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Regulation of autophagy by cytoplasmic p53
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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.ccr.2006.06.001openalex-snapshot
Autophagy promotes tumor cell survival and restricts necrosis, inflammation, and tumorigenesis
inferredcites →https://doi.org/10.1016/j.ceb.2007.02.003openalex-snapshot
Hypoxia signalling controls metabolic demand
inferredcites →https://doi.org/10.1016/j.cell.2005.07.002openalex-snapshot
Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
inferredcites →https://doi.org/10.1016/j.cell.2006.05.034openalex-snapshot
DRAM, a p53-Induced Modulator of Autophagy, Is Critical for Apoptosis
inferredcites →https://doi.org/10.1016/j.cell.2006.12.007openalex-snapshot
Modeling the Therapeutic Efficacy of p53 Restoration in Tumors
inferredcites →https://doi.org/10.1016/j.cell.2006.12.044openalex-snapshot
Autophagy Gene-Dependent Clearance of Apoptotic Cells during Embryonic Development
inferredcites →https://doi.org/10.1016/j.cell.2007.12.018openalex-snapshot
Autophagy in the Pathogenesis of Disease
inferredcites →https://doi.org/10.1016/j.molcel.2005.03.027openalex-snapshot
AMP-Activated Protein Kinase Induces a p53-Dependent Metabolic Checkpoint
inferredcites →https://doi.org/10.1016/s0014-4827(02)00019-8openalex-snapshot
Regulation of tumor suppressors by nuclear-cytoplasmic shuttling
inferredcites →https://doi.org/10.1016/s0092-8674(00)81683-9openalex-snapshot
The Hallmarks of Cancer
inferredcites →https://doi.org/10.1016/s1097-2765(03)00050-9openalex-snapshot
p53 Has a Direct Apoptogenic Role at the Mitochondria
inferredcites →https://doi.org/10.1016/s1535-6108(03)00272-1openalex-snapshot
Pharmacologic activation of p53 elicits Bax-dependent apoptosis in the absence of transcription
inferredcites →https://doi.org/10.1038/45257openalex-snapshot
Induction of autophagy and inhibition of tumorigenesis by beclin 1
inferredcites →https://doi.org/10.1038/nature05529openalex-snapshot
Senescence and tumour clearance is triggered by p53 restoration in murine liver carcinomas
inferredcites →https://doi.org/10.1038/ncb1123openalex-snapshot
Mitochondrial p53 activates Bak and causes disruption of a Bak–Mcl1 complex
inferredcites →https://doi.org/10.1038/nm1146openalex-snapshot
Small molecule RITA binds to p53, blocks p53–HDM-2 interaction and activates p53 function in tumors
inferredcites →https://doi.org/10.1038/nrc1738openalex-snapshot
Lysosomes and autophagy in cell death control
inferredcites →https://doi.org/10.1038/nrc2012openalex-snapshot
Regulating the p53 pathway: in vitro hypotheses, in vivo veritas
inferredcites →https://doi.org/10.1038/nrd2062openalex-snapshot
Current development of mTOR inhibitors as anticancer agents
inferredcites →https://doi.org/10.1038/nrd2272openalex-snapshot
Potential therapeutic applications of autophagy
inferredcites →https://doi.org/10.1038/nrm1660openalex-snapshot
Autophagy in metazoans: cell survival in the land of plenty
inferredcites →https://doi.org/10.1038/nrm2239openalex-snapshot
Self-eating and self-killing: crosstalk between autophagy and apoptosis
inferredcites →https://doi.org/10.1038/sj.cdd.4402099openalex-snapshot
Regulation of autophagy by the inositol trisphosphate receptor
inferredcites →https://doi.org/10.1038/sj.emboj.7601689openalex-snapshot
Functional and physical interaction between Bcl‐XL and a BH3‐like domain in Beclin‐1
inferredcites →https://doi.org/10.1038/sj.onc.1209952openalex-snapshot
The p53 knowledgebase: an integrated information resource for p53 research
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.m507611200openalex-snapshot
WT p53, but Not Tumor-derived Mutants, Bind to Bcl2 via the DNA Binding Domain and Induce Mitochondrial Permeabilization
inferredcites →https://doi.org/10.1074/jbc.m605488200openalex-snapshot
AMP-activated Protein Kinase and the Regulation of Autophagic Proteolysis
