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RIP1 autophosphorylation is promoted by mitochondrial ROS and is essential for RIP3 recruitment into necrosome

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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.5520100210openalex-snapshot

Redox regulation of TNF signaling

inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05978.xopenalex-snapshot

Depletion of the mitochondrial electron transport abrogates the cytotoxic and gene‐inductive effects of TNF.

inferredcites →https://doi.org/10.1016/j.bbamcr.2016.09.012openalex-snapshot

Activation of apoptosis signalling pathways by reactive oxygen species

inferredcites →https://doi.org/10.1016/j.ccell.2015.10.001openalex-snapshot

NEMO Prevents Steatohepatitis and Hepatocellular Carcinoma by Inhibiting RIPK1 Kinase Activity-Mediated Hepatocyte Apoptosis

inferredcites →https://doi.org/10.1016/j.cell.2004.12.041openalex-snapshot

Reactive Oxygen Species Promote TNFα-Induced Death and Sustained JNK Activation by Inhibiting MAP Kinase Phosphatases

inferredcites →https://doi.org/10.1016/j.cell.2009.05.021openalex-snapshot

Receptor Interacting Protein Kinase-3 Determines Cellular Necrotic Response to TNF-α

inferredcites →https://doi.org/10.1016/j.cell.2009.05.037openalex-snapshot

Phosphorylation-Driven Assembly of the RIP1-RIP3 Complex Regulates Programmed Necrosis and Virus-Induced Inflammation

inferredcites →https://doi.org/10.1016/j.cell.2011.11.031openalex-snapshot

Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase

inferredcites →https://doi.org/10.1016/j.cell.2013.03.022openalex-snapshot

TNF Dually Mediates Resistance and Susceptibility to Mycobacteria via Mitochondrial Reactive Oxygen Species

inferredcites →https://doi.org/10.1016/j.celrep.2012.12.012openalex-snapshot

A Role of RIP3-Mediated Macrophage Necrosis in Atherosclerosis Development

inferredcites →https://doi.org/10.1016/j.celrep.2013.10.034openalex-snapshot

Widespread Mitochondrial Depletion via Mitophagy Does Not Compromise Necroptosis

inferredcites →https://doi.org/10.1016/j.celrep.2014.04.026openalex-snapshot

MLKL Compromises Plasma Membrane Integrity by Binding to Phosphatidylinositol Phosphates

inferredcites →https://doi.org/10.1016/j.chembiol.2005.05.018openalex-snapshot

A Functionally Orthogonal Estrogen Receptor-Based Transcription Switch Specifically Induced by a Nonsteroid Synthetic Ligand

inferredcites →https://doi.org/10.1016/j.chom.2015.01.002openalex-snapshot

RIP1/RIP3 Binding to HSV-1 ICP6 Initiates Necroptosis to Restrict Virus Propagation in Mice

inferredcites →https://doi.org/10.1016/j.leukres.2015.06.002openalex-snapshot

Differential changes in sphingolipids between TNF-induced necroptosis and apoptosis in U937 cells and necroptosis-resistant sublines

inferredcites →https://doi.org/10.1016/j.molcel.2014.03.003openalex-snapshot

Mixed Lineage Kinase Domain-like Protein MLKL Causes Necrotic Membrane Disruption upon Phosphorylation by RIP3

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

The Two Faces of Receptor Interacting Protein Kinase-1

inferredcites →https://doi.org/10.1016/j.molcel.2015.07.032openalex-snapshot

NF-κB-Independent Role of IKKα/IKKβ in Preventing RIPK1 Kinase-Dependent Apoptotic and Necroptotic Cell Death during TNF Signaling

inferredcites →https://doi.org/10.1016/j.str.2013.01.016openalex-snapshot

Structural Basis of RIP1 Inhibition by Necrostatins

inferredcites →https://doi.org/10.1016/j.tibs.2014.10.003openalex-snapshot

A new kind of cell suicide: mechanisms and functions of programmed necrosis

inferredcites →https://doi.org/10.1016/s0021-9258(18)42768-8openalex-snapshot

Cytotoxic activity of tumor necrosis factor is mediated by early damage of mitochondrial functions. Evidence for the involvement of mitochondrial radical generation.

