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ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS

https://doi.org/10.1073/pnas.0913860107
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What this work says

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

inferredcites →https://doi.org/10.1016/j.bbrc.2008.01.077openalex-snapshot
Tuberous sclerosis complex 2 loss-of-function mutation regulates reactive oxygen species production through Rac1 activation
inferredcites →https://doi.org/10.1016/j.ceb.2005.01.006openalex-snapshot
New roles for the LKB1→AMPK pathway
inferredcites →https://doi.org/10.1016/j.cell.2006.01.016openalex-snapshot
TOR Signaling in Growth and Metabolism
inferredcites →https://doi.org/10.1016/j.cell.2008.06.028openalex-snapshot
p53 Target Genes Sestrin1 and Sestrin2 Connect Genotoxic Stress and mTOR Signaling
inferredcites →https://doi.org/10.1016/j.cmet.2006.10.002openalex-snapshot
ATM-dependent suppression of stress signaling reduces vascular disease in metabolic syndrome
inferredcites →https://doi.org/10.1016/j.molcel.2004.08.025openalex-snapshot
Degradation of Misfolded Proteins Prevents ER-Derived Oxidative Stress and Cell Death
inferredcites →https://doi.org/10.1016/j.molcel.2007.03.016openalex-snapshot
Hydrogen Peroxide Sensing and Signaling
inferredcites →https://doi.org/10.1016/j.molcel.2007.12.023openalex-snapshot
Loss of the Tuberous Sclerosis Complex Tumor Suppressors Triggers the Unfolded Protein Response to Regulate Insulin Signaling and Apoptosis
inferredcites →https://doi.org/10.1016/j.molcel.2008.03.003openalex-snapshot
AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint
inferredcites →https://doi.org/10.1016/j.tibs.2005.11.009openalex-snapshot
Chutes and Ladders: the search for protein kinases that act on AMPK
inferredcites →https://doi.org/10.1016/s0092-8674(00)80086-0openalex-snapshot
Atm-Deficient Mice: A Paradigm of Ataxia Telangiectasia
inferredcites →https://doi.org/10.1016/s0092-8674(03)00929-2openalex-snapshot
TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
inferredcites →https://doi.org/10.1016/s1568-7864(01)00007-6openalex-snapshot
ATM deficiency and oxidative stress: a new dimension of defective response to DNA damage
inferredcites →https://doi.org/10.1038/35043058openalex-snapshot
The many substrates and functions of ATM
inferredcites →https://doi.org/10.1038/nature03097openalex-snapshot
Cell-cycle checkpoints and cancer
inferredcites →https://doi.org/10.1038/ng1494openalex-snapshot
Dysregulation of the TSC-mTOR pathway in human disease
inferredcites →https://doi.org/10.1038/nrn2038openalex-snapshot
Microglia-mediated neurotoxicity: uncovering the molecular mechanisms
inferredcites →https://doi.org/10.1038/sj.onc.1203622openalex-snapshot
DNA-damaging agents cause inactivation of translational regulators linked to mTOR signalling
inferredcites →https://doi.org/10.1042/0264-6021:3620481openalex-snapshot
Identification and characterization of four novel phosphorylation sites (Ser31, Ser325, Thr336 and Thr366) on LKB1/STK11, the protein kinase mutated in Peutz‒Jeghers cancer syndrome
inferredcites →https://doi.org/10.1042/bj20021284openalex-snapshot
Ionizing radiation induces ataxia telangiectasia mutated kinase (ATM)-mediated phosphorylation of LKB1/STK11 at Thr-366
inferredcites →https://doi.org/10.1056/nejmra055323openalex-snapshot
The Tuberous Sclerosis Complex
inferredcites →https://doi.org/10.1073/pnas.0502857102openalex-snapshot
The coordinate regulation of the p53 and mTOR pathways in cells
inferredcites →https://doi.org/10.1074/jbc.m511178200openalex-snapshot
Activation of Protein Kinase Cζ by Peroxynitrite Regulates LKB1-dependent AMP-activated Protein Kinase in Cultured Endothelial Cells
inferredcites →https://doi.org/10.1083/jcb.200507119openalex-snapshot
Activity of TSC2 is inhibited by AKT-mediated phosphorylation and membrane partitioning
inferredcites →https://doi.org/10.1093/embo-reports/kvf094openalex-snapshot