inferredcites →https://doi.org/10.1074/jbc.m607007200openalex-snapshot
Endoplasmic Reticulum Stress Triggers Autophagy
inferredcites →https://doi.org/10.1091/mbc.e03-09-0704openalex-snapshot
In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker
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/10.1101/gad.1165804openalex-snapshot
Endoplasmic reticulum stress induces p53 cytoplasmic localization and prevents p53-dependent apoptosis by a pathway involving glycogen synthase kinase-3β
inferredcites →https://doi.org/10.1126/science.1092472openalex-snapshot
In Vivo Activation of the p53 Pathway by Small-Molecule Antagonists of MDM2
inferredcites →https://doi.org/10.1126/science.1092734openalex-snapshot
Direct Activation of Bax by p53 Mediates Mitochondrial Membrane Permeabilization and Apoptosis
inferredcites →https://doi.org/10.1126/science.2649981openalex-snapshot
Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas
inferredcites →https://doi.org/10.1126/science.285.5434.1733openalex-snapshot
A Chemical Inhibitor of p53 That Protects Mice from the Side Effects of Cancer Therapy
inferredcites →https://doi.org/10.1128/mcb.01453-06openalex-snapshot
Autophagy Is Activated for Cell Survival after Endoplasmic ReticulumStress
inferredcites →https://doi.org/10.1128/mcb.25.21.9392-9405.2005openalex-snapshot
Endoplasmic Reticulum Stress Accelerates p53 Degradation by the Cooperative Actions of Hdm2 and Glycogen Synthase Kinase 3β
inferredcites →https://doi.org/10.1128/mcb.25.3.1025-1040.2005openalex-snapshot
Inhibition of Macroautophagy Triggers Apoptosis
inferredcites →https://doi.org/10.1158/0008-5472.can-05-1084openalex-snapshot
Mitochondrially Targeted p53 Has Tumor Suppressor Activities In vivo
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/10.1172/jci26390openalex-snapshot
Autophagy in cell death: an innocent convict?
inferredcites →https://doi.org/10.1172/jci28833openalex-snapshot
Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma
inferredcites →https://doi.org/10.1172/jci6863openalex-snapshot
Disruption of p53 in human cancer cells alters the responses to therapeutic agents
inferredcites →https://doi.org/10.4161/auto.4600openalex-snapshot
How to Interpret LC3 Immunoblotting
inferredcites →https://doi.org/10.4161/auto.5338openalex-snapshot
Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5281/zenodo.59821openalex-extracted
Huhs1015 Promotes Autophagic Xiap Degradation To Induce Apoptosis Of Gastrointestinal Cancer Cells
inferred← citeshttps://doi.org/10.1002/1873-3468.70060openalex-snapshot
Decoding the dual role of autophagy in cancer through transcriptional and epigenetic regulation
inferred← citeshttps://doi.org/10.1002/1873-3468.70061openalex-snapshot
Autophagy in cancer and protein conformational disorders
inferred← citeshttps://doi.org/10.1002/1878-0261.13704openalex-snapshot
Inhibition of autophagy as a novel treatment for neurofibromatosis type 1 tumors
inferred← citeshttps://doi.org/10.1002/2211-5463.12855openalex-snapshot
PBK attenuates paclitaxel‐induced autophagic cell death by suppressing p53 in H460 non‐small‐cell lung cancer cells
inferred← citeshttps://doi.org/10.1002/2211-5463.70138openalex-snapshot
ATG4B is required for mTORC1 ‐mediated anabolic activity and is associated with clinical outcomes in non‐small cell lung cancer
inferred← citeshttps://doi.org/10.1002/9780470622728.ch5openalex-snapshot
The Interplay of Cancer and Biology
inferred← citeshttps://doi.org/10.1002/9781118148143.ch13openalex-snapshot
Oxidative Stress‐Mediated Signaling Pathways by Environmental Stressors
inferred← citeshttps://doi.org/10.1002/9781118399668.ch38openalex-snapshot
Malignant Epithelial Neoplasms of the Large Bowel
inferred← citeshttps://doi.org/10.1002/9781118677551.ch11openalex-snapshot
Helicobacter PyloriInfection Control by Autophagy
inferred← citeshttps://doi.org/10.1002/9781119423195.ch38openalex-snapshot
