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Radiation-Induced Lipid Peroxidation Triggers Ferroptosis and Synergizes with Ferroptosis Inducers
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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The role of radiotherapy in cancer treatment
inferredcites →https://doi.org/10.1007/978-1-4684-5457-4openalex-snapshot
Prostaglandin and Lipid Metabolism in Radiation Injury
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Methods for Studying TNF-Mediated Necroptosis in Cultured Cells
inferredcites →https://doi.org/10.1007/s11745-997-0035-yopenalex-snapshot
Polyunsaturated fatty acids increase the sensitivity of 36B10 rat astrocytoma cells to radiation‐induced cell kill
inferredcites →https://doi.org/10.1007/s13277-010-0042-8openalex-snapshot
Radiation-induced cell death mechanisms
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.2013.09.034openalex-snapshot
The Somatic Genomic Landscape of Glioblastoma
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.2014.04.004openalex-snapshot
The Somatic Genomic Landscape of Glioblastoma
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.chembiol.2019.01.008openalex-snapshot
Imidazole Ketone Erastin Induces Ferroptosis and Slows Tumor Growth in a Mouse Lymphoma Model
inferredcites →https://doi.org/10.1016/j.clnu.2013.04.005openalex-snapshot
Interaction of ω-3 polyunsaturated fatty acids with radiation therapy in two different colorectal cancer cell lines
inferredcites →https://doi.org/10.1016/j.clon.2013.06.007openalex-snapshot
Biological Consequences of Radiation-induced DNA Damage: Relevance to Radiotherapy
inferredcites →https://doi.org/10.1016/j.ijrobp.2017.05.016openalex-snapshot
Quality Assessment of Stereotactic Radiosurgery of a Melanoma Brain Metastases Model Using a Mouselike Phantom and the Small Animal Radiation Research Platform
inferredcites →https://doi.org/10.1016/j.nima.2009.08.041openalex-snapshot
The Columbia University sub-micron charged particle beam
inferredcites →https://doi.org/10.1016/j.surg.2011.09.012openalex-snapshot
Necroptosis is a novel mechanism of radiation-induced cell death in anaplastic thyroid and adrenocortical cancers
inferredcites →https://doi.org/10.1016/j.tcb.2015.10.014openalex-snapshot
Ferroptosis: Death by Lipid Peroxidation
inferredcites →https://doi.org/10.1016/s0022-2275(20)33425-8openalex-snapshot
Lysophosphatidylcholine-induced cellular injury in cultured fibroblasts involves oxidative events
inferredcites →https://doi.org/10.1038/cr.2016.95openalex-snapshot
Ferroptosis is an autophagic cell death process
inferredcites →https://doi.org/10.1038/nature05859openalex-snapshot
RAS–RAF–MEK-dependent oxidative cell death involving voltage-dependent anion channels
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Dependency of a therapy-resistant state of cancer cells on a lipid peroxidase pathway
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inferredcites →https://doi.org/10.1038/s41418-019-0393-7openalex-snapshot
Kinome screen of ferroptosis reveals a novel role of ATM in regulating iron metabolism
inferredcites →https://doi.org/10.1038/s41467-019-09277-9openalex-snapshot
A GPX4-dependent cancer cell state underlies the clear-cell morphology and confers sensitivity to ferroptosis
inferredcites →https://doi.org/10.1038/s41589-018-0031-6openalex-snapshot
FINO2 initiates ferroptosis through GPX4 inactivation and iron oxidation
inferredcites →https://doi.org/10.1056/nejmoa1402121openalex-snapshot
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas
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.94.8.3765openalex-snapshot
Mutagenic effects of a single and an exact number of α particles in mammalian cells
inferredcites →https://doi.org/10.1073/pnas.96.9.4959openalex-snapshot
Targeted cytoplasmic irradiation with alpha particles induces mutations in mammalian cells
inferredcites →https://doi.org/10.1080/09553000110104065openalex-snapshot
Radiation-induced peroxidation and fragmentation of lipids in a model membrane
inferredcites →https://doi.org/10.1080/09553007914550391openalex-snapshot
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inferredcites →https://doi.org/10.1146/annurev-med-081313-121208openalex-snapshot
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inferredcites →https://doi.org/10.1158/1078-0432.ccr-13-3229openalex-snapshot
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inferredcites →https://doi.org/10.1158/1078-0432.ccr-15-2869openalex-snapshot
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inferredcites →https://doi.org/10.1158/2159-8290.cd-19-0338openalex-snapshot