ROS, stress‐activated kinases and stress signaling in cancer
inferredcites →https://doi.org/10.1093/emboj/19.21.5720openalex-snapshot
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing
inferredcites →https://doi.org/10.1093/jn/137.1.229sopenalex-snapshot
Antioxidants Suppress Lymphoma and Increase Longevity in Atm-Deficient Mice ,3
inferredcites →https://doi.org/10.1126/science.1099993openalex-snapshot
Autophagy in Health and Disease: A Double-Edged Sword
inferredcites →https://doi.org/10.1126/science.1140321openalex-snapshot
ATM and ATR Substrate Analysis Reveals Extensive Protein Networks Responsive to DNA Damage
inferredcites →https://doi.org/10.1126/science.274.5293.1664openalex-snapshot
Cell Cycle Checkpoints: Preventing an Identity Crisis
inferredcites →https://doi.org/10.1126/science.7997877openalex-snapshot
Cell Cycle Control and Cancer
inferredcites →https://doi.org/10.1126/stke.4042007pe51openalex-snapshot
Dialogue Between LKB1 and AMPK: A Hot Topic at the Cellular Pole
inferredcites →https://doi.org/10.1146/annurev.biochem.75.103004.142702openalex-snapshot
LKB1-Dependent Signaling Pathways
inferredcites →https://doi.org/10.1158/0008-5472.can-04-0442openalex-snapshot
Effect of N -Acetyl Cysteine on Oxidative DNA Damage and the Frequency of DNA Deletions in Atm -Deficient Mice
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1394openalex-snapshot
Platelet-Derived Growth Factor–Induced p42/44 Mitogen-Activated Protein Kinase Activation and Cellular Growth Is Mediated by Reactive Oxygen Species in the Absence of TSC2/Tuberin
inferredcites →https://doi.org/10.1158/0008-5472.can-06-4149openalex-snapshot
The Regulation of AMPK β1, TSC2, and PTEN Expression by p53: Stress, Cell and Tissue Specificity, and the Role of These Gene Products in Modulating the IGF-1-AKT-mTOR Pathways
inferredcites →https://doi.org/10.1158/0008-5472.can-07-5756openalex-snapshot
AMP-Activated Protein Kinase Signaling Results in Cytoplasmic Sequestration of p27
inferredcites →https://doi.org/10.1158/1078-0432.ccr-08-0170openalex-snapshot
Cytoplasmic Sequestration of p27 via AKT Phosphorylation in Renal Cell Carcinoma
inferredcites →https://doi.org/10.1159/000373980openalex-snapshot
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
inferredcites →https://doi.org/10.1159/000479571openalex-snapshot
Induction of the Vitamin D Receptor Attenuates Autophagy Dysfunction-Mediated Cell Death Following Traumatic Brain Injury
inferredcites →https://doi.org/10.1172/jci13505openalex-snapshot
Role of AMP-activated protein kinase in mechanism of metformin action
inferredcites →https://doi.org/10.1172/jci17222openalex-snapshot
Loss of Tsc1/Tsc2 activates mTOR and disrupts PI3K-Akt signaling through downregulation of PDGFR
inferredcites →https://doi.org/10.1242/jcs.01540openalex-snapshot
The AMP-activated protein kinase pathway – new players upstream and downstream
inferredcites →https://doi.org/10.1371/journal.pone.0002009openalex-snapshot
Etoposide Induces ATM-Dependent Mitochondrial Biogenesis through AMPK Activation

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112901zenodo-depositor-declared
Nerolidol inhibits proliferation of leiomyoma cells via reactive oxygen species-induced DNA damage and downregulation of the ATM/Akt pathway
inferred← citeshttps://doi.org/10.1002/adbi.201800259openalex-snapshot
Crosstalk between Autophagy and Nanomaterials: Internalization, Activation, Termination
inferred← citeshttps://doi.org/10.1002/advs.202413990openalex-snapshot
Targeting TTK Inhibits Tumorigenesis of T‐Cell Lymphoma Through Dephosphorylating p38α and Activating AMPK/mTOR Pathway
inferred← citeshttps://doi.org/10.1002/bies.201600268openalex-snapshot
mTORC1 senses stresses: Coupling stress to proteostasis
inferred← citeshttps://doi.org/10.1002/cbf.3385openalex-snapshot
Multifaceted roles of ATM in autophagy: From nonselective autophagy to selective autophagy
inferred← citeshttps://doi.org/10.1002/cbic.202100641openalex-snapshot
Oxidative Stress in Cancer Therapy: Friend or Enemy?