Malignant epithelial neoplasms of the large intestine
inferred← citeshttps://doi.org/10.1002/advs.202303336openalex-snapshot
MLF2 Negatively Regulates P53 and Promotes Colorectal Carcinogenesis
inferred← citeshttps://doi.org/10.1002/advs.202503473openalex-snapshot
Lipid Droplet‐Organized MDM2‐Mediated P53 Degradation: A Metabolic Switch Governing Diet‐Driven Tumor Progression
inferred← citeshttps://doi.org/10.1002/alz.70198openalex-snapshot
Genome‐wide association analysis identifies APOE as a mitophagy modifier in Lewy body disease
inferred← citeshttps://doi.org/10.1002/bies.201300117openalex-snapshot
How do I kill thee? Let me count the ways: p53 regulates PARP ‐1 dependent necrosis
inferred← citeshttps://doi.org/10.1002/biof.101openalex-snapshot
Role of mitochondrial ion channels in cell death
inferred← citeshttps://doi.org/10.1002/biot.70069openalex-snapshot
Effect of Apoptosis and Autophagy on Recombinant Protein Expression in Chinese Hamster Ovary Cells
inferred← citeshttps://doi.org/10.1002/cam4.5577openalex-snapshot
Autophagy: A challengeable paradox in cancer treatment
inferred← citeshttps://doi.org/10.1002/cbin.10379openalex-snapshot
Oncogenic nature of a novel mutant AATF and its interactome existing within human cancer cells
inferred← citeshttps://doi.org/10.1002/cmdc.202000522openalex-snapshot
Potency and Selectivity Optimization of Tryptophanol‐Derived Oxazoloisoindolinones: Novel p53 Activators in Human Colorectal Cancer
inferred← citeshttps://doi.org/10.1002/cncr.31978openalex-snapshot
Targeting autophagy using natural compounds for cancer prevention and therapy
inferred← citeshttps://doi.org/10.1002/eji.201242918openalex-snapshot
The NLRP 3 inflammasome affects DNA damage responses after oxidative and genotoxic stress in dendritic cells
inferred← citeshttps://doi.org/10.1002/iid3.70041openalex-snapshot
Promising and challenging phytochemicals targeting LC3 mediated autophagy signaling in cancer therapy
inferred← citeshttps://doi.org/10.1002/j.2769-2795.2018.tb00027.xopenalex-snapshot
Current status of autophagy in cerebral ischemia‐reperfusion injury
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.24465openalex-snapshot
mTOR inhibitors radiosensitize PTEN‐deficient non‐small‐cell lung cancer cells harboring an EGFR activating mutation by inducing autophagy
inferred← citeshttps://doi.org/10.1002/jcb.25474openalex-snapshot
Expression of cFLIPL Determines the Basal Interaction of Bcl‐2 With Beclin‐1 and Regulates p53 Dependent Ubiquitination of Beclin‐1 During Autophagic Stress
inferred← citeshttps://doi.org/10.1002/jcp.22210openalex-snapshot
Lipopolysaccharide induces autophagy through BIRC2 in human umbilical vein endothelial cells
inferred← citeshttps://doi.org/10.1002/jcp.22805openalex-snapshot
Distinct cellular responses induced by saporin and a transferrin–saporin conjugate in two different human glioblastoma cell lines
inferred← citeshttps://doi.org/10.1002/jcp.24420openalex-snapshot
Autophagy and senescence in cancer therapy
inferred← citeshttps://doi.org/10.1002/jcp.27354openalex-snapshot
Mutant p53R248Q downregulates oxidative phosphorylation and upregulates glycolysis under normoxia and hypoxia in human cervix cancer cells
inferred← citeshttps://doi.org/10.1002/jcp.30502openalex-snapshot
Regulation of autophagy by protein methylation and acetylation in cancer
inferred← citeshttps://doi.org/10.1002/jnr.23806openalex-snapshot
Sirtuins as modifiers of Parkinson's disease pathology
inferred← citeshttps://doi.org/10.1002/mc.23372openalex-snapshot
Autophagy awakens—the myriad roles of autophagy in head and neck cancer development and therapeutic response
inferred← citeshttps://doi.org/10.1002/med.21531openalex-snapshot
The multifaceted role of autophagy in cancer and the microenvironment
inferred← citeshttps://doi.org/10.1002/med.21662openalex-snapshot
How autophagy can restore proteostasis defects in multiple diseases?