Radiotherapy and Immunotherapy Promote Tumoral Lipid Oxidation and Ferroptosis via Synergistic Repression of SLC7A11
inferredcites →https://doi.org/10.1269/jrr.08120sopenalex-snapshot
Consequences of Cytoplasmic Irradiation: Studies from Microbeam
inferredcites →https://doi.org/10.1371/journal.pone.0195151openalex-snapshot
Sulfasalazine, an inhibitor of the cystine-glutamate antiporter, reduces DNA damage repair and enhances radiosensitivity in murine B16F10 melanoma
inferredcites →https://doi.org/10.18632/oncotarget.16194openalex-snapshot
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inferredcites →https://doi.org/10.18632/oncotarget.25794openalex-snapshot
xCT inhibition sensitizes tumors to γ-radiation via glutathione reduction
inferredcites →https://doi.org/10.3109/10715762.2015.1129534openalex-snapshot
Radiation-induced autophagy: mechanisms and consequences
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inferredcites →https://doi.org/10.7554/elife.02523openalex-snapshot
Pharmacological inhibition of cystine–glutamate exchange induces endoplasmic reticulum stress and ferroptosis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116512openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116668openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ceramint.2024.01.024openalex-snapshot
Electrospun nanofibers combined with Fe-doped mesoporous bioactive glass nanoparticles induce in vitro melanoma cell death
inferred← citeshttps://doi.org/10.1016/j.chembiol.2020.03.013openalex-snapshot
The Chemistry and Biology of Ferroptosis
inferred← citeshttps://doi.org/10.1016/j.chembiol.2020.03.015openalex-snapshot
Progress in Understanding Ferroptosis and Challenges in Its Targeting for Therapeutic Benefit
inferred← citeshttps://doi.org/10.1016/j.chembiol.2023.04.007openalex-snapshot
Identification of structurally diverse FSP1 inhibitors that sensitize cancer cells to ferroptosis
inferred← citeshttps://doi.org/10.1016/j.cmet.2020.10.011openalex-snapshot
The Metabolic Underpinnings of Ferroptosis
inferred← citeshttps://doi.org/10.1016/j.craph.2026.100101openalex-snapshot
Radioprotective nanomedicines: New horizons in mitigating radiation-induced tissue injury
inferred← citeshttps://doi.org/10.1016/j.crbiot.2024.100205openalex-snapshot
Recent trends in nanozyme research and their potential therapeutic applications
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2022.103772openalex-snapshot
Puzzling out iron complications in cancer drug resistance
inferred← citeshttps://doi.org/10.1016/j.ctarc.2022.100545openalex-snapshot
Studying ferroptosis and pyroptosis as new cell death mechanisms induced by ionizing radiation in Ehrlich solid tumor-bearing mice
inferred← citeshttps://doi.org/10.1016/j.ctro.2024.100860openalex-snapshot
The oxygen puzzle in FLASH radiotherapy: A comprehensive review and experimental outlook
inferred← citeshttps://doi.org/10.1016/j.ctro.2025.101095openalex-snapshot
Pan-Cancer profiling of ferroptosis-related genes reveals prognostic biomarkers and sex-specific associations
inferred← citeshttps://doi.org/10.1016/j.drup.2023.101032openalex-snapshot
Upregulation of CoQ shifts ferroptosis dependence from GPX4 to FSP1 in acquired radioresistance
inferred← citeshttps://doi.org/10.1016/j.drup.2025.101250openalex-snapshot
Targeting SLC7A11 with sorafenib sensitizes stereotactic body radiotherapy in colorectal cancer liver metastasis
inferred← citeshttps://doi.org/10.1016/j.drup.2025.101293openalex-snapshot
HSA-templated synergistic platform boosts radiotherapy via enhanced radiosensitization and ferroptosis induction
inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.176124openalex-snapshot
Ferroptosis and tumor immunity: In perspective of the major cell components in the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132051openalex-snapshot
Supercritical CO2 extraction of fermented soybean lipids against erastin-induced ferroptosis in rat pheochromocytoma cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.08.029openalex-snapshot
Homocysteine induces oxidative stress and ferroptosis of nucleus pulposus via enhancing methylation of GPX4
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.01.002openalex-snapshot
Enhanced defense against ferroptosis ameliorates cognitive impairment and reduces neurodegeneration in 5xFAD mice
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.04.020openalex-snapshot
Lycium barbarum polysaccharide-glycoprotein ameliorates ionizing radiation-induced epithelial injury by regulating oxidative stress and ferroptosis via the Nrf2 pathway
