation Increases Iron Piracy and Virulence in Multidrug-Resistant Pseudomonas aeruginosa during Macrophage Infection

inferred← citeshttps://doi.org/10.1101/2023.01.23.524390openalex-snapshot

Lack of Fzd6 in Ciliated Cells Suppresses Ferroptotic Pulmonary Alveolar Cell Death Induced by LPS and Coronavirus

inferred← citeshttps://doi.org/10.1101/2023.12.20.572489openalex-snapshot

Chlamydial protease-like activating factor targets SLC7A11 for degradation to induce ferroptosis and facilitate dissemination

inferred← citeshttps://doi.org/10.1111/febs.16244openalex-snapshot

Emerging roles of ferroptosis in infectious diseases

inferred← citeshttps://doi.org/10.1111/febs.16981openalex-snapshot

A guide to the expanding field of extracellular vesicles and their release in regulated cell death programs

inferred← citeshttps://doi.org/10.1111/imr.12892openalex-snapshot

Cross talk between intracellular pathogens and cell death

inferred← citeshttps://doi.org/10.1111/imr.13235openalex-snapshot

Ferroptosis in immunostimulation and immunosuppression

inferred← citeshttps://doi.org/10.1111/raq.12719openalex-snapshot

The role of ferroptosis in fish inflammation

inferred← citeshttps://doi.org/10.1126/sciadv.aeb5297openalex-snapshot

Enterococcus faecalis redox metabolism activates the unfolded protein response to impair wound healing

inferred← citeshttps://doi.org/10.1128/spectrum.03837-25openalex-snapshot

Sinomenine protects mice against Staphylococcus aureus -induced endometritis through inhibition of P2X7 receptor-mediated ferroptosis and inflammation

inferred← citeshttps://doi.org/10.1128/spectrum.03923-25openalex-snapshot

Mediating ferritinophagy and ferroptosis: a novel strategy against Staphylococcus aureus infection from a Kudzu root endophytic fungus

inferred← citeshttps://doi.org/10.1134/s0006297920090059openalex-snapshot

Bacterial and Protozoan Lipoxygenases Could be Involved in Cell-to-Cell Signaling and Immune Response Suppression

inferred← citeshttps://doi.org/10.1146/annurev-nutr-062320-114541openalex-snapshot

Nutritional and Metabolic Control of Ferroptosis

inferred← citeshttps://doi.org/10.1152/ajplung.00065.2019openalex-snapshot

Collateral damage: necroptosis in the development of lung injury

inferred← citeshttps://doi.org/10.1152/physrev.00031.2024openalex-snapshot

Ferroptosis: when metabolism meets cell death

inferred← citeshttps://doi.org/10.1155/2020/9547127openalex-snapshot

Molecular Mechanisms of Ferroptosis and Its Role in Pulmonary Disease

inferred← citeshttps://doi.org/10.1155/2021/1098970openalex-snapshot

Targeting Ferroptosis for Lung Diseases: Exploring Novel Strategies in Ferroptosis‐Associated Mechanisms

inferred← citeshttps://doi.org/10.1155/2022/5295434openalex-snapshot

Physiological Effects of Ferroptosis on Organ Fibrosis

inferred← citeshttps://doi.org/10.1155/2023/3875897openalex-snapshot

Ferroptosis Is a Potential Therapeutic Target for Pulmonary Infectious Diseases

inferred← citeshttps://doi.org/10.1165/rcmb.2019-0337tropenalex-snapshot

Regulated Necrosis in Pulmonary Disease. A Focus on Necroptosis and Ferroptosis

inferred← citeshttps://doi.org/10.1167/iovs.65.2.29openalex-snapshot

Ferroptosis as a Potential Therapeutic Target for Reducing Inflammation and Corneal Scarring in Bacterial Keratitis

inferred← citeshttps://doi.org/10.1172/jci.insight.156013openalex-snapshot

P. aeruginosa augments irradiation injury via 15-lipoxygenase–catalyzed generation of 15-HpETE-PE and induction of theft-ferroptosis

inferred← citeshttps://doi.org/10.1172/jci183219openalex-snapshot

Ferroptosis of select skin epithelial cells initiates and maintains chronic systemic immune-mediated psoriatic disease