inferred← citeshttps://doi.org/10.1002/med.21733openalex-snapshot
Autophagy and cardiac diseases: Therapeutic potential of natural products
inferred← citeshttps://doi.org/10.1002/med.22033openalex-snapshot
Antineoplastics for treating Alzheimer's disease and dementia: Evidence from preclinical and observational studies
inferred← citeshttps://doi.org/10.1002/mog2.70064openalex-snapshot
The Dual Role of Autophagy in Cancer: Mechanisms and Therapeutic Strategies
inferred← citeshttps://doi.org/10.1002/path.2637openalex-snapshot
Massively regulated genes: the example of TP53
inferred← citeshttps://doi.org/10.1002/path.4115openalex-snapshot
Fibroblast autophagy in fibrotic disorders
inferred← citeshttps://doi.org/10.1002/ptr.5196openalex-snapshot
Turmeric Toxicity in A431 Epidermoid Cancer Cells Associates with Autophagy Degradation of Anti‐apoptotic and Anti‐autophagic p53 Mutant
inferred← citeshttps://doi.org/10.1007/400_2008_25openalex-snapshot
Autophagy in Cancer and Chemotherapy
inferred← citeshttps://doi.org/10.1007/978-1-0716-1154-8_13openalex-snapshot
Investigating Conformational Dynamics and Allostery in the p53 DNA-Binding Domain Using Molecular Simulations
inferred← citeshttps://doi.org/10.1007/978-1-0716-1433-4_10openalex-snapshot
Analysis of Proapoptotic Protein Trafficking to and from Mitochondria
inferred← citeshttps://doi.org/10.1007/978-1-0716-2071-7_1openalex-snapshot
A Balance Between Autophagy and Other Cell Death Modalities in Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-9293-0_1openalex-snapshot
Molecular Pathways of Different Types of Cell Death: Many Roads to Death
inferred← citeshttps://doi.org/10.1007/978-1-4419-1075-2_10openalex-snapshot
Mining Cellular Senescence for Drug Targets
inferred← citeshttps://doi.org/10.1007/978-1-4419-1770-6_6openalex-snapshot
p53, ARF, and the Control of Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-4614-1680-7_11openalex-snapshot
Autophagy and Self-Defense
inferred← citeshttps://doi.org/10.1007/978-1-4614-3801-4_7openalex-snapshot
Neural Stem Cell Death Regulation in Nervous System Development and Disease
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_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/10.1007/978-1-4614-4599-9_11openalex-snapshot
Cell-Death Pathways and Mitochondria
inferred← citeshttps://doi.org/10.1007/978-1-4614-6561-4_11openalex-snapshot
The Cross Talk Between Apoptosis and Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-4614-6561-4_7openalex-snapshot
Oncogenes and Tumor Suppressor Genes in Autophagy
inferred← citeshttps://doi.org/10.1007/978-1-4614-6828-8_19openalex-snapshot
Autophagy and Prostate Cancer Therapeutics
inferred← citeshttps://doi.org/10.1007/978-1-4939-0268-2_30openalex-snapshot
Aging-Related Changes in Mitochondrial Function and Implication for Heart Failure Therapy
inferred← citeshttps://doi.org/10.1007/978-1-4939-1875-1_14openalex-snapshot
Analysis of Pro-apoptotic Protein Trafficking to and from Mitochondria
inferred← citeshttps://doi.org/10.1007/978-1-60327-381-7_30openalex-snapshot
Autophagy and Cell Death
inferred← citeshttps://doi.org/10.1007/978-1-61779-430-8_9openalex-snapshot
Evaluation of rapamycin-induced cell death.
inferred← citeshttps://doi.org/10.1007/978-1-61779-891-7_8openalex-snapshot
Ubiquitylation - Dependent Signaling in Heart Disease
inferred← citeshttps://doi.org/10.1007/978-1-62703-456-2_10openalex-snapshot
Modulation of Autophagy as a Novel Cancer Therapeutic Strategy
inferred← citeshttps://doi.org/10.1007/978-3-031-62036-2_1openalex-snapshot
Organelle Communication with the Nucleus
inferred← citeshttps://doi.org/10.1007/978-3-031-66421-2_11openalex-snapshot
Interplay Between Autophagy and Apoptosis in Cancer: Mechanisms and Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/978-3-319-42740-9_6openalex-snapshot
Adult and Cancer Stem Cells: Perspectives on Autophagic Fate Determinations and Molecular Intervention
inferred← citeshttps://doi.org/10.1007/978-3-319-42740-9_7openalex-snapshot
Role of Autophagy in Tumor Progression and Regression
inferred← citeshttps://doi.org/10.1007/978-3-319-51436-9_5openalex-snapshot