inferred← citeshttps://doi.org/10.1002/dvdy.24522openalex-snapshot
Neurodegeneration in ataxia‐telangiectasia: Multiple roles of ATM kinase in cellular homeostasis
inferred← citeshttps://doi.org/10.1002/emmm.201000097openalex-snapshot
Stressin' Sestrins take an aging fight
inferred← citeshttps://doi.org/10.1002/ijc.29113openalex-snapshot
Sorafenib synergizes with metformin in NSCLC through AMPK pathway activation
inferred← citeshttps://doi.org/10.1002/ijc.29990openalex-snapshot
Stress management by autophagy: Implications for chemoresistance
inferred← citeshttps://doi.org/10.1002/jat.1787openalex-snapshot
Autophagy in toxicology: self‐consumption in times of stress and plenty
inferred← citeshttps://doi.org/10.1002/jcb.26217openalex-snapshot
Multiple Functions of Long Non‐Coding RNAs in Oxidative Stress, DNA Damage Response and Cancer Progression
inferred← citeshttps://doi.org/10.1002/jcb.26699openalex-snapshot
ATM and p53 combined analysis predicts survival in glioblastoma multiforme patients: A clinicopathologic study
inferred← citeshttps://doi.org/10.1002/jcb.27617openalex-snapshot
The crosstalk between trace elements with DNA damage response, repair, and oxidative stress in cancer
inferred← citeshttps://doi.org/10.1002/jcp.27979openalex-snapshot
Rapamycin enhances growth inhibition on urothelial carcinoma cells through LKB1 deficiency‐mediated mitochondrial dysregulation
inferred← citeshttps://doi.org/10.1002/jcp.30468openalex-snapshot
Oxidative stress in oocyte aging and female reproduction
inferred← citeshttps://doi.org/10.1002/jsfa.13171openalex-snapshot
Maternal folic acid and vitamin B12 supplementation during medium to late gestation promotes fetal development via improving placental antioxidant capacity, angiogenesis and amino acid transport
inferred← citeshttps://doi.org/10.1002/mabi.201600306openalex-snapshot
Exploring the Biocompatibility of Zwitterionic Copolymers for Controlling Macrophage Phagocytosis of Bacteria
inferred← citeshttps://doi.org/10.1002/path.5097openalex-snapshot
Integrating the DNA damage and protein stress responses during cancer development and treatment
inferred← citeshttps://doi.org/10.1002/wrna.1212openalex-snapshot
Translational reprogramming in cellular stress response
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_10openalex-snapshot
Other Major Types of Signaling Mediators
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_11openalex-snapshot
Signaling Pathways
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_12openalex-snapshot
Conclusion
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_2openalex-snapshot
Signaling Lipids
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_3openalex-snapshot
Preamble to Cytoplasmic Protein Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_4openalex-snapshot
Cytoplasmic Protein Tyrosine Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_5openalex-snapshot
Cytoplasmic Protein Serine/Threonine Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_6openalex-snapshot
Mitogen-Activated Protein Kinase Module
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_7openalex-snapshot
Dual-Specificity Protein Kinases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_8openalex-snapshot
Cytosolic Protein Phosphatases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4370-4_9openalex-snapshot
Guanosine Triphosphatases and Their Regulators
inferred← citeshttps://doi.org/10.1007/978-1-4614-8220-8_13openalex-snapshot
Autophagy in Necrosis: A Force for Survival
inferred← citeshttps://doi.org/10.1007/978-1-4614-8220-8_9openalex-snapshot
PARP Activation and Necrotic Cell Death
inferred← citeshttps://doi.org/10.1007/978-3-030-58532-7_16openalex-snapshot
Cell Proliferation, Survival, Necrosis and Apoptosis
inferred← citeshttps://doi.org/10.1007/978-3-030-74180-8_4openalex-snapshot
Amino Acids in Autophagy: Regulation and Function
inferred← citeshttps://doi.org/10.1007/978-3-031-55163-5_3openalex-snapshot
Mechanisms of DNA Damage Response in Mammalian Oocytes
inferred← citeshttps://doi.org/10.1007/978-3-319-06062-0_8openalex-snapshot
How to Personalize Chemotherapy in Stage IV NSCLC?
inferred← citeshttps://doi.org/10.1007/978-3-319-30079-5_3openalex-snapshot
The Complex Crosstalk Between Autophagy and ROS Signalling Pathways
inferred← citeshttps://doi.org/10.1007/978-3-319-56017-5_4openalex-snapshot
Xeroderma Pigmentosa Group A (XPA), Nucleotide Excision Repair and Regulation by ATR in Response to Ultraviolet Irradiation
inferred← citeshttps://doi.org/10.1007/978-94-007-6214-5_16openalex-snapshot
Rapamycin: Current and Future Uses
inferred← citeshttps://doi.org/10.1007/978-981-15-6930-2_3openalex-snapshot
Cross-Talk Between DNA Damage and Autophagy and Its Implication in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/978-981-99-7342-2_2openalex-snapshot
ROS and Redox Regulation/Signaling and Metabolism in Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-981-99-7342-2_4openalex-snapshot
ROS/Redox Signaling and Apoptosis/Necroptosis/Autophagy in Cancer
inferred← citeshttps://doi.org/10.1007/s00018-011-0683-9openalex-snapshot