inferredcites →https://doi.org/10.1038/cdd.2010.138openalex-snapshot

cIAP1 and TAK1 protect cells from TNF-induced necrosis by preventing RIP1/RIP3-dependent reactive oxygen species production

inferredcites →https://doi.org/10.1038/cdd.2013.94openalex-snapshot

RIPK3 contributes to TNFR1-mediated RIPK1 kinase-dependent apoptosis in conditions of cIAP1/2 depletion or TAK1 kinase inhibition

inferredcites →https://doi.org/10.1038/cdd.2014.70openalex-snapshot

RIPK1- and RIPK3-induced cell death mode is determined by target availability

inferredcites →https://doi.org/10.1038/cdd.2014.76openalex-snapshot

RIPK1 both positively and negatively regulates RIPK3 oligomerization and necroptosis

inferredcites →https://doi.org/10.1038/cdd.2014.77openalex-snapshot

Distinct roles of RIP1–RIP3 hetero- and RIP3–RIP3 homo-interaction in mediating necroptosis

inferredcites →https://doi.org/10.1038/cdd.2015.70openalex-snapshot

Characterization of RIPK3-mediated phosphorylation of the activation loop of MLKL during necroptosis

inferredcites →https://doi.org/10.1038/cr.2013.171openalex-snapshot

Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death

inferredcites →https://doi.org/10.1038/cr.2014.17openalex-snapshot

The Gβγ-Src signaling pathway regulates TNF-induced necroptosis via control of necrosome translocation

inferredcites →https://doi.org/10.1038/ncb2883openalex-snapshot

Plasma membrane translocation of trimerized MLKL protein is required for TNF-induced necroptosis

inferredcites →https://doi.org/10.1038/nchembio.83openalex-snapshot

Identification of RIP1 kinase as a specific cellular target of necrostatins

inferredcites →https://doi.org/10.1038/ni.2159openalex-snapshot

Programmed necrosis: backup to and competitor with apoptosis in the immune system

inferredcites →https://doi.org/10.1038/onc.2015.35openalex-snapshot

Reactive oxygen species regulate Smac mimetic/TNFα-induced necroptotic signaling and cell death

inferredcites →https://doi.org/10.1038/sj.cdd.4401746openalex-snapshot

Butylated hydroxyanisole is more than a reactive oxygen species scavenger

inferredcites →https://doi.org/10.1038/sj.cdd.4401754openalex-snapshot

Disulfide relays and phosphorylative cascades: partners in redox-mediated signaling pathways

inferredcites →https://doi.org/10.1042/bj20130860openalex-snapshot

Positive and negative phosphorylation regulates RIP1- and RIP3-induced programmed necrosis

inferredcites →https://doi.org/10.1073/pnas.1200012109openalex-snapshot

Mixed lineage kinase domain-like is a key receptor interacting protein 3 downstream component of TNF-induced necrosis

inferredcites →https://doi.org/10.1073/pnas.92.18.8115openalex-snapshot

Direct evidence for tumor necrosis factor-induced mitochondrial reactive oxygen intermediates and their involvement in cytotoxicity.

inferredcites →https://doi.org/10.1074/jbc.m112.435545openalex-snapshot

Diverse Sequence Determinants Control Human and Mouse Receptor Interacting Protein 3 (RIP3) and Mixed Lineage Kinase domain-Like (MLKL) Interaction in Necroptotic Signaling

inferredcites →https://doi.org/10.1074/jbc.m313141200openalex-snapshot

Tumor Necrosis Factor-induced Nonapoptotic Cell Death Requires Receptor-interacting Protein-mediated Cellular Reactive Oxygen Species Accumulation

inferredcites →https://doi.org/10.1074/mcp.m112.019091openalex-snapshot

Investigation of Receptor interacting protein (RIP3)-dependent Protein Phosphorylation by Quantitative Phosphoproteomics

inferredcites →https://doi.org/10.1093/nar/25.20.4165openalex-snapshot

Ligation independent cloning irrespective of restriction site compatibility

inferredcites →https://doi.org/10.1126/science.1172308openalex-snapshot

RIP3, an Energy Metabolism Regulator That Switches TNF-Induced Cell Death from Apoptosis to Necrosis

inferredcites →https://doi.org/10.1126/science.1249361openalex-snapshot

Activity of Protein Kinase RIPK3 Determines Whether Cells Die by Necroptosis or Apoptosis

inferredcites →https://doi.org/10.1126/science.aaa2630openalex-snapshot

Phosphorylation of innate immune adaptor proteins MAVS, STING, and TRIF induces IRF3 activation

inferredcites →https://doi.org/10.1146/annurev-immunol-032414-112248openalex-snapshot