Tissue-Specific Functions of p53 During Kidney Development
inferred← citeshttps://doi.org/10.1007/978-3-642-00302-8_2openalex-snapshot
Macroautophagy Signaling and Regulation
inferred← citeshttps://doi.org/10.1007/978-3-7091-1431-5_5openalex-snapshot
Autophagy in Glioma Cells
inferred← citeshttps://doi.org/10.1007/978-4-431-55825-5_8openalex-snapshot
The Role of Transglutaminase Type 2 in the Regulation of Autophagy
inferred← citeshttps://doi.org/10.1007/978-94-007-6211-4_14openalex-snapshot
Autophagy, Cell Death, and Cancer
inferred← citeshttps://doi.org/10.1007/978-94-017-8984-4_12openalex-snapshot
Crosstalk Between p53 and Mitochondrial Metabolism
inferred← citeshttps://doi.org/10.1007/978-94-017-9211-0_18openalex-snapshot
The Role of Tumor Suppressor p53 in the Antioxidant Defense and Metabolism
inferred← citeshttps://doi.org/10.1007/978-981-15-1067-0_2openalex-snapshot
Metabolic Changes and Their Characterization
inferred← citeshttps://doi.org/10.1007/978-981-15-6930-2_11openalex-snapshot
The Autophagy Conundrum in Cancer Development, Progression and Therapeutics
inferred← citeshttps://doi.org/10.1007/978-981-99-7342-2_7openalex-snapshot
P53, ROS: Redox Regulation Signaling, Metabolic Reprogramming, and Autophagy in Cancer
inferred← citeshttps://doi.org/10.1007/s00005-012-0205-yopenalex-snapshot
Autophagy, Apoptosis, Mitoptosis and Necrosis: Interdependence Between Those Pathways and Effects on Cancer
inferred← citeshttps://doi.org/10.1007/s00018-010-0284-zopenalex-snapshot
Regulation of autophagy in mammals and its interplay with apoptosis
inferred← citeshttps://doi.org/10.1007/s00018-012-1032-3openalex-snapshot
Tightrope act: autophagy in stem cell renewal, differentiation, proliferation, and aging
inferred← citeshttps://doi.org/10.1007/s00018-017-2632-8openalex-snapshot
Pathogenic mutation in the ALS/FTD gene, CCNF, causes elevated Lys48-linked ubiquitylation and defective autophagy
inferred← citeshttps://doi.org/10.1007/s00018-017-2695-6openalex-snapshot
Downregulation of p53 drives autophagy during human trophoblast differentiation
inferred← citeshttps://doi.org/10.1007/s00018-019-03161-xopenalex-snapshot
Protein methylation functions as the posttranslational modification switch to regulate autophagy
inferred← citeshttps://doi.org/10.1007/s00018-020-03694-6openalex-snapshot
The regulatory roles of p53 in cardiovascular health and disease
inferred← citeshttps://doi.org/10.1007/s00109-010-0650-1openalex-snapshot
Dynamics of microRNA biogenesis: crosstalk between p53 network and microRNA processing pathway
inferred← citeshttps://doi.org/10.1007/s00109-011-0735-5openalex-snapshot
Metabolic regulation by p53
inferred← citeshttps://doi.org/10.1007/s00204-014-1448-7openalex-snapshot
The mystery of BCL2 family: Bcl-2 proteins and apoptosis: an update
inferred← citeshttps://doi.org/10.1007/s00280-013-2363-yopenalex-snapshot
Autophagy, a novel target for chemotherapeutic intervention of thyroid cancer
inferred← citeshttps://doi.org/10.1007/s00404-020-05607-1openalex-snapshot
Physiological and pathological regulation of autophagy in pregnancy
inferred← citeshttps://doi.org/10.1007/s00702-021-02431-yopenalex-snapshot
Protein clearance strategies for disease intervention
inferred← citeshttps://doi.org/10.1007/s10495-008-0303-9openalex-snapshot
Immunogenic cell death modalities and their impact on cancer treatment
inferred← citeshttps://doi.org/10.1007/s10495-008-0307-5openalex-snapshot
The paradox of autophagy and its implication in cancer etiology and therapy
inferred← citeshttps://doi.org/10.1007/s10495-011-0589-xopenalex-snapshot
Conversation between apoptosis and autophagy: “Is it your turn or mine?”
inferred← citeshttps://doi.org/10.1007/s10495-011-0685-yopenalex-snapshot
Induction of autophagy in hepatocellular carcinoma cells by SB203580 requires activation of AMPK and DAPK but not p38 MAPK
inferred← citeshttps://doi.org/10.1007/s10495-012-0790-6openalex-snapshot
Autophagy induced by p53-reactivating molecules protects pancreatic cancer cells from apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-014-0967-2openalex-snapshot
Autophagy and apoptosis: where do they meet?