ATM protein kinase: the linchpin of cellular defenses to stress
inferred← citeshttps://doi.org/10.1007/s00018-014-1666-4openalex-snapshot
Functional interplay between ATM/ATR-mediated DNA damage response and DNA repair pathways in oxidative stress
inferred← citeshttps://doi.org/10.1007/s00018-020-03667-9openalex-snapshot
Selective autophagy as a therapeutic target for neurological diseases
inferred← citeshttps://doi.org/10.1007/s00018-022-04625-3openalex-snapshot
New human ATM variants are able to regain ATM functions in ataxia telangiectasia disease
inferred← citeshttps://doi.org/10.1007/s00204-018-2304-yopenalex-snapshot
Arsenic induces autophagy in developmental mouse cerebral cortex and hippocampus by inhibiting PI3K/Akt/mTOR signaling pathway: involvement of blood–brain barrier’s tight junction proteins
inferred← citeshttps://doi.org/10.1007/s00418-018-1724-3openalex-snapshot
Pexophagy in yeast and mammals: an update on mysteries
inferred← citeshttps://doi.org/10.1007/s00432-012-1308-xopenalex-snapshot
Significant correlation between LKB1 and LGR5 gene expression and the association with poor recurrence-free survival in rectal cancer after preoperative chemoradiotherapy
inferred← citeshttps://doi.org/10.1007/s00441-017-2599-7openalex-snapshot
Role of primary cilia in non-dividing and post-mitotic cells
inferred← citeshttps://doi.org/10.1007/s00705-013-1602-1openalex-snapshot
Deciphering the host-pathogen protein interface in chikungunya virus-mediated sickness
inferred← citeshttps://doi.org/10.1007/s10495-016-1317-3openalex-snapshot
Reduced risk of apoptosis: mechanisms of stress responses
inferred← citeshttps://doi.org/10.1007/s10495-017-1353-7openalex-snapshot
Ursolic acid-mediated changes in glycolytic pathway promote cytotoxic autophagy and apoptosis in phenotypically different breast cancer cells
inferred← citeshttps://doi.org/10.1007/s10495-017-1424-9openalex-snapshot
Induction of reactive oxygen species: an emerging approach for cancer therapy
inferred← citeshttps://doi.org/10.1007/s10555-018-9727-zopenalex-snapshot
Pro-survival autophagy and cancer cell resistance to therapy
inferred← citeshttps://doi.org/10.1007/s10557-015-6571-zopenalex-snapshot
ATM Protein Kinase Signaling, Type 2 Diabetes and Cardiovascular Disease
inferred← citeshttps://doi.org/10.1007/s11010-013-1568-zopenalex-snapshot
TAK1 activates AMPK-dependent cell death pathway in hydrogen peroxide-treated cardiomyocytes, inhibited by heat shock protein-70
inferred← citeshttps://doi.org/10.1007/s11010-013-1608-8openalex-snapshot
AMP-activated protein kinase (AMPK)/Ulk1-dependent autophagic pathway contributes to C6 ceramide-induced cytotoxic effects in cultured colorectal cancer HT-29 cells
inferred← citeshttps://doi.org/10.1007/s11010-021-04308-wopenalex-snapshot
Isoforms of autophagy-related proteins: role in glioma progression and therapy resistance
inferred← citeshttps://doi.org/10.1007/s11030-022-10579-2openalex-snapshot
In silico study reveals unconventional interactions between MDC1 of DDR and Beclin-1 of autophagy
inferred← citeshttps://doi.org/10.1007/s11105-023-01403-8openalex-snapshot
Cd-Induced Autophagy Responses in Pakchoi as Revealed by Transcriptome Analysis
inferred← citeshttps://doi.org/10.1007/s11523-011-0173-xopenalex-snapshot
Regulation of mammalian target of rapamycin complex 1 (mTORC1) by hypoxia: causes and consequences
inferred← citeshttps://doi.org/10.1007/s11596-013-1195-7openalex-snapshot
Suppression of low-dose hyper-radiosensitivity in human lung cancer cell line A549 by radiation-induced autophagy
inferred← citeshttps://doi.org/10.1007/s12017-012-8173-2openalex-snapshot
Roles of AMP-activated Protein Kinase in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/s12032-022-01900-yopenalex-snapshot
Implications of reactive oxygen species in lung cancer and exploiting it for therapeutic interventions
inferred← citeshttps://doi.org/10.1007/s12035-017-0503-9openalex-snapshot
Mitochondrial Quality Control and Disease: Insights into Ischemia-Reperfusion Injury
inferred← citeshttps://doi.org/10.1007/s12035-017-0648-6openalex-snapshot
Radiobiological Characterization of Tuberous Sclerosis: a Delay in the Nucleo-Shuttling of ATM May Be Responsible for Radiosensitivity
inferred← citeshttps://doi.org/10.1007/s12035-022-02795-6openalex-snapshot
Mitochondrial Quality and Quantity Control: Mitophagy Is a Potential Therapeutic Target for Ischemic Stroke
inferred← citeshttps://doi.org/10.1007/s12035-025-05488-yopenalex-snapshot
Protein Phosphatase 1 Regulatory Subunit 17 (PPP1R17) Regulates Cerebral Ischemia and Ischemia–Reperfusion Brain Injury by Suppressing YAP1-Mediated Mitophagy
inferred← citeshttps://doi.org/10.1007/s12263-013-0371-5openalex-snapshot
Cellular polarity in aging: role of redox regulation and nutrition
inferred← citeshttps://doi.org/10.1007/s12275-019-8475-2openalex-snapshot
Synthetic lethal interaction between oxidative stress response and DNA damage repair in the budding yeast and its application to targeted anticancer therapy
inferred← citeshttps://doi.org/10.1007/s12275-020-9520-xopenalex-snapshot