Programmed Necrosis in the Cross Talk of Cell Death and Inflammation

inferredcites →https://doi.org/10.1146/annurev-physiol-021113-170259openalex-snapshot

Control of Life-or-Death Decisions by RIP1 Kinase

inferredcites →https://doi.org/10.1371/journal.pone.0076841openalex-snapshot

CYLD Deubiquitinates RIP1 in the TNFα-Induced Necrosome to Facilitate Kinase Activation and Programmed Necrosis

inferredcites →https://doi.org/10.4049/jimmunol.1400499openalex-snapshot

Cutting Edge: RIP1 Kinase Activity Is Dispensable for Normal Development but Is a Key Regulator of Inflammation in SHARPIN-Deficient Mice

What points at this work

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

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Systemic LPS-Induced RACK1 Downregulation Contributes to Neuronal Necroptosis in the Limbic System in Mice: A Mechanism of Sepsis-Associated Encephalopathy and a Potential Target of Tanshinone IIA

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Targeting RIPK3 oligomerization blocks necroptosis without inducing apoptosis

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PANoptosis in the pathogenesis of myelodysplastic syndromes

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Fe(III)‐Shikonin Supramolecular Nanomedicine for Combined Therapy of Tumor via Ferroptosis and Necroptosis

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Ultrasound‐Driven Non‐Metallic Fenton‐Active Center Construction for Extensive Chemodynamic Therapy

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Ultrasmall Enzyodynamic PANoptosis Nano‐Inducers for Ultrasound‐Amplified Hepatocellular Carcinoma Therapy and Lung Metastasis Inhibition

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Nanoshield‐Assisted Viral Gene Therapy with Induction of Non‐Apoptotic Cell Death and Durable Antitumor Immunity

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Procyanidin Capsules Combat ALF by Restoring Mitochondrial Homeostasis and Inhibiting Necroptosis via the PGAM5/DRP1/PINK1 Pathway

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Fisetin, a phytopolyphenol, targets apoptotic and necroptotic cell death in HepG2 cells

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The potential protective effect of liraglutide on valproic acid induced liver injury in rats: Targeting HMGB1/RAGE axis and RIPK3/MLKL mediated necroptosis

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Reactive Oxygen Species (ROS) and Their Profound Influence on Regulating Diverse Aspects of Cancer: A Concise Review

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RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease

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Piperlongumine increases the sensitivity of bladder cancer to cisplatin by mitochondrial ROS

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Inhibition of HSP90α protects cultured neurons from oxygen‐glucose deprivation induced necroptosis by decreasing RIP3 expression

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Trimethylamine N‐oxide promotes apoE−/− mice atherosclerosis by inducing vascular endothelial cell pyroptosis via the SDHB/ROS pathway

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Lysosome signaling in cell survival and programmed cell death for cellular homeostasis

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Multiple forms of cell death: A focus on the PI3K/AKT pathway

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Amelioration of inflammatory myopathies by glucagon‐like peptide‐1 receptor agonist via suppressing muscle fibre necroptosis

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Death‐Associated Protein 3 Triggers Intrinsic Apoptosis via Miro1 Upon Inducing Intracellular Calcium Changes

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Dissecting the pleiotropic roles of reactive oxygen species (ROS) in lung cancer: From carcinogenesis toward therapy

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β‐Caryophyllene Mitigates Thioacetamide‐Induced Liver Fibrosis Through CB2 ‐Mediated Suppression of Necroptosis: A Therapeutic Investigation

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Pitavastatin and metformin synergistically activate apoptosis and autophagy in pancreatic cancer cells

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Protective effect of C‐phycocyanin and apo‐phycocyanin subunit on programmed necrosis of GC ‐1 spg cells induced by H2O2

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Polystyrene nanoplastics exacerbated lipopolysaccharide‐induced necroptosis and inflammation via the ROS / MAPK pathway in mice spleen

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Unraveling the intriguing interplay: Exploring the role of lncRNAs in caspase‐independent cell death

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Cancer-Associated Programmed Cell Death Mechanisms: Extended with Biochemical Markers and Experimental Approaches

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Induction and Detection of Necroptotic Cell Death in Mammalian Cell Culture

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Necroptosis, the Other Main Caspase-Independent Cell Death