inferred← citeshttps://doi.org/10.1007/s10495-016-1299-1openalex-snapshot
MG132 plus apoptosis antigen-1 (APO-1) antibody cooperate to restore p53 activity inducing autophagy and p53-dependent apoptosis in HPV16 E6-expressing keratinocytes
inferred← citeshttps://doi.org/10.1007/s10495-019-01537-9openalex-snapshot
Effects of annexin A7 inhibitor-ABO on the expression and distribution of long noncoding RNA-CERNA1 in vascular endothelial cells apoptosis
inferred← citeshttps://doi.org/10.1007/s10495-022-01734-zopenalex-snapshot
XIAP as a multifaceted molecule in Cellular Signaling
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/s10557-024-07642-5openalex-snapshot
Ferroptosis in Cardiovascular Diseases and Ferroptosis-Related Intervention Approaches
inferred← citeshttps://doi.org/10.1007/s10571-014-0116-zopenalex-snapshot
The Molecular Mechanisms Between Autophagy and Apoptosis: Potential Role in Central Nervous System Disorders
inferred← citeshttps://doi.org/10.1007/s10571-016-0452-2openalex-snapshot
Could Sirtuin Activities Modify ALS Onset and Progression?
inferred← citeshttps://doi.org/10.1007/s10741-009-9137-yopenalex-snapshot
How does the heart (not) die? The role of autophagy in cardiomyocyte homeostasis and cell death
inferred← citeshttps://doi.org/10.1007/s11010-014-2183-3openalex-snapshot
Coordinated regulation of autophagy and apoptosis determines endothelial cell fate during Dengue virus type 2 infection
inferred← citeshttps://doi.org/10.1007/s11010-016-2853-4openalex-snapshot
Akt/AMPK/mTOR pathway was involved in the autophagy induced by vitamin E succinate in human gastric cancer SGC-7901 cells
inferred← citeshttps://doi.org/10.1007/s11011-021-00839-9openalex-snapshot
The role of carbonic anhydrase III and autophagy in type 2 diabetes with cardio-cerebrovascular disease
inferred← citeshttps://doi.org/10.1007/s11033-021-06706-1openalex-snapshot
Crosslink between p53 and metastasis: focus on epithelial–mesenchymal transition, cancer stem cell, angiogenesis, autophagy, and anoikis
inferred← citeshttps://doi.org/10.1007/s11064-016-2141-4openalex-snapshot
Silibinin ameliorates Aβ25-35-induced memory deficits in rats by modulating autophagy and attenuating neuroinflammation as well as oxidative stress
inferred← citeshttps://doi.org/10.1007/s11357-011-9324-3openalex-snapshot
MiR-34 modulates Caenorhabditis elegans lifespan via repressing the autophagy gene atg9
inferred← citeshttps://doi.org/10.1007/s12010-023-04424-xopenalex-snapshot
Targeted Inhibition of Hsp90 in Combination with Metformin Modulates Programmed Cell Death Pathways in A549 Lung Cancer Cells
inferred← citeshttps://doi.org/10.1007/s12010-026-05785-9openalex-snapshot
Feruloylated Arabinoxylan From Maize Bran Induces Cell Death in HCT 116 Colon Cancer Cells By the Cross-Talk of Apoptosis, Cell Survival, and Autophagy Pathways
inferred← citeshttps://doi.org/10.1007/s12031-013-0012-xopenalex-snapshot
Inhibition of Autophagy via p53-Mediated Disruption of ULK1 in a SCA7 Polyglutamine Disease Model
inferred← citeshttps://doi.org/10.1007/s12032-011-9916-xopenalex-snapshot
Cytoplasmic sequestration of wild-type p53 in a patient with therapy-related resistant AML: first report
inferred← citeshttps://doi.org/10.1007/s12032-024-02417-2openalex-snapshot
Dissecting the multifaceted roles of autophagy in cancer initiation, growth, and metastasis: from molecular mechanisms to therapeutic applications
inferred← citeshttps://doi.org/10.1007/s12035-013-8457-zopenalex-snapshot
Autophagy Modulation for Alzheimer’s Disease Therapy
inferred← citeshttps://doi.org/10.1007/s12035-014-8921-4openalex-snapshot
Mechanism and Regulation of Autophagy and Its Role in Neuronal Diseases
inferred← citeshttps://doi.org/10.1007/s12035-018-1277-4openalex-snapshot
Pathophysiological Roles of Intracellular Proteases in Neuronal Development and Neurological Diseases
inferred← citeshttps://doi.org/10.1007/s12035-025-05323-4openalex-snapshot
miR-133b-3p Mitigates D-Galactose-Induced Hippocampal Neuron Aging Through Autophagy Regulation via the MAPK/ERK Signaling Pathway
inferred← citeshttps://doi.org/10.1007/s12035-026-06062-wopenalex-snapshot
Targeting Sirtuin Signaling in Parkinson’s Disease and Neurodegeneration: Molecular Insights and Translational Potential
inferred← citeshttps://doi.org/10.1007/s12672-026-05143-5openalex-snapshot
Regulation of autophagy by the p53 family and the implications for cancer therapies
inferred← citeshttps://doi.org/10.1007/s13199-015-0374-7openalex-snapshot