Functional interplay between the oxidative stress response and DNA damage checkpoint signaling for genome maintenance in aerobic organisms
inferred← citeshttps://doi.org/10.1007/s12311-023-01560-2openalex-snapshot
Disproportionate Expression of ATM in Cerebellar Cortex During Human Neurodevelopment
inferred← citeshttps://doi.org/10.1007/s13238-011-1021-6openalex-snapshot
LKB1 in lung cancerigenesis: a serine/threonine kinase as tumor suppressor
inferred← citeshttps://doi.org/10.1007/s13277-015-3496-xopenalex-snapshot
Autophagy and its function in radiosensitivity
inferred← citeshttps://doi.org/10.1007/s13365-013-0189-3openalex-snapshot
Immunological control of herpes simplex virus infections
inferred← citeshttps://doi.org/10.1007/s42764-019-00005-7openalex-snapshot
Crosstalk between signaling pathways and DNA damage response
inferred← citeshttps://doi.org/10.1007/s43440-024-00609-1openalex-snapshot
The role of glucagon-like peptide-1/GLP-1R and autophagy in diabetic cardiovascular disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-405528-5.00008-0openalex-snapshot
Role of the Antioxidant Melatonin in Regulating Autophagy and Mitophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-405530-8.00012-1openalex-snapshot
Molecular Mechanisms Underlying the Activation of Autophagy Pathways by Reactive Oxygen Species and their Relevance in Cancer Progression and Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-405530-8.00017-0openalex-snapshot
Cisplatin Exposure of Squamous Cell Carcinoma Cells Leads to Modulation of the Autophagic Pathway
inferred← citeshttps://doi.org/10.1016/b978-0-12-800174-5.00017-xopenalex-snapshot
Role of the Mammalian Target of Rapamycin (mTOR) Complexes in Pancreatic β-Cell Mass Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-802937-4.00017-xopenalex-snapshot
Pro-oxidative Phytoagents Induce Autophagy in Tumors
inferred← citeshttps://doi.org/10.1016/b978-0-12-805253-2.00020-1openalex-snapshot
Autophagy, Oxidative Stress, and Redox Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-805420-8.00010-xopenalex-snapshot
Regulation of the DNA Damage Response by Autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-805421-5.00003-3openalex-snapshot
Role of Poly(ADP-Ribose) in Catalyzing Starvation-Induced Autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-814253-0.00013-9openalex-snapshot
DNA-Damage-Induced Hormetic Responses
inferred← citeshttps://doi.org/10.1016/b978-0-444-63749-9.00003-7openalex-snapshot
Plant-Derived Prooxidants as Potential Anticancer Therapeutics
inferred← citeshttps://doi.org/10.1016/j.ajpath.2011.02.022openalex-snapshot
RETRACTED: Aberrant CD8+ T-Cell Responses and Memory Differentiation upon Viral Infection of an Ataxia-Telangiectasia Mouse Model Driven by Hyper-Activated Akt and mTORC1 Signaling
inferred← citeshttps://doi.org/10.1016/j.ajpath.2016.05.001openalex-snapshot
Huntington Disease
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.06.005openalex-snapshot
Disturbed Yin–Yang balance: stress increases the susceptibility to primary and recurrent infections of herpes simplex virus type 1
inferred← citeshttps://doi.org/10.1016/j.arr.2016.05.002openalex-snapshot
Ataxia-telangiectasia (A-T): An emerging dimension of premature ageing
inferred← citeshttps://doi.org/10.1016/j.arr.2017.03.006openalex-snapshot
DNA damage response and autophagy in the degeneration of retinal pigment epithelial cells—Implications for age-related macular degeneration (AMD)
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101237openalex-snapshot
Pleiotropic effects of alpha-ketoglutarate as a potential anti-ageing agent
inferred← citeshttps://doi.org/10.1016/j.arr.2022.101653openalex-snapshot
The hallmarks of aging in Ataxia-Telangiectasia
inferred← citeshttps://doi.org/10.1016/j.arr.2024.102428openalex-snapshot
Autophagy in aging-related diseases and cancer: Principles, regulatory mechanisms and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.05.353openalex-snapshot
Mitochondrial EF4 links respiratory dysfunction and cytoplasmic translation in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.12.002openalex-snapshot
Polyethylenimine architecture-dependent metabolic imprints and perturbation of cellular redox homeostasis
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.04.003openalex-snapshot
Induction of ATM/ATR pathway combined with Vγ2Vδ2 T cells enhances cytotoxicity of ovarian cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.06.012openalex-snapshot
AMPK-α1 functions downstream of oxidative stress to mediate neuronal atrophy in Huntington's disease
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.11.010openalex-snapshot
Vascular mTOR-dependent mechanisms linking the control of aging to Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2014.11.002openalex-snapshot
Stress-mediated translational control in cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.06.001openalex-snapshot
Crosstalk between apoptosis, necrosis and autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2016.09.015openalex-snapshot
Inhibition of autophagy sensitises cells to hydrogen peroxide-induced apoptosis: Protective effect of mild thermotolerance acquired at 40 °C