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Modulation of Necroptosis by Micronutrients: Experimental Evidence and Possible Effects Interfering with Necroptotic Signaling

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usEP Induce Regulated Cell Death Mechanisms

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The Double-Edged Sword Role of ROS in Cancer

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The Double-Edged Sword Role of ROS in Cancer

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Recent Advances in Oxidative Stress Associated Chronic Diseases

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ROS/Redox Signaling and Apoptosis/Necroptosis/Autophagy in Cancer

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Homer1 ameliorates ischemic stroke by inhibiting necroptosis-induced neuronal damage and neuroinflammation

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RIPK3 signaling and its role in the pathogenesis of cancers

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Inflammation suppression in doxorubicin-induced cardiotoxicity: natural compounds as therapeutic options

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Oxidative stress dynamics during the estrous cycle: histological and biochemical findings in a rat model

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Induction of reactive oxygen species: an emerging approach for cancer therapy

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MLKL mediates apoptosis via a mutual regulation with PERK/eIF2α pathway in response to reactive oxygen species generation

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Flow cytometric detection of hyper-polarized mitochondria in regulated and accidental cell death processes

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Triptolide induces PANoptosis in macrophages and causes organ injury in mice

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Necroptosis in obesity: a complex cell death event

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Interaction of HIF-1a with various cell death pathways in tumor immune microenvironment (TIME)

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Oxidative Stress-Mediated Programmed Cell Death: a Potential Therapy Target for Atherosclerosis

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Rubiarbonol B induces RIPK1-dependent necroptosis via NOX1-derived ROS production

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Redox processes in the treatment of advanced skin cancers

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From RIPK1 to Necroptosis: Pathogenic Mechanisms in Neurodegenerative Diseases

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Chlorpyrifos induces apoptosis and necroptosis via the activation of CYP450s pathway mediated by nuclear receptors in LMH cells

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RIPK1: A Promising Target for Intervention Neuroinflammation

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Bee venom induces anti-tumor effects in HT-29 colon cancer cells through regulation of cell proliferation and apoptosis

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Selenium Prevents Lead-Induced Necroptosis by Restoring Antioxidant Functions and Blocking MAPK/NF-κB Pathway in Chicken Lymphocytes

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The Alleviative Effects of Quercetin on Cadmium-Induced Necroptosis via Inhibition ROS/iNOS/NF-κB Pathway in the Chicken Brain

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Rutin Ameliorates Cadmium-Induced Necroptosis in the Chicken Liver via Inhibiting Oxidative Stress and MAPK/NF-κB Pathway

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Loss of Microglial Parkin Inhibits Necroptosis and Contributes to Neuroinflammation

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Aging-Dependent Mitophagy Dysfunction in Alzheimer’s Disease

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Acute Administration of Edaravone Improves Cognitive Impairment in a Mouse Model of mPFC Ischemia: Crosstalk Between Necroptosis, Neuroinflammation, and Antioxidant Defense

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Integrated Necroptosis Within Programmed Cell Death in Traumatic Brain Injury

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The development of necroptosis: what we can learn

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Oxidative Stress and Potential Antioxidant Therapies in Vitiligo: A Narrative Review

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N-Acetylcysteine Attenuates Epirubicin-Induced Neurobehavioral, Inflammatory, and Neuroplasticity-Related Alterations in Rats

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Molecular mechanisms of cell death

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Physiology of cellular demise: Apoptosis, necrosis, and autophagy

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Tuning the way to die: implications of membrane perturbations in necroptosis

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Redox, cysteines, and kinases—A triad sustaining myeloid leukemia

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Molecular mechanisms of necroptosis and relevance for neurodegenerative diseases

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Necroptosis, ADAM proteases and intestinal (dys)function

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Role and relation of cell death in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.aanat.2023.152049openalex-snapshot

