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TFEB and TFE3 are novel components of the integrated stress response

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What this work says

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

inferredcites →https://doi.org/10.1007/978-94-017-9211-0_18openalex-snapshot
The Role of Tumor Suppressor p53 in the Antioxidant Defense and Metabolism
inferredcites →https://doi.org/10.1007/s00018-014-1565-8openalex-snapshot
Novel roles for the MiTF/TFE family of transcription factors in organelle biogenesis, nutrient sensing, and energy homeostasis
inferredcites →https://doi.org/10.1007/s10495-014-0967-2openalex-snapshot
Autophagy and apoptosis: where do they meet?
inferredcites →https://doi.org/10.1016/j.bbrc.2008.12.079openalex-snapshot
ATF4 is necessary and sufficient for ER stress-induced upregulation of REDD1 expression
inferredcites →https://doi.org/10.1016/j.biocel.2007.01.020openalex-snapshot
Activating transcription factor 4
inferredcites →https://doi.org/10.1016/j.biochi.2010.02.020openalex-snapshot
Molecular mechanisms involved in the adaptation to amino acid limitation in mammals
inferredcites →https://doi.org/10.1016/j.cell.2010.02.024openalex-snapshot
Ragulator-Rag Complex Targets mTORC1 to the Lysosomal Surface and Is Necessary for Its Activation by Amino Acids
inferredcites →https://doi.org/10.1016/j.cell.2012.07.032openalex-snapshot
Ragulator Is a GEF for the Rag GTPases that Signal Amino Acid Levels to mTORC1
inferredcites →https://doi.org/10.1016/j.cell.2013.03.012openalex-snapshot
Exit from Pluripotency Is Gated by Intracellular Redistribution of the bHLH Transcription Factor Tfe3
inferredcites →https://doi.org/10.1016/j.cellsig.2014.08.015openalex-snapshot
Protein kinase RNA-like endoplasmic reticulum kinase (PERK)/calcineurin signaling is a novel pathway regulating intracellular calcium accumulation which might be involved in ventricular arrhythmias in diabetic cardiomyopathy
inferredcites →https://doi.org/10.1016/j.devcel.2011.07.016openalex-snapshot
Transcriptional Activation of Lysosomal Exocytosis Promotes Cellular Clearance
inferredcites →https://doi.org/10.1016/j.prp.2009.01.005openalex-snapshot
Altered expression of key cell cycle regulators in renal cell carcinoma associated with Xp11.2 translocation
inferredcites →https://doi.org/10.1016/j.yexcr.2006.09.015openalex-snapshot
Tfe3 expression is closely associated to macrophage terminal differentiation of human hematopoietic myeloid precursors
inferredcites →https://doi.org/10.1016/s1097-2765(00)00108-8openalex-snapshot
Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells
inferredcites →https://doi.org/10.1016/s1097-2765(03)00105-9openalex-snapshot
An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress
inferredcites →https://doi.org/10.1038/emboj.2012.32openalex-snapshot
A lysosome‐to‐nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB
inferredcites →https://doi.org/10.1038/nature14587openalex-snapshot
Transcriptional control of autophagy–lysosome function drives pancreatic cancer metabolism
inferredcites →https://doi.org/10.1038/nbt.2647openalex-snapshot
DNA targeting specificity of RNA-guided Cas9 nucleases
inferredcites →https://doi.org/10.1038/ncb0311-184openalex-snapshot
Integrating the mechanisms of apoptosis induced by endoplasmic reticulum stress
inferredcites →https://doi.org/10.1038/ncb2718openalex-snapshot
TFEB controls cellular lipid metabolism through a starvation-induced autoregulatory loop
inferredcites →https://doi.org/10.1038/ncb3114openalex-snapshot
Lysosomal calcium signalling regulates autophagy through calcineurin and TFEB
inferredcites →https://doi.org/10.1038/nrm3270openalex-snapshot
The unfolded protein response: controlling cell fate decisions under ER stress and beyond
inferredcites →https://doi.org/10.1042/bst0340007openalex-snapshot
Coping with stress: eIF2 kinases and translational control
inferredcites →https://doi.org/10.1053/j.semdp.2015.02.003openalex-snapshot
MiT family translocation renal cell carcinoma
inferredcites →https://doi.org/10.1073/pnas.0807611106openalex-snapshot
ERAD inhibitors integrate ER stress with an epigenetic mechanism to activate BH3-only protein NOXA in cancer cells
inferredcites →https://doi.org/10.1074/jbc.m113.503664openalex-snapshot
Insulin Secretion and Ca2+ Dynamics in β-Cells Are Regulated by PERK (EIF2AK3) in Concert with Calcineurin
inferredcites →https://doi.org/10.1074/jbc.m404559200openalex-snapshot
Preservation of Liver Protein Synthesis during Dietary Leucine Deprivation Occurs at the Expense of Skeletal Muscle Mass in Mice Deleted for eIF2 Kinase GCN2
inferredcites →https://doi.org/10.1083/jcb.201209135openalex-snapshot
Rag GTPases mediate amino acid–dependent recruitment of TFEB and MITF to lysosomes
inferredcites →https://doi.org/10.1111/j.1365-2818.2006.01706.xopenalex-snapshot
A guided tour into subcellular colocalization analysis in light microscopy
inferredcites →https://doi.org/10.1126/science.1157535openalex-snapshot
The Rag GTPases Bind Raptor and Mediate Amino Acid Signaling to mTORC1
inferredcites →https://doi.org/10.1126/science.1174447openalex-snapshot
A Gene Network Regulating Lysosomal Biogenesis and Function
inferredcites →https://doi.org/10.1126/science.1204592openalex-snapshot
TFEB Links Autophagy to Lysosomal Biogenesis
inferredcites →https://doi.org/10.1126/science.1247005openalex-snapshot
Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells
inferredcites →https://doi.org/10.1126/scisignal.2002790openalex-snapshot
The Transcription Factor TFEB Links mTORC1 Signaling to Transcriptional Control of Lysosome Homeostasis
inferredcites →https://doi.org/10.1126/scisignal.2004754openalex-snapshot
The Nutrient-Responsive Transcription Factor TFE3 Promotes Autophagy, Lysosomal Biogenesis, and Clearance of Cellular Debris
inferredcites →https://doi.org/10.1128/mcb.18.12.6930openalex-snapshot
Targeting the Microphthalmia Basic Helix-Loop-Helix–Leucine Zipper Transcription Factor to a Subset of E-Box Elements In Vitro and In Vivo
inferredcites →https://doi.org/10.1146/annurev.biochem.73.011303.074134openalex-snapshot
THE MAMMALIAN UNFOLDED PROTEIN RESPONSE
inferredcites →https://doi.org/10.1146/annurev.micro.59.031805.133833openalex-snapshot
TRANSLATIONAL REGULATION OFGCN4AND THE GENERAL AMINO ACID CONTROL OF YEAST
inferredcites →https://doi.org/10