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MAPK15 protects from oxidative stress‐dependent cellular senescence by inducing the mitophagic process

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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/jcp.27053openalex-snapshot
Regulation of human mitogen‐activated protein kinase 15 (extracellular signal‐regulated kinase 7/8) and its functions: A recent update
inferredcites →https://doi.org/10.1006/scdb.2001.0282openalex-snapshot
Reactive oxygen species and mitochondrial diseases
inferredcites →https://doi.org/10.1016/j.bbadis.2018.09.018openalex-snapshot
Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy
inferredcites →https://doi.org/10.1016/j.ccr.2006.08.009openalex-snapshot
Selective killing of oncogenically transformed cells through a ROS-mediated mechanism by β-phenylethyl isothiocyanate
inferredcites →https://doi.org/10.1016/j.cell.2009.02.024openalex-snapshot
Principles of Cancer Therapy: Oncogene and Non-oncogene Addiction
inferredcites →https://doi.org/10.1016/j.celrep.2014.06.043openalex-snapshot
A Mitochondrial Switch Promotes Tumor Metastasis
inferredcites →https://doi.org/10.1016/j.celrep.2017.12.092openalex-snapshot
Cellular Senescence Is Induced by the Environmental Neurotoxin Paraquat and Contributes to Neuropathology Linked to Parkinson’s Disease
inferredcites →https://doi.org/10.1016/j.celrep.2021.109441openalex-snapshot
The Cancer SENESCopedia: A delineation of cancer cell senescence
inferredcites →https://doi.org/10.1016/j.febslet.2009.01.011openalex-snapshot
Regulation of the activity and expression of ERK8 by DNA damage
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2021.07.004openalex-snapshot
MAPK15-ULK1 signaling regulates mitophagy of airway epithelial cell in chronic obstructive pulmonary disease
inferredcites →https://doi.org/10.1016/j.molcel.2015.10.009openalex-snapshot
Measuring In Vivo Mitophagy
inferredcites →https://doi.org/10.1038/295334a0openalex-snapshot
Reorganization of HeLa cell cytoskeleton induced by an uncoupler of oxidative phosphorylation
inferredcites →https://doi.org/10.1038/cdd.2014.139openalex-snapshot
AMBRA1 is able to induce mitophagy via LC3 binding, regardless of PARKIN and p62/SQSTM1
inferredcites →https://doi.org/10.1038/msb.2010.5openalex-snapshot
Feedback between p21 and reactive oxygen production is necessary for cell senescence
inferredcites →https://doi.org/10.1038/nature16187openalex-snapshot
Autophagy maintains stemness by preventing senescence
inferredcites →https://doi.org/10.1038/ncb2012openalex-snapshot
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
inferredcites →https://doi.org/10.1038/ncb2466openalex-snapshot
Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation
inferredcites →https://doi.org/10.1038/ncomms1708openalex-snapshot
Telomeres are favoured targets of a persistent DNA damage response in ageing and stress-induced senescence
inferredcites →https://doi.org/10.1038/nrm.2017.66openalex-snapshot
Mitochondrial diseases: the contribution of organelle stress responses to pathology
inferredcites →https://doi.org/10.1038/s41580-020-00314-wopenalex-snapshot
Cellular senescence in ageing: from mechanisms to therapeutic opportunities
inferredcites →https://doi.org/10.1073/pnas.0911187107openalex-snapshot
PINK1-dependent recruitment of Parkin to mitochondria in mitophagy
inferredcites →https://doi.org/10.1074/jbc.m110.179523openalex-snapshot
Extracellular Signal-regulated Kinase 8 (ERK8) Controls Estrogen-related Receptor α (ERRα) Cellular Localization and Inhibits Its Transcriptional Activity
inferredcites →https://doi.org/10.1074/jbc.m210432200openalex-snapshot
Mitochondrial Complex I Inhibitor Rotenone Induces Apoptosis through Enhancing Mitochondrial Reactive Oxygen Species Production
inferredcites →https://doi.org/10.1074/jbc.m513397200openalex-snapshot
Activation of the Erk8 Mitogen-activated Protein (MAP) Kinase by RET/PTC3, a Constitutively Active Form of the RET Proto-oncogene
inferredcites →https://doi.org/10.1074/jbc.ra118.002527openalex-snapshot
MAPK15 is part of the ULK complex and controls its activity to regulate early phases of the autophagic process
inferredcites →https://doi.org/10.1080/15548627.2015.1084454openalex-snapshot
MAPK15 mediates BCR-ABL1-induced autophagy and regulates oncogene-dependent cell proliferation and tumor formation
inferredcites →https://doi.org/10.1080/15548627.2020.1797280openalex-snapshot
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1
inferredcites →https://doi.org/10.1083/jcb.201002124openalex-snapshot
A chromatin-bound kinase, ERK8, protects genomic integrity by inhibiting HDM2-mediated degradation of the DNA clamp PCNA
inferredcites →https://doi.org/10.1111/acel.13211openalex-snapshot
Dependence of PINK1 accumulation on mitochondrial redox system
inferredcites →https://doi.org/10.1111/acel.13620openalex-snapshot
MAPK15 protects from oxidative stress‐dependent cellular senescence by inducing the mitophagic process
inferredcites →https://doi.org/10.1111/febs.15570openalex-snapshot
A guide to assessing cellular senescence in vitro and in vivo
inferredcites →https://doi.org/10.1111/j.1365-2443.2010.01426.xopenalex-snapshot
p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
inferredcites →https://doi.org/10.1126/sciadv.abg4544openalex-snapshot
AMPK/ULK1-mediated phosphorylation of Parkin ACT domain mediates an early step in mitophagy
inferredcites →https://doi.org/10.1152/physrev.1979.59.3.527openalex-snapshot
Hydroperoxide metabolism in mammalian organs.