Inhibition of mitochondrial VDAC1 oligomerization alleviates apoptosis and necroptosis of retinal neurons following OGD/R injury

inferred← citeshttps://doi.org/10.1016/j.apsb.2020.07.003openalex-snapshot

The role of lysosome in regulated necrosis

inferred← citeshttps://doi.org/10.1016/j.apsb.2025.09.002openalex-snapshot

DNAzyme targeting RIP3 suppresses NLRP3-mediated necroinflammation for the treatment of inflammatory diseases

inferred← citeshttps://doi.org/10.1016/j.aquatox.2024.107190openalex-snapshot

TBBPA caused multiple intestinal injuries via ROS/NF-κB signal in common carp

inferred← citeshttps://doi.org/10.1016/j.arr.2021.101263openalex-snapshot

Oxidative stress and regulated cell death in Parkinson’s disease

inferred← citeshttps://doi.org/10.1016/j.arr.2023.101855openalex-snapshot

Unwinding the modalities of necrosome activation and necroptosis machinery in neurological diseases

inferred← citeshttps://doi.org/10.1016/j.arr.2025.102770openalex-snapshot

Mechanism of ferroptosis in heart failure: The role of the RAGE/TLR4-JNK1/2 pathway in cardiomyocyte ferroptosis and intervention strategies

inferred← citeshttps://doi.org/10.1016/j.bbadis.2023.166922openalex-snapshot

Reactive oxygen species in colorectal cancer adjuvant therapies

inferred← citeshttps://doi.org/10.1016/j.bbadis.2025.167828openalex-snapshot

The function of necroptosis in liver cancer

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.05.025openalex-snapshot

Proteolytic control of regulated necrosis

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118826openalex-snapshot

MiR-7 mediates mitochondrial impairment to trigger apoptosis and necroptosis in Rhabdomyosarcoma

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119534openalex-snapshot

Novel, non-conventional pathways of necroptosis in the heart and other organs: Molecular mechanisms, regulation and inter-organelle interplay

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119722openalex-snapshot

Redox signaling in cell fate: Beyond damage

inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188705openalex-snapshot

Metabolic tricks of cancer cells

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.06.019openalex-snapshot

Effects of intracellular iron overload on cell death and identification of potent cell death inhibitors

inferred← citeshttps://doi.org/10.1016/j.bcp.2023.115938openalex-snapshot

The critical roles of STING in mitochondrial homeostasis

inferred← citeshttps://doi.org/10.1016/j.bcp.2025.116951openalex-snapshot

Necroptosis: a significant and promising target for intervention of cardiovascular disease

inferred← citeshttps://doi.org/10.1016/j.bcp.2025.117021openalex-snapshot

Anti-inflammatory mechanism of the MLKL inhibitor necrosulfonamide in LPS- or poly(I:C)-induced neuroinflammation and necroptosis

inferred← citeshttps://doi.org/10.1016/j.bcp.2026.117843openalex-snapshot

Cabozantinib inhibits necroptosis by targeting MLKL oligomerization and alleviates psoriasis in vivo

inferred← citeshttps://doi.org/10.1016/j.bcp.2026.118230openalex-snapshot

Targeting RIPK1 for the treatment of depression: From neuroinflammation to synaptic plasticity

inferred← citeshttps://doi.org/10.1016/j.biomaterials.2024.123001openalex-snapshot

In-situ Sprayed platelet-derived small extracellular vesicles for the skin flap survival by reducing PANoptosis

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108304openalex-snapshot

Quinazoline-2,4(1H,3H)-dione modulates STAT3 and FOXO3a signaling in HepG2 cells

inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109019openalex-snapshot

RIP3 inhibition protects locomotion function through ameliorating mitochondrial antioxidative capacity after spinal cord injury

inferred← citeshttps://doi.org/10.1016/j.biopha.2019.109784openalex-snapshot

Irigenin treatment alleviates doxorubicin (DOX)-induced cardiotoxicity by suppressing apoptosis, inflammation and oxidative stress via the increase of miR-425

inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112082openalex-snapshot

The latest information on the RIPK1 post-translational modifications and functions

inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113806openalex-snapshot

Ferroptosis: A new strategy for traditional Chinese medicine treatment of stroke

inferred← citeshttps://doi.org/10.1016/j.biopha.2022.113982openalex-snapshot

Eleutheroside B ameliorated high altitude pulmonary edema by attenuating ferroptosis and necroptosis through Nrf2-antioxidant response signaling

inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116690openalex-snapshot

The role of mitochondrial damage-associated molecular patterns in acute pancreatitis

inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118335openalex-snapshot

Crosstalk between mitochondrial quality control and novel programmed cell death in pulmonary diseases

inferred← citeshttps://doi.org/10.1016/j.biopha.2025.118349openalex-snapshot

Mitochondrial homeostasis: Exploring their impact on skin disease pathogenesis

inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118241openalex-snapshot

Oxidative complexity: The role of ROS in the tumor environment and therapeutic implications