Characterization of innate immunity genes in the parasitic nematode Brugia malayi
inferred← citeshttps://doi.org/10.1007/s13277-014-2660-zopenalex-snapshot
EGFR inhibitors and autophagy in cancer treatment
inferred← citeshttps://doi.org/10.1007/s13277-015-3496-xopenalex-snapshot
Autophagy and its function in radiosensitivity
inferred← citeshttps://doi.org/10.1007/s13402-019-00452-0openalex-snapshot
Interplay between HSF1 and p53 signaling pathways in cancer initiation and progression: non-oncogene and oncogene addiction
inferred← citeshttps://doi.org/10.1007/s42764-020-00016-9openalex-snapshot
Autophagy and DNA damage repair
inferred← citeshttps://doi.org/10.1016/b978-0-12-404599-6.00014-7openalex-snapshot
Oxidative Stress and Cell Death in Cardiovascular Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-405529-2.00024-xopenalex-snapshot
The Interplay between Autophagy and Apoptosis
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/b978-0-12-801043-3.00010-8openalex-snapshot
Apoptosis and Autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.98757-9openalex-snapshot
The TP53 Tumor Suppressor Gene: Structure and Function☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-802936-7.00010-6openalex-snapshot
Mutant p53 Located in the Cytoplasm Inhibits Autophagy
inferred← citeshttps://doi.org/10.1016/b978-0-12-802937-4.00009-0openalex-snapshot
Autophagy Regulation by HMGB1 in Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-802937-4.00013-2openalex-snapshot
Role of Autophagy in Cancer Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-805253-2.00012-2openalex-snapshot
Autophagy and Stroke
inferred← citeshttps://doi.org/10.1016/b978-0-12-812146-7.00020-2openalex-snapshot
Silibinin Protects Ultraviolet B–Irradiated Skin by Balancing Apoptosis and Autophagy in Epidermis and Dermis
inferred← citeshttps://doi.org/10.1016/b978-0-12-815889-0.00017-9openalex-snapshot
Graphene-Triggered Autophagy: The Savior or Slayer
inferred← citeshttps://doi.org/10.1016/b978-0-12-819609-0.00001-8openalex-snapshot
Dual effect of autophagy in the regulation of cell-mediated cytotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00005-xopenalex-snapshot
Regulation of autophagy—transcriptional, posttranscriptional, translational, and posttranslational mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-12-822481-6.00010-4openalex-snapshot
Programmed cell death mechanisms and nanoparticle toxicity
inferred← citeshttps://doi.org/10.1016/b978-0-323-99879-6.00006-7openalex-snapshot
Autophagy and metabolic regulation in cancer and its application in drug discovery
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0881-3.00010-3openalex-snapshot
Epidemiology and Molecular Mechanisms of Hepatocarcinogenesis
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4066-6.00014-7openalex-snapshot
Apoptosis, Necrosis, and Autophagy
inferred← citeshttps://doi.org/10.1016/bs.acr.2016.01.005openalex-snapshot
The Evolving, Multifaceted Roles of Autophagy in Cancer
inferred← citeshttps://doi.org/10.1016/bs.acr.2021.01.002openalex-snapshot
Autophagy and senescence in cancer therapy
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2016.04.004openalex-snapshot
Metabolic and Signaling Functions of Cancer Cell-Derived Extracellular Vesicles
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2026.07.001openalex-snapshot
Autophagy in oral cancer: New pathways-new roles
inferred← citeshttps://doi.org/10.1016/j.acthis.2017.03.007openalex-snapshot
Nanomicelle curcumin-induced DNA fragmentation in testicular tissue; Correlation between mitochondria dependent apoptosis and failed PCNA-related hemostasis
inferred← citeshttps://doi.org/10.1016/j.algal.2022.102820openalex-snapshot
Bioactive phlorotannin as autophagy modulator in cervical cancer cells and advanced glycation end products inhibitor in glucotoxic C. elegans
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741178openalex-snapshot
Unveiling the molecular regulatory mechanisms of immune responses in the spleen of spotted sea bass (Lateolabrax maculatus) against Nocardia seriolae infection
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2015.09.014openalex-snapshot
Radiotherapy-induced salivary dysfunction: Structural changes, pathogenetic mechanisms and therapies
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2021.105321openalex-snapshot
The two faces of autophagy in oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.arr.2011.09.001openalex-snapshot
Morphological and biochemical studies on aging and autophagy