inferredcites →https://doi.org/10.1158/0008-5472.can-10-2734openalex-snapshot
High-Throughput RNAi Screening Reveals Novel Regulators of Telomerase
inferredcites →https://doi.org/10.14348/molcells.2018.2277openalex-snapshot
A Molecular Approach to Mitophagy and Mitochondrial Dynamics.
inferredcites →https://doi.org/10.1523/jneurosci.1917-11.2011openalex-snapshot
Parkin Interacts with Ambra1 to Induce Mitophagy
inferredcites →https://doi.org/10.18632/oncotarget.8044openalex-snapshot
MAPK15 upregulation promotes cell proliferation and prevents DNA damage in male germ cell tumors
inferredcites →https://doi.org/10.3389/fcell.2020.00171openalex-snapshot
Mammalian Mitophagosome Formation: A Focus on the Early Signals and Steps
inferredcites →https://doi.org/10.3389/fonc.2018.00548openalex-snapshot
Quantitative Proteomic Analysis Identifies MAPK15 as a Potential Regulator of Radioresistance in Nasopharyngeal Carcinoma Cells
inferredcites →https://doi.org/10.3390/cells11010030openalex-snapshot
Mitophagy: Molecular Mechanisms, New Concepts on Parkin Activation and the Emerging Role of AMPK/ULK1 Axis
inferredcites →https://doi.org/10.3390/cells7120274openalex-snapshot
The Role of Mitochondria in Reactive Oxygen Species Generation and Its Implications for Neurodegenerative Diseases
inferredcites →https://doi.org/10.4161/auto.21857openalex-snapshot
MAPK15/ERK8 stimulates autophagy by interacting with LC3 and GABARAP proteins

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4631277openalex-extracted
The HIF-1/ BNIP3 Pathway Mediates Mitophagy to Inhibit the Pyroptosis of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1002/1873-3468.14521openalex-snapshot
Cellular and physiological roles of the conserved atypical MAP kinase ERK7
inferred← citeshttps://doi.org/10.1002/advs.202509838openalex-snapshot
Energy Deficiency‐Induced ATG4B Nuclear Translocation Inhibits PRMT1‐Mediated DNA Repair and Promotes Leukemia Progression
inferred← citeshttps://doi.org/10.1002/ptr.70131openalex-snapshot
Pharmacological Regulation of Mitophagy by Natural Plant Products as a Therapeutic Target for Alzheimer's Disease
inferred← citeshttps://doi.org/10.1007/s00018-025-05639-3openalex-snapshot
Estrogen-induced circFAM171A1 regulates sheep myoblast proliferation through the oar-miR-485-5p/MAPK15/MAPK pathway
inferred← citeshttps://doi.org/10.1007/s10753-026-02514-6openalex-snapshot
MAPK15 Attenuates Intestinal Epithelial Cell Senescence-Like Phenotype to Regulate Gut Homeostasis and Inflammation by Phosphorylating Suz12 to Suppress Drp1-Mediated Mitochondrial Fission Damage
inferred← citeshttps://doi.org/10.1007/s44462-025-00012-wopenalex-snapshot
Cold-pressed flaxseed oil alleviates H2O2-induced oxidative stress in HepG2 cells by regulating the expression of the genes related to mTOR and MAPK signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bbrc.2023.149463openalex-snapshot
Prophylactic vitamin C supplementation regulates DNA demethylation to protect against cisplatin-induced acute kidney injury in mice
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115739openalex-snapshot
Regeneration and anti-inflammatory effects of stem cells and their extracellular vesicles in gynecological diseases
inferred← citeshttps://doi.org/10.1016/j.bios.2023.115588openalex-snapshot
Highly-sensitive and homogenous detection of 8-oxoguanine based DNA oxidative damage by a CRISPR-enhanced structure-switching aptamer assay
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113381openalex-snapshot
Autophagy-mediated control of ribosome homeostasis in oncogene-induced senescence
inferred← citeshttps://doi.org/10.1016/j.drudis.2025.104565openalex-snapshot
Decoding protein kinases in autophagy with small-molecule modulators for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.137032openalex-snapshot
Exploring the fascinating interplay of epigenetically modified DNA bases with two dimensional bare and P-doped Si2BN and BN sheets for biosensing applications: A compelling DFT perspective
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.111378openalex-snapshot
The HIF-1/ BNIP3 pathway mediates mitophagy to inhibit the pyroptosis of fibroblast-like synoviocytes in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1016/j.physbeh.2023.114077openalex-snapshot
Theaflavin-3,3′-digallate ameliorates learning and memory impairments in mice with premature brain aging induced by D-galactose