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2018.06.011openalex-snapshot
mTORC1 pathway in DNA damage response
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119041openalex-snapshot
Interactions between reactive oxygen species and autophagy
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.05.090openalex-snapshot
Belinostat-induced apoptosis and growth inhibition in pancreatic cancer cells involve activation of TAK1-AMPK signaling axis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.01.117openalex-snapshot
Diversity of amino acid signaling pathways on autophagy regulation: A novel pathway for arginine
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.11.016openalex-snapshot
Activation of mTORC1 under nutrient starvation conditions increases cellular radiosensitivity in human liver cancer cell lines, HepG2 and HuH6
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.12.141openalex-snapshot
Knockdown of AMPKα decreases ATM expression and increases radiosensitivity under hypoxia and nutrient starvation in an SV40-transformed human fibroblast cell line, LM217
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.08.125openalex-snapshot
TMP21 regulates autophagy by modulating ROS production and mTOR activation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2023.149243openalex-snapshot
Oxidized ATM governs stemness of breast cancer stem cell through regulating ubiquitylation and acetylation switch
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150422openalex-snapshot
ATM facilitates autophagy and protects against oxidative stress and apoptosis in response to ER stress in vitro
inferred← citeshttps://doi.org/10.1016/j.bcp.2010.12.011openalex-snapshot
Autophagy inhibition enhances apoptosis triggered by BO-1051, an N-mustard derivative, and involves the ATM signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.12.029openalex-snapshot
Role of autophagy in chemoresistance: Regulation of the ATM-mediated DNA-damage signaling pathway through activation of DNA–PKcs and PARP-1
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.07.022openalex-snapshot
Redox modulation of the DNA damage response
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.05.007openalex-snapshot
Role of AMPK activation in oxidative cell damage: Implications for alcohol-induced liver disease
inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116729openalex-snapshot
The complex interplay between redox dysregulation and mTOR signaling pathway in cancer: A rationale for cancer treatment
inferred← citeshttps://doi.org/10.1016/j.biochi.2016.01.002openalex-snapshot
Taurine protects against As2O3-induced autophagy in pancreas of rat offsprings through Nrf2/Trx pathway
inferred← citeshttps://doi.org/10.1016/j.bj.2015.10.002openalex-snapshot
Metabolic, autophagic, and mitophagic activities in cancer initiation and progression
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.12.004openalex-snapshot
New insights into the roles of ATM and DNA-PKcs in the cellular response to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.12.043openalex-snapshot
Blockade of ataxia telangiectasia mutated sensitizes hepatoma cell lines to sorafenib by interfering with Akt signaling
inferred← citeshttps://doi.org/10.1016/j.canlet.2012.08.034openalex-snapshot
ATM and LKB1 dependent activation of AMPK sensitizes cancer cells to etoposide-induced apoptosis
inferred← citeshttps://doi.org/10.1016/j.canlet.2014.07.028openalex-snapshot
The role of oxidized ATM in the regulation of oxidative stress-induced energy metabolism reprogramming of CAFs
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.01.061openalex-snapshot
Non-apoptotic cell death in malignant tumor cells and natural compounds
inferred← citeshttps://doi.org/10.1016/j.canlet.2018.04.034openalex-snapshot
Autophagy in glioma cells: An identity crisis with a clinical perspective
inferred← citeshttps://doi.org/10.1016/j.cbi.2014.04.017openalex-snapshot
Ursolic acid induces autophagy in U87MG cells via ROS-dependent endoplasmic reticulum stress
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109149openalex-snapshot
Advanced nano drug delivery systems for neuroprotection against ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.ccr.2013.02.024openalex-snapshot
SIRT4 Has Tumor-Suppressive Activity and Regulates the Cellular Metabolic Response to DNA Damage by Inhibiting Mitochondrial Glutamine Metabolism
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.02.017openalex-snapshot
The peroxisome as a cell signaling organelle
inferred← citeshttps://doi.org/10.1016/j.cell.2013.07.031openalex-snapshot
Inhibition of mTORC1 by Astrin and Stress Granules Prevents Apoptosis in Cancer Cells
inferred← citeshttps://doi.org/10.1016/j.cellsig.2012.01.008openalex-snapshot
Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling
inferred← citeshttps://doi.org/10.1016/j.cellsig.2012.09.020openalex-snapshot
Starvation-induced autophagy is regulated by mitochondrial reactive oxygen species leading to AMPK activation