inferred← citeshttps://doi.org/10.1016/j.brainres.2019.05.018openalex-snapshot

Renal ischemia/reperfusion induced learning and memory deficit in the rat: Insights into underlying molecular and cellular mechanisms

inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111387openalex-snapshot

The interactive toxic effect of homocysteine and copper on cardiac microvascular endothelial cells during ischemia-reperfusion injury

inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111758openalex-snapshot

Mechanisms and targeted prevention of chronic pancreatitis-acinar to ductal metaplasia caused by a low concentration of di-(2-ethylhexyl)-phthalate

inferred← citeshttps://doi.org/10.1016/j.ceb.2020.02.004openalex-snapshot

New insights into the regulation of apoptosis, necroptosis, and pyroptosis by receptor interacting protein kinase 1 and caspase-8

inferred← citeshttps://doi.org/10.1016/j.cej.2024.159202openalex-snapshot

A Shikonin-Iron-Tragacanth gum nanocomplex for synergistic treatment of bladder cancer

inferred← citeshttps://doi.org/10.1016/j.celrep.2018.01.089openalex-snapshot

Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson’s Disease Models

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114641openalex-snapshot

Non-canonical autophosphorylation of RIPK1 drives timely pyroptosis to control Yersinia infection

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114966openalex-snapshot

Residue Y362 is crucial for FLIPL to impart catalytic activity to pro-caspase-8 to suppress necroptosis

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115804openalex-snapshot

Cell death and cancer: Metabolic interconnections

inferred← citeshttps://doi.org/10.1016/j.cmet.2023.07.001openalex-snapshot

Tumor aerobic glycolysis confers immune evasion through modulating sensitivity to T cell-mediated bystander killing via TNF-α

inferred← citeshttps://doi.org/10.1016/j.coi.2023.102366openalex-snapshot

Mitochondrial reactive oxygen species: double agents in Mycobacterium tuberculosis infection

inferred← citeshttps://doi.org/10.1016/j.copbio.2020.10.004openalex-snapshot

Virus-induced metabolic reprogramming and innate sensing hereof by the infected host

inferred← citeshttps://doi.org/10.1016/j.critrevonc.2024.104361openalex-snapshot

The involvement of ROS-regulated programmed cell death in hepatocellular carcinoma

inferred← citeshttps://doi.org/10.1016/j.cyto.2020.155046openalex-snapshot

PI3K mediates tumor necrosis factor induced-necroptosis through initiating RIP1-RIP3-MLKL signaling pathway activation

inferred← citeshttps://doi.org/10.1016/j.devcel.2021.03.033openalex-snapshot

Mechanistic connections between mitochondrial biology and regulated cell death

inferred← citeshttps://doi.org/10.1016/j.drudis.2024.104020openalex-snapshot

The role of RIPK1 in chronic obstructive pulmonary disease

inferred← citeshttps://doi.org/10.1016/j.drup.2024.101170openalex-snapshot

Autophagy in cancer development, immune evasion, and drug resistance

inferred← citeshttps://doi.org/10.1016/j.drup.2026.101387openalex-snapshot

Programmed cell death network in cancer drug resistance: A framework for therapeutic intervention

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.110064openalex-snapshot

Astilbin protects chicken peripheral blood lymphocytes from cadmium-induced necroptosis via oxidative stress and the PI3K/Akt pathway

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111049openalex-snapshot

The antagonistic effect of selenium on lead-induced necroptosis via MAPK/NF-κB pathway and HSPs activation in the chicken spleen

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115089openalex-snapshot

Perfluorooctanoic acid-induced cell death via the dual roles of ROS-MAPK/ERK signaling in ameloblast-lineage cells

inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114557openalex-snapshot

Influence of chain length on the anticancer activity of the antimicrobial peptide CAMEL with fatty acid modification

inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116123openalex-snapshot

RIPK1 inhibitors: A key to unlocking the potential of necroptosis in drug development

inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117530openalex-snapshot

Discovery of phenylisoxazolidine analogs targeting receptor interacting protein kinase 1 with anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.174840openalex-snapshot