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103131openalex-snapshot
MAPK15 controls cellular responses to oxidative stress by regulating NRF2 activity and expression of its downstream target genes
inferred← citeshttps://doi.org/10.1016/j.talanta.2024.126002openalex-snapshot
Design of a prodrug photocage for cancer cells detection and anticancer drug release
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2024.02.004openalex-snapshot
SIRT2 regulates apoptosis by inducing mitophagy in sheep cumulus cells
inferred← citeshttps://doi.org/10.1038/s41598-025-86867-2openalex-snapshot
PLK3 weakens antioxidant defense and inhibits proliferation of porcine Leydig cells under oxidative stress
inferred← citeshttps://doi.org/10.1038/s42003-025-07482-5openalex-snapshot
Chloride intracellular channel CLIC3 mediates fibroblast cellular senescence by interacting with ERK7
inferred← citeshttps://doi.org/10.1039/d5fo02007gopenalex-snapshot
Neomangiferin prolongs the lifespan of Caenorhabditis elegans by regulating autophagy-dependent IIS and MAPK pathways via bas-1
inferred← citeshttps://doi.org/10.1042/cs20240717openalex-snapshot
To target cellular senescence in diabetic kidney disease: the known and the unknown
inferred← citeshttps://doi.org/10.1080/27694127.2022.2113016openalex-snapshot
MAPK15 controls mitochondrial fitness and contributes to prevent cellular senescence
inferred← citeshttps://doi.org/10.1093/geronb/gbaf197openalex-snapshot
Improving our understanding of the biology of aging: findings from the Age-It Research Program
inferred← citeshttps://doi.org/10.1097/hc9.0000000000000870openalex-snapshot
MAPK15 controls intracellular lipid uptake and protects mammalian liver from steatotic disease
inferred← citeshttps://doi.org/10.1111/acel.70492openalex-snapshot
From “Passive Supplementation” to “Active Repair”: Melatonin Reshapes the Treatment Paradigm for Late‐Onset Hypogonadism by Targeting Leydig Cell Senescence
inferred← citeshttps://doi.org/10.1111/cns.14819openalex-snapshot
P7C3 suppresses astrocytic senescence to protect dopaminergic neurons: Implication in the mouse model of Parkinson’s disease
inferred← citeshttps://doi.org/10.1152/ajplung.00362.2023openalex-snapshot
Revisiting airway epithelial dysfunction and mechanisms in chronic obstructive pulmonary disease: the role of mitochondrial damage
inferred← citeshttps://doi.org/10.1186/s40779-024-00536-5openalex-snapshot
Mitochondrial quality control in human health and disease
inferred← citeshttps://doi.org/10.1242/jcs.261447openalex-snapshot
Atypical MAP kinases – new insights and directions from amoeba
inferred← citeshttps://doi.org/10.26599/fshw.2024.9250093openalex-snapshot
Unsaponifiable matter from walnut oil ameliorate memory deficits and mitochondrial dysfunction in aging mice via activating Nrf2 signaling pathway
inferred← citeshttps://doi.org/10.3389/fmars.2022.1005401openalex-snapshot
Genome-wide identification of the MAPK gene family in turbot and its involvement in abiotic and biotic stress responses
inferred← citeshttps://doi.org/10.3389/fphar.2025.1725842openalex-snapshot
Pharmacological potential of Chinese botanical drugs in managing chronic kidney disease by targeting mitochondrial quality control
inferred← citeshttps://doi.org/10.3389/fphar.2026.1809770openalex-snapshot
Mitigating mitochondrial dysfunction: a novel strategy for Chinese botanical drugs against osteoporosis
inferred← citeshttps://doi.org/10.3390/ijms26115148openalex-snapshot
MAPK15 Prevents IFNB1 Expression by Suppressing Oxidative Stress-Dependent Activation of the JNK-JUN Pathway
inferred← citeshttps://doi.org/10.3390/pharmaceutics14071313openalex-snapshot
Assessing Drug-Induced Mitochondrial Toxicity in Cardiomyocytes: Implications for Preclinical Cardiac Safety Evaluation
inferred← citeshttps://doi.org/10.34133/research.0068openalex-snapshot
Natural Morin-Based Metal Organic Framework Nanoenzymes Modulate Articular Cavity Microenvironment to Alleviate Osteoarthritis
inferred← citeshttps://doi.org/10.37349/emed.2023.00180openalex-snapshot
Roles of poly(ADP-ribose) polymerase 1 and mitophagy in progeroid syndromes as well as physiological ageing
inferred← citeshttps://doi.org/10.52243/bptjm.v4i2.71openalex-snapshot
Exploring the Role of Senescent Cells in Neurodegenerative Pathology: A Window Into Promising Therapeutic Avenues
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