inferred← citeshttps://doi.org/10.1016/j.cellsig.2013.08.010openalex-snapshot
ATM pathway is essential for ionizing radiation-induced autophagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110354openalex-snapshot
K48/K63-linked polyubiquitination of ATG9A by TRAF6 E3 ligase regulates oxidative stress-induced autophagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113402openalex-snapshot
ATM-CHK2-TRIM32 axis regulates ATG7 ubiquitination to initiate autophagy under oxidative stress
inferred← citeshttps://doi.org/10.1016/j.clim.2011.03.007openalex-snapshot
Premature ageing of the immune system underlies immunodeficiency in ataxia telangiectasia
inferred← citeshttps://doi.org/10.1016/j.clim.2016.11.015openalex-snapshot
Abnormal cell-clearance and accumulation of autophagic vesicles in lymphocytes from patients affected with Ataxia-Teleangiectasia
inferred← citeshttps://doi.org/10.1016/j.clim.2019.07.003openalex-snapshot
Metabolic reprogramming in memory CD4 T cell responses of old adults
inferred← citeshttps://doi.org/10.1016/j.cmet.2012.06.003openalex-snapshot
Wip1-Dependent Regulation of Autophagy, Obesity, and Atherosclerosis
inferred← citeshttps://doi.org/10.1016/j.cotox.2017.10.006openalex-snapshot
Reciprocity in ROS and autophagic signaling
inferred← citeshttps://doi.org/10.1016/j.dci.2023.105128openalex-snapshot
PyLKB1 regulates glucose transport via activating PyAMPKα in Yesso Scallop Patinopecten yessoensis under high temperature stress
inferred← citeshttps://doi.org/10.1016/j.dld.2022.01.131openalex-snapshot
Possible role of nuclear factor erythroid 2–related factor 2 in the progression of human colon precancerous lesions
inferred← citeshttps://doi.org/10.1016/j.dnarep.2011.05.004openalex-snapshot
ATM protects against oxidative stress induced by oxidized low-density lipoprotein
inferred← citeshttps://doi.org/10.1016/j.dnarep.2013.04.014openalex-snapshot
The appropriateness of the mouse model for ataxia-telangiectasia: Neurological defects but no neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.dnarep.2013.11.002openalex-snapshot
Intrinsic mitochondrial DNA repair defects in Ataxia Telangiectasia
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.12.009openalex-snapshot
ATM kinase: Much more than a DNA damage responsive protein
inferred← citeshttps://doi.org/10.1016/j.dnarep.2020.102950openalex-snapshot
The cerebellar degeneration in ataxia-telangiectasia: A case for genome instability
inferred← citeshttps://doi.org/10.1016/j.dnarep.2021.103155openalex-snapshot
DNA damage and regulation of protein homeostasis
inferred← citeshttps://doi.org/10.1016/j.ejcb.2016.10.005openalex-snapshot
Autophagy and the invisible line between life and death
inferred← citeshttps://doi.org/10.1016/j.ejcb.2018.09.004openalex-snapshot
Redox cell signaling and hepatic progenitor cells
inferred← citeshttps://doi.org/10.1016/j.ejcb.2026.151540openalex-snapshot
MDC1 promotes nuclear localization of Beclin-1 and supports its role in ATM pathway in response to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174562openalex-snapshot
PPAR-gamma agonists: Potential modulators of autophagy in obesity
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120574openalex-snapshot
The activated ATM/AMPK/mTOR axis promotes autophagy in response to oxidative stress-mediated DNA damage co-induced by molybdenum and cadmium in duck testes
inferred← citeshttps://doi.org/10.1016/j.etp.2014.01.004openalex-snapshot
Autophagy in arsenic carcinogenesis
inferred← citeshttps://doi.org/10.1016/j.exphem.2011.08.009openalex-snapshot
The aging effect of chemotherapy on cultured human mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.fct.2014.05.006openalex-snapshot
Sodium arsenite induces ROS-dependent autophagic cell death in pancreatic β-cells
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.02.001openalex-snapshot
TSC1/TSC2 signaling in the CNS
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.03.010openalex-snapshot
The role of LKB1 and AMPK in cellular responses to stress and damage
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.05.013openalex-snapshot
Beyond ATM: The protein kinase landscape of the DNA damage response
inferred← citeshttps://doi.org/10.1016/j.fmre.2023.04.016openalex-snapshot
Peroxisome and pexophagy in neurological diseases
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.09.006openalex-snapshot
Oxidative stress, inflammation, and cancer: How are they linked?
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.07.011openalex-snapshot
Reactive oxygen species regulation of autophagy in cancer: Implications for cancer treatment
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.07.013openalex-snapshot
Deconvoluting the role of reactive oxygen species and autophagy in human diseases
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.03.025openalex-snapshot
Redox regulation of antioxidants, autophagy, and the response to stress: Implications for electrophile therapeutics
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.01.004openalex-snapshot
Reactive oxygen species and cancer paradox: To promote or to suppress?