RETRA induces necroptosis in cervical cancer cells through RIPK1, RIPK3, MLKL and increased ROS production

inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.175213openalex-snapshot

Morin offsets PTZ-induced neuronal degeneration and cognitive decrements in rats: The modulation of TNF-α/TNFR-1/RIPK1,3/MLKL/PGAM5/Drp-1, IL-6/JAK2/STAT3/GFAP and Keap-1/Nrf-2/HO-1 trajectories

inferred← citeshttps://doi.org/10.1016/j.ejphar.2023.175537openalex-snapshot

Natural and synthetic compounds for glioma treatment based on ROS-mediated strategy

inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.176508openalex-snapshot

Protein phosphorylation and kinases: Potential therapeutic targets in necroptosis

inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.176736openalex-snapshot

Chronic mitochondrial dynamic-targeted therapy alleviates left ventricular dysfunction by reducing multiple programmed cell death in post-myocardial infarction rats

inferred← citeshttps://doi.org/10.1016/j.envint.2024.108771openalex-snapshot

Co-exposure of microcystin and nitrite enhanced spermatogenic disorders: The role of mtROS-mediated pyroptosis and apoptosis

inferred← citeshttps://doi.org/10.1016/j.fct.2024.114525openalex-snapshot

3-Monochloropropane-1,2-diol esters induce HepG2 cells necroptosis via CTSB/TFAM/ROS pathway

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.12.034openalex-snapshot

Loss of RIP3 initiates annihilation of high-fat diet initialized nonalcoholic hepatosteatosis: A mechanism involving Toll-like receptor 4 and oxidative stress

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.01.008openalex-snapshot

Redox biology of regulated cell death in cancer: A focus on necroptosis and ferroptosis

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.07.025openalex-snapshot

Iron deficiency exacerbates cisplatin- or rhabdomyolysis-induced acute kidney injury through promoting iron-catalyzed oxidative damage

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.11.008openalex-snapshot

Activation of UQCRC2-dependent mitophagy by tetramethylpyrazine inhibits MLKL-mediated hepatocyte necroptosis in alcoholic liver disease

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.03.021openalex-snapshot

Necroptosis signaling and mitochondrial dysfunction cross-talking facilitate cell death mediated by chelerythrine in glioma

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.07.022openalex-snapshot

p53 at the crossroad between mitochondrial reactive oxygen species and necroptosis

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.06.006openalex-snapshot

Redox signaling in innate immunity and inflammation: focus on macrophages and neutrophils

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.07.036openalex-snapshot

Dehydroascorbic acid impairs neurite growth through RIPK1-associated caspase activation

inferred← citeshttps://doi.org/10.1016/j.fsi.2022.09.062openalex-snapshot

Tannic acid through ROS/TNF-α/TNFR 1 antagonizes atrazine induced apoptosis, programmed necrosis and immune dysfunction of grass carp hepatocytes

inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109802openalex-snapshot

Modulatory effects of necroptosis: A potential preventive approach to control diseases in fish

inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109850openalex-snapshot

Myo-inositol: A potential game-changer in preventing gill cell death and alleviating “gill rot” in grass carp (Ctenopharyngodon idellus)

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.e21231openalex-snapshot

Vaccarin alleviates cisplatin-induced acute kidney injury via decreasing NOX4-derived ROS

inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e21889openalex-snapshot

Sugarcane leaf polysaccharide exerts a therapeutic effect on cardiovascular diseases through necroptosis

inferred← citeshttps://doi.org/10.1016/j.ifset.2025.103964openalex-snapshot

Antifungal and anti-aflatoxigenic mechanisms of dielectric barrier discharge cold plasma on Aspergillus flavus spores

inferred← citeshttps://doi.org/10.1016/j.intimp.2023.109974openalex-snapshot

Celastrol inhibits necroptosis by attenuating the RIPK1/RIPK3/MLKL pathway and confers protection against acute pancreatitis in mice

inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110603openalex-snapshot

Necroptosis in the sarcoma immune microenvironment: From biology to therapy

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112616openalex-snapshot

Spotlight on necroptosis: Role in pathogenesis and therapeutic potential of intervertebral disc degeneration