inferred← citeshttps://doi.org/10.1177/00368504221147173openalex-snapshot

Targeting critical pathways in ferroptosis and enhancing antitumor therapy of Platinum drugs for colorectal cancer

inferred← citeshttps://doi.org/10.1177/17534666231208628openalex-snapshot

Ferroptosis triggers airway inflammation in asthma

inferred← citeshttps://doi.org/10.1186/s12951-025-03457-0openalex-snapshot

Outer membrane vesicles of Porphyromonas gingivalis impede bone regeneration by inducing ferroptosis via the Hippo-YAP signaling pathway

inferred← citeshttps://doi.org/10.1186/s13054-025-05278-xopenalex-snapshot

The role of programmed cell death in organ dysfunction induced by opportunistic pathogens

inferred← citeshttps://doi.org/10.1186/s13071-025-07207-xopenalex-snapshot

Toxoplasma gondii-induced ferroptosis contributes to acute lung injury in mice

inferred← citeshttps://doi.org/10.1186/s43556-026-00420-9openalex-snapshot

Ferroptosis in cardiovascular diseases: molecular mechanisms and a novel therapeutic target

inferred← citeshttps://doi.org/10.12677/acm.2025.151178openalex-snapshot

Research Progress on Iron Overload and Lung Diseases

inferred← citeshttps://doi.org/10.1371/journal.ppat.1009927openalex-snapshot

Host phospholipid peroxidation fuels ExoU-dependent cell necrosis and supports Pseudomonas aeruginosa-driven pathology

inferred← citeshttps://doi.org/10.1371/journal.ppat.1010942openalex-snapshot

A compensatory RNase E variation increases Iron Piracy and Virulence in multidrug-resistant Pseudomonas aeruginosa during Macrophage infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1013060openalex-snapshot

Chlamydial protease-like activity factor targets SLC7A11 for degradation to induce ferroptosis and facilitate progeny releases

inferred← citeshttps://doi.org/10.1667/rr15379.1openalex-snapshot

Radioresistance of Serpinb3a−/− Mice and Derived Hematopoietic and Marrow Stromal Cell Lines

inferred← citeshttps://doi.org/10.1667/rr15486.1openalex-snapshot

Anti-Ferroptosis Drug Enhances Total-Body Irradiation Mitigation by Drugs that Block Apoptosis and Necroptosis

inferred← citeshttps://doi.org/10.20455/ros.2019.835openalex-snapshot

GPx4 in Bacterial Infection and Polymicrobial Sepsis: Involvement of Ferroptosis and Pyroptosis

inferred← citeshttps://doi.org/10.21203/rs.3.rs-1745222/v1openalex-snapshot

Dapagliflozin alleviates diabetic kidney disease via HIF‐1α/HO1 mediated ferroptosis

inferred← citeshttps://doi.org/10.21248/gups.85835openalex-snapshot

Synthesis and biological characterization of esterified lipid mediators

inferred← citeshttps://doi.org/10.2147/idr.s528964openalex-snapshot

Hydroxysafflor Yellow A Mitigates Sepsis-Induced Pulmonary and Intestinal Injury by Inhibiting TP53 Mediated Ferroptosis

inferred← citeshttps://doi.org/10.2147/ijn.s586869openalex-snapshot

Ferroptosis-Like Death: An Emerging Innovative Antibacterial Strategy

inferred← citeshttps://doi.org/10.2147/jir.s307081openalex-snapshot

Role of Ferroptosis in Lung Diseases

inferred← citeshttps://doi.org/10.2147/jir.s457092openalex-snapshot

Unraveling the Molecular Regulation of Ferroptosis in Respiratory Diseases

inferred← citeshttps://doi.org/10.2147/jir.s571504openalex-snapshot

Circulating and Respiratory Biomarkers in Sepsis-Induced ARDS: Diagnostic and Prognostic Insights – A Narrative Review

inferred← citeshttps://doi.org/10.2147/jmdh.s382643openalex-snapshot

The Relationship Between Ferroptosis and Diseases

inferred← citeshttps://doi.org/10.21873/invivo.11742openalex-snapshot

Fanconi Anemia Mouse Genotype-specific Mitigation of Total Body Irradiation by GS-Nitroxide JP4-039

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