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.09.008openalex-snapshot
Pharmacologic ascorbate induces neuroblastoma cell death by hydrogen peroxide mediated DNA damage and reduction in cancer cell glycolysis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.02.047openalex-snapshot
AMP-activated protein kinase: A remarkable contributor to preserve a healthy heart against ROS injury
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.01.024openalex-snapshot
Both selenium deficiency and excess impair male reproductive system via inducing oxidative stress-activated PI3K/AKT-mediated apoptosis and cell proliferation signaling in testis of mice
inferred← citeshttps://doi.org/10.1016/j.gendis.2014.06.002openalex-snapshot
LKB1 tumor suppressor: Therapeutic opportunities knock when LKB1 is inactivated
inferred← citeshttps://doi.org/10.1016/j.heliyon.2016.e00083openalex-snapshot
Chloroquine increases phosphorylation of AMPK and Akt in myotubes
inferred← citeshttps://doi.org/10.1016/j.heliyon.2022.e09957openalex-snapshot
What we have learnt from Drosophila model organism: the coordination between insulin signaling pathway and tumor cells
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e38959openalex-snapshot
The role of autophagy in brain health and disease: Insights into exosome and autophagy interactions
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2020.09.096openalex-snapshot
Thiol antioxidant thioredoxin reductase: A prospective biochemical crossroads between anticancer and antiparasitic treatments of the modern era
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2012.01.026openalex-snapshot
Chloroquine Improves Survival and Hematopoietic Recovery After Lethal Low-Dose-Rate Radiation
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2019.10.045openalex-snapshot
Human CCR6+ Th17 Lymphocytes Are Highly Sensitive to Radiation-Induced Senescence and Are a Potential Target for Prevention of Radiation-Induced Toxicity
inferred← citeshttps://doi.org/10.1016/j.immuni.2013.08.039openalex-snapshot
Anthracyclines Induce DNA Damage Response-Mediated Protection against Severe Sepsis
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.110053openalex-snapshot
Forsythoside A regulates autophagy and apoptosis through the AMPK/mTOR/ULK1 pathway and alleviates inflammatory damage in MAC-T cells
inferred← citeshttps://doi.org/10.1016/j.isci.2022.105115openalex-snapshot
RPRM negatively regulates ATM levels through its nuclear translocation on irradiation mediated by CDK4/6 and IPO11
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110265openalex-snapshot
Circulating biomarkers of kidney angiomyolipoma and cysts in tuberous sclerosis complex patients
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112118openalex-snapshot
A bacterial genotoxin reveals a p53-proteasome-LC3 regulatory axis that drives the suppression of autophagy in cells experiencing sublethal DNA damage
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104570openalex-snapshot
Posttranslational regulation of liver kinase B1 in human cancer
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104906openalex-snapshot
Identification of a novel mitochondria-localized LKB1 variant required for the regulation of the oxidative stress response
inferred← citeshttps://doi.org/10.1016/j.jchromb.2020.122250openalex-snapshot
An improved pseudotargeted GC–MS/MS-based metabolomics method and its application in radiation-induced hepatic injury in a rat model
inferred← citeshttps://doi.org/10.1016/j.jff.2015.12.031openalex-snapshot
Inhibitory effect of Erinacines A on the growth of DLD-1 colorectal cancer cells is induced by generation of reactive oxygen species and activation of p70S6K and p21
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.122227openalex-snapshot
Arsenic induces dysfunctional autophagy via dual regulation of mTOR pathway and Beclin1-Vps34/PI3K complex in MLTC-1 cells
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2018.02.010openalex-snapshot
Low power lasers on genomic stability
inferred← citeshttps://doi.org/10.1016/j.jprot.2012.03.040openalex-snapshot
A two-dimensional screen for AMPK substrates identifies tumor suppressor fumarate hydratase as a preferential AMPKα2 substrate
inferred← citeshttps://doi.org/10.1016/j.lfs.2017.12.001openalex-snapshot
Diabetic retinopathy pathogenesis and the ameliorating effects of melatonin; involvement of autophagy, inflammation and oxidative stress
inferred← citeshttps://doi.org/10.1016/j.lfs.2022.120787openalex-snapshot
Transcriptional profiling reveals ataxia telangiectasia mutated pathways regulate joint copper and arsenic toxicity for hepatic metalloplasia and anti-cancer therapies
inferred← citeshttps://doi.org/10.1016/j.mad.2019.111194openalex-snapshot
The NAD+-mitophagy axis in healthy longevity and in artificial intelligence-based clinical applications
inferred← citeshttps://doi.org/10.1016/j.mad.2020.111207openalex-snapshot
Mitophagy and DNA damage signaling in human aging
inferred← citeshttps://doi.org/10.1016/j.mad.2020.111296openalex-snapshot
ATM-deficient neural precursors develop senescence phenotype with disturbances in autophagy
inferred← citeshttps://doi.org/10.1016/j.mam.2018.02.003openalex-snapshot
Redox control in cancer development and progression
inferred← citeshttps://doi.org/10.1016/j.matbio.2021.02.004openalex-snapshot
Causes and consequences of DNA damage-induced autophagy
inferred← citeshttps://doi.org/10.1016/j.mce.2012.04.009openalex-snapshot
Role of melatonin in the regulation of autophagy and mitophagy: A review
inferred← citeshttps://doi.org/10.1016/j.mcpro.2025.101035openalex-snapshot
mTORC2 Regulates Non-homologous End Joining Through Modulating the Temporal Dynamics of 53BP1
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.09.023openalex-snapshot
Autophagy and the Integrated Stress Response
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.09.028openalex-snapshot
Translational Regulation of Gene Expression during Conditions of Cell Stress
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