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113240openalex-snapshot

Review of research progress on different modalities of Macrophage death in Mycobacterium leprae infection

inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114761openalex-snapshot

Theaflavin suppresses necroptosis by attenuating RIPK1-RIPK3-MLKL signaling and mitigates cisplatin-induced kidney injury in mice

inferred← citeshttps://doi.org/10.1016/j.intimp.2025.115558openalex-snapshot

YAP ameliorates CCl4-induced acute liver injury by activating autophagy via modulating p300/CBP-mediated FoxO3 acetylation

inferred← citeshttps://doi.org/10.1016/j.it.2022.02.002openalex-snapshot

Context-dependent regulation of follicular helper T cell survival

inferred← citeshttps://doi.org/10.1016/j.it.2026.03.006openalex-snapshot

Exploiting immunogenic cell death to promote antitumor immunity

inferred← citeshttps://doi.org/10.1016/j.jad.2025.01.135openalex-snapshot

Association between depressive symptoms and premature death: An exploratory mediation analysis via mitochondrial function

inferred← citeshttps://doi.org/10.1016/j.jare.2023.11.004openalex-snapshot

ASIC1/RIP1 accelerates atherosclerosis via disrupting lipophagy

inferred← citeshttps://doi.org/10.1016/j.jcmgh.2019.10.002openalex-snapshot

RIPK1 Mediates TNF-Induced Intestinal Crypt Apoptosis During Chronic NF-κB Activation

inferred← citeshttps://doi.org/10.1016/j.jcmgh.2019.10.009openalex-snapshot

Tumor Necrosis Factor-α–Induced Apoptosis in the Intestinal Epithelium due to Chronic Nuclear Factor Kappa B Signaling Is Mediated by Receptor Interacting Serine/Threonine Kinase 1

inferred← citeshttps://doi.org/10.1016/j.jep.2024.118253openalex-snapshot

Inhibition of mitochondrial ROS-mediated necroptosis by Dendrobium nobile Lindl. alkaloids in carbon tetrachloride induced acute liver injury

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133719openalex-snapshot

Sodium sulfite triggered hepatic apoptosis, necroptosis, and pyroptosis by inducing mitochondrial damage in mice and AML-12 cells

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.140685openalex-snapshot

Citrinin induces renal PANoptosis by mediating mitochondrial dysfunction through the GSDMD-N/DRP1 pathway

inferred← citeshttps://doi.org/10.1016/j.jhep.2018.01.026openalex-snapshot

Fibroblast growth factor receptor inhibition induces loss of matrix MCL1 and necrosis in cholangiocarcinoma

inferred← citeshttps://doi.org/10.1016/j.jid.2020.06.042openalex-snapshot

RIP1-Mediated Necroptosis Facilitates Oxidative Stress‒Induced Melanocyte Death, Offering Insight into Vitiligo

inferred← citeshttps://doi.org/10.1016/j.jnutbio.2022.109052openalex-snapshot

Excess fructose enhances oleatic cytotoxicity via reactive oxygen species production and causes necroptosis in hepatocytes

inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119963openalex-snapshot

Intermittent hypoxia aggravates non-alcoholic fatty liver disease via RIPK3-dependent necroptosis-modulated Nrf2/NFκB signaling pathway

inferred← citeshttps://doi.org/10.1016/j.lfs.2026.124456openalex-snapshot

The death code in nanomessengers: Mechanisms and advances in the regulation of programmed cell death by exosomes

inferred← citeshttps://doi.org/10.1016/j.metabol.2024.155975openalex-snapshot

Intricate interplay between cell metabolism and necroptosis regulation in metabolic dysfunction-associated steatotic liver disease: A narrative review

inferred← citeshttps://doi.org/10.1016/j.mito.2020.12.004openalex-snapshot

Altered mitochondrial calcium handling and cell death by necroptosis: An emerging paradigm

inferred← citeshttps://doi.org/10.1016/j.mito.2024.101957openalex-snapshot

The multifaceted effects of mitochondria in kidney diseases

inferred← citeshttps://doi.org/10.1016/j.mvr.2023.104565openalex-snapshot

Myocardial ischemia-reperfusion injury; Molecular mechanisms and prevention

inferred← citeshttps://doi.org/10.1016/j.nbd.2025.106907openalex-snapshot

Molecular mechanism of PANoptosis and programmed cell death in neurological diseases

inferred← citeshttps://doi.org/10.1016/j.neulet.2020.135565openalex-snapshot

RIP3-mediated necroptosis was essential for spiral ganglion neuron damage

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2026.04.031openalex-snapshot

PANoptosis: an emerging programmed cell death pathway in neurological diseases mechanisms and therapeutic translation

inferred← citeshttps://doi.org/10.1016/j.pan.2021.01.010openalex-snapshot

Combating pancreatic cancer chemoresistance by triggering multiple cell death pathways

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