inferred← citeshttps://doi.org/10.1016/j.arr.2012.05.001openalex-snapshot
Autophagy and ageing: Insights from invertebrate model organisms
inferred← citeshttps://doi.org/10.1016/j.arr.2014.07.001openalex-snapshot
The mitochondrial genome in aging and senescence
inferred← citeshttps://doi.org/10.1016/j.arr.2015.07.009openalex-snapshot
Selective multifaceted E3 ubiquitin ligases barricade extreme defense: Potential therapeutic targets for neurodegeneration and ageing
inferred← citeshttps://doi.org/10.1016/j.arr.2016.08.004openalex-snapshot
Anti-aging pharmacology: Promises and pitfalls
inferred← citeshttps://doi.org/10.1016/j.bbabio.2015.04.010openalex-snapshot
Mitochondria, autophagy and age-associated neurodegenerative diseases: New insights into a complex interplay
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.12.015openalex-snapshot
p53 and mitochondrial function in neurons
inferred← citeshttps://doi.org/10.1016/j.bbagen.2014.11.007openalex-snapshot
Psammaplin A induces Sirtuin 1-dependent autophagic cell death in doxorubicin-resistant MCF-7/adr human breast cancer cells and xenografts
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2025.195131openalex-snapshot
Autophagy-related genes and encoded proteins' prognostic significance in various cancer types: A molecular perspective
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.07.014openalex-snapshot
Autophagy: A lysosomal degradation pathway with a central role in health and disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.010openalex-snapshot
Autophagy in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.013openalex-snapshot
Role and regulation of autophagy in cancer
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2009.01.006openalex-snapshot
Anti- and pro-tumor functions of autophagy
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.11.016openalex-snapshot
Nuclear proteins acting on mitochondria
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.03.020openalex-snapshot
PRIMA-1 induces autophagy in cancer cells carrying mutant or wild type p53
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.05.022openalex-snapshot
The role of ubiquitin modification in the regulation of p53
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.2018.06.011openalex-snapshot
mTORC1 pathway in DNA damage response
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.02.009openalex-snapshot
Mechanical insights into the regulation of programmed cell death by p53 via mitochondria
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119482openalex-snapshot
Molecular mechanisms of microRNAs in glioblastoma pathogenesis
inferred← citeshttps://doi.org/10.1016/j.bbcan.2010.07.003openalex-snapshot
Autophagy is a therapeutic target in anticancer drug resistance
inferred← citeshttps://doi.org/10.1016/j.bbcan.2021.188565openalex-snapshot
Cross talk between autophagy and oncogenic signaling pathways and implications for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.03.095openalex-snapshot
Upregulation of Beclin-1 expression and phosphorylation of Bcl-2 and p53 are involved in the JNK-mediated autophagic cell death
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.08.121openalex-snapshot
Ursodeoxycholic acid modulates the ubiquitin-proteasome degradation pathway of p53
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.12.106openalex-snapshot
ARP101, a selective MMP-2 inhibitor, induces autophagy-associated cell death in cancer cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.10.054openalex-snapshot
Inhibition of autophagy stimulate molecular iodine-induced apoptosis in hormone independent breast tumors
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.05.059openalex-snapshot
Genetic analysis of SIRT1 gene promoter in sporadic Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.02.130openalex-snapshot
Electron microscopic visualization of autophagosomes induced by infection of human papillomavirus pseudovirions
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.07.037openalex-snapshot
AS-2, a novel inhibitor of p53-dependent apoptosis, prevents apoptotic mitochondrial dysfunction in a transcription-independent manner and protects mice from a lethal dose of ionizing radiation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.11.073openalex-snapshot
Disrupted cell cycle arrest and reduced proliferation in corneal fibroblasts from GCD2 patients: A potential role for altered autophagy flux
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