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.01.029openalex-snapshot
IER3 promotes non-small cell lung cancer malignancy by suppressing ferroptosis via the AKT/GSK3β/NRF2 pathway
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.05.288openalex-snapshot
Carbon ions collapse the hypoxic lipid shield to decouple survival from redox vulnerability in NSCLC
inferred← citeshttps://doi.org/10.1016/j.gendis.2020.09.005openalex-snapshot
Ferroptosis: An emerging therapeutic opportunity for cancer
inferred← citeshttps://doi.org/10.1016/j.gendis.2020.11.010openalex-snapshot
NADPH debt drives redox bankruptcy: SLC7A11/xCT-mediated cystine uptake as a double-edged sword in cellular redox regulation
inferred← citeshttps://doi.org/10.1016/j.gendis.2024.101254openalex-snapshot
Regulation of SLC7A11 as an unconventional checkpoint in tumorigenesis through ferroptosis
inferred← citeshttps://doi.org/10.1016/j.gendis.2026.102370openalex-snapshot
Ferroptosis therapeutic modalities for glioblastoma: Molecular mechanisms, resistance reversal, and barrier overcoming
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145934openalex-snapshot
Identifying the key genes and functional enrichment pathways associated with feed efficiency in cattle
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e18950openalex-snapshot
Trends and hotspots of publications on ferroptosis: A 10 Year overview
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e19799openalex-snapshot
Ferroptosis, autophagy, tumor and immunity
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e19801openalex-snapshot
A bibliometric study and visualization analysis of ferroptosis-inducing cancer therapy
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39684openalex-snapshot
Improving understanding of ferroptosis: Molecular mechanisms, connection with cellular senescence and implications for aging
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.144742openalex-snapshot
CD38 inhibits ferroptosis to promote radiotherapy resistance in nasopharyngeal carcinoma by competitively binding to TRIM21 to stabilize SLC7A11 protein
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.150759openalex-snapshot
Aquaporin-4 mediated RONS transport under membrane lipid peroxidation: Atomic-scale mechanistic insights
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.111908openalex-snapshot
Intravenous immunoglobulin protects the integrity of the intestinal epithelial barrier and inhibits ferroptosis induced by radiation exposure by activating the mTOR pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112203openalex-snapshot
Ferroptosis in antitumor therapy: Unraveling regulatory mechanisms and immunogenic potential
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114597openalex-snapshot
Therapeutic and prognostic values of ferroptosis signature in glioblastoma
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115250openalex-snapshot
Nature's answer to Ferroptosis: how bioactive compounds rewire oxidative stress circuits in cerebral ischemia
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101617openalex-snapshot
Metabolic regulation of ferroptosis in the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.jddst.2020.101883openalex-snapshot
Ferroptotic nanomaterials enhance cancer therapy via boosting Fenton-reaction
inferred← citeshttps://doi.org/10.1016/j.jhep.2022.01.009openalex-snapshot
COMMD10 inhibits HIF1α/CP loop to enhance ferroptosis and radiosensitivity by disrupting Cu-Fe balance in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2024.578444openalex-snapshot
A ferroptosis-associated prognostic model correlated with immune landscape and radiotherapy response in low-grade gliomas (LGGs)
inferred← citeshttps://doi.org/10.1016/j.jocn.2026.112169openalex-snapshot
Clinical outcomes of ferroptosis-inducing agents in glioblastoma: A systematic review of clinical trials
inferred← citeshttps://doi.org/10.1016/j.lana.2024.100712openalex-snapshot
Long-term overall survival of patients who undergo breast-conserving therapy or mastectomy for early operable HER2-Positive breast cancer after preoperative systemic therapy: an observational cohort study
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119958openalex-snapshot
Cashing in on ferroptosis against tumor cells: Usher in the next chapter
inferred← citeshttps://doi.org/10.1016/j.lfs.2024.122629openalex-snapshot
Recent advancements in nanomaterial-mediated ferroptosis-induced cancer therapy: Importance of molecular dynamics and novel strategies
inferred← citeshttps://doi.org/10.1016/j.lmd.2026.100119openalex-snapshot
Reengineering immunotherapeutic responses: ferroptosis-primed radiotherapy converts cold-colorectal tumors into immunotherapy checkpoint inhibitor-sensitive hot lesions
inferred← citeshttps://doi.org/10.1016/j.matdes.2023.111613openalex-snapshot
Brigatinib-repurposed chemo-photodynamic therapy nanoplatform via effective apoptosis against colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.mcpro.2024.100888openalex-snapshot
Global Proteomics Indicates Subcellular-Specific Anti-Ferroptotic Responses to Ionizing Radiation
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.09.006openalex-snapshot
Amino Acids and Their Transporters in T Cell Immunity and Cancer Therapy
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.04.009openalex-snapshot
Unraveling ETC complex I function in ferroptosis reveals a potential ferroptosis-inducing therapeutic strategy for LKB1-deficient cancers
inferred← citeshttps://doi.org/10.1016/j.mtadv.2026.100693openalex-snapshot
Advance of different strategies to achieve radiosensitivity based on nanomaterials
inferred← citeshttps://doi.org/10.1016/j.mtbio.2025.101684openalex-snapshot
Bufotalin loaded biomimetic nanodrug for combined chemo/photodynamic therapy of cancer
inferred← citeshttps://doi.org/10.1016/j.mtnano.2025.100663openalex-snapshot
A cascade nanoreactor with ROS storms activation for amplified multimodal synergistic cancer therapy
inferred← citeshttps://doi.org/10.1016/j.nucana.2022.100024openalex-snapshot
Radiation target: Moving from theory to practice
inferred← citeshttps://doi.org/10.1016/j.oor.2026.100796openalex-snapshot
Targeting the angiotensin II/AT1R pathway and reactive oxygen species to mitigate oral mucositis: Mechanistic insights and therapeutic evidence
inferred← citeshttps://doi.org/10.1016/j.phrs.2021.105580openalex-snapshot
Regulation of ferroptosis by bioactive phytochemicals: Implications for medical nutritional therapy
inferred← citeshttps://doi.org/10.1016/j.radonc.2023.109689openalex-snapshot
Ferroptosis, necroptosis, and pyroptosis in cancer: Crucial cell death types in radiotherapy and post-radiotherapy immune activation
inferred← citeshttps://doi.org/10.1016/j.radonc.2026.111667openalex-snapshot
GSTM3 alleviates FLASH X-ray-induced testicular injury by modulating the ferroptosis pathway
inferred← citeshttps://doi.org/10.1016/j.radphyschem.2024.111887openalex-snapshot
Average dose rate is the primary determinant of lipid peroxidation in liposome membranes exposed to pulsed electron FLASH beam
inferred← citeshttps://doi.org/10.1016/j.radphyschem.2026.113838openalex-snapshot
FLASH irradiation does not induce lipid peroxidation in liposomes containing cholesterol and α-tocopherol
inferred← citeshttps://doi.org/10.1016/j.redox.2021.101928openalex-snapshot
PARP inhibition promotes ferroptosis via repressing SLC7A11 and synergizes with ferroptosis inducers in BRCA-proficient ovarian cancer
inferred← citeshttps://doi.org/10.1016/j.redox.2022.102413openalex-snapshot
NCOA4-mediated ferritinophagy is involved in ionizing radiation-induced ferroptosis of intestinal epithelial cells
inferred← citeshttps://doi.org/10.1016/j.redox.2023.102626openalex-snapshot
STC2 activates PRMT5 to induce radioresistance through DNA damage repair and ferroptosis pathways in esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.redox.2023.102677openalex-snapshot
Tubastatin A potently inhibits GPX4 activity to potentiate cancer radiotherapy through boosting ferroptosis
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103438openalex-snapshot
RSL3 sensitizes glioma cells to ionizing radiation by suppressing TGM2-dependent DNA damage repair and epithelial-mesenchymal transition
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103711openalex-snapshot
Radiation-induced upregulation of itaconate in macrophages promotes the radioresistance of non-small cell lung cancer by stabilizing NRF2 protein and suppressing immune response
inferred← citeshttps://doi.org/10.1016/j.redox.2025.103865openalex-snapshot
Carbon ion combined photon radiotherapy induces ferroptosis via NCOA4-mediated ferritinophagy in glioblastoma
inferred← citeshttps://doi.org/10.1016/j.tcb.2020.02.009openalex-snapshot
Emerging Mechanisms and Disease Relevance of Ferroptosis
inferred← citeshttps://doi.org/10.1016/j.tcb.2026.03.008openalex-snapshot
Ferroptosis as an approach to leverage cancer metabolism
inferred← citeshttps://doi.org/10.1016/j.toxicon.2025.108233openalex-snapshot
Ursolic acid enhances radiosensitivity in esophageal squamous cell carcinoma by modulating p53/SLC7A11/GPX4 pathway-mediated ferroptosis
inferred← citeshttps://doi.org/10.1016/j.tranon.2024.102251openalex-snapshot
EMC2 suppresses ferroptosis via regulating TFRC in nasopharyngeal carcinoma
inferred← citeshttps://doi.org/10.1016/j.tranon.2025.102393openalex-snapshot
Carfilzomib promotes Iodine-125 seed radiation-induced apoptosis, paraptosis, and ferroptosis in esophageal squamous cell carcinoma by aggravating endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.1016/j.trecan.2022.05.005openalex-snapshot
Radiotherapy-induced metabolic hallmarks in the tumor microenvironment
inferred← citeshttps://doi.org/10.1016/j.xcrm.2026.102745openalex-snapshot
A pig model of human radiation-induced veno-occlusive liver disease reveals ferroptosis as a therapeutic target
inferred← citeshttps://doi.org/10.1016/j.yexcr.2021.112932openalex-snapshot
Research progress on the mechanism of ferroptosis and its clinical application
inferred← citeshttps://doi.org/10.1016/j.yexcr.2021.112946openalex-snapshot
Hemin enhances radiosensitivity of lung cancer cells through ferroptosis
inferred← citeshttps://doi.org/10.1016/s0091-679x(22)00139-xopenalex-snapshot
Radiation therapy: An old dog learning new tricks
inferred← citeshttps://doi.org/10.1016/s0091-679x(23)00036-5openalex-snapshot
Radiation therapy: An old dog learning new tricks
inferred← citeshttps://doi.org/10.1016/s0091-679x(23)00166-8openalex-snapshot
Radiation therapy: An old dog learning new tricks
inferred← citeshttps://doi.org/10.1021/acs.analchem.5c02010openalex-snapshot
Single-Cell Lipidomics by LC-MS Interlaboratory Study Reveals the Impact of X-ray Irradiation on a Pancreatic Cancer Cell Line and Its Bystanders
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00546openalex-snapshot
Chemical Design of Magnetic Nanomaterials for Imaging and Ferroptosis-Based Cancer Therapy
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c01016openalex-snapshot
A Novel Redox Modulator Induces a GPX4-Mediated Cell Death That Is Dependent on Iron and Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c01749openalex-snapshot
Ferroptosis-Based Therapeutic Strategies toward Precision Medicine for Cancer
inferred← citeshttps://doi.org/10.1021/acs.jproteome.6c00317openalex-snapshot
Peroxiredoxin 6 Silencing Remodels Lipid Metabolism and Redox Pathways to Promote Ferroptosis-Mediated Radiosensitization in Nonsmall Cell Lung Cancer
inferred← citeshttps://doi.org/10.1021/acsami.4c21589openalex-snapshot
A Deferoxamine-Loaded Microneedle Patch Enhances Healing of Radiation-Induced Skin Injury: Potential Involvement of Ferroptosis
inferred← citeshttps://doi.org/10.1021/acsnano.3c00048openalex-snapshot
A MOF-Based Potent Ferroptosis Inducer for Enhanced Radiotherapy of Triple Negative Breast Cancer
inferred← citeshttps://doi.org/10.1021/acsnano.3c06967openalex-snapshot
A Multifunctional Covalent Organic Framework Nanozyme for Promoting Ferroptotic Radiotherapy against Esophageal Cancer
inferred← citeshttps://doi.org/10.1021/acsnano.4c02972openalex-snapshot
Radioactive Hydroxyapatite Microspheres Empower Sustainable In Situ Tumor Vaccination
inferred← citeshttps://doi.org/10.1021/acsnano.4c15932openalex-snapshot
Enhancing Ferroptosis-Mediated Radiosensitization via Synergistic Disulfidptosis Induction
inferred← citeshttps://doi.org/10.1021/acssensors.4c01455openalex-snapshot
Sensing Biomolecules Associated with Cells’ Radiosusceptibility by Advanced Micro- and Nanospectroscopy Techniques
inferred← citeshttps://doi.org/10.1038/s41374-022-00779-7openalex-snapshot
Inhibitory effects of temozolomide on glioma cells is sensitized by RSL3-induced ferroptosis but negatively correlated with expression of ferritin heavy chain 1 and ferritin light chain
inferred← citeshttps://doi.org/10.1038/s41388-021-01790-wopenalex-snapshot
Ferroptosis as a mechanism to mediate p53 function in tumor radiosensitivity
inferred← citeshttps://doi.org/10.1038/s41388-023-02744-0openalex-snapshot
The DUBA-SLC7A11-c-Myc Axis is Critical for Stemness and Ferroptosis
inferred← citeshttps://doi.org/10.1038/s41388-025-03368-2openalex-snapshot
Reciprocal regulation between ferroptosis and STING-type I interferon pathway suppresses head and neck squamous cell carcinoma growth through dendritic cell maturation
inferred← citeshttps://doi.org/10.1038/s41388-025-03585-9openalex-snapshot
Targeting ZNRF2-mediated SLC3A2 plasma membrane translocation enhances ferroptosis in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1038/s41391-024-00933-wopenalex-snapshot
Advances in ferroptosis for castration-resistant prostate cancer treatment: novel drug targets and combination therapy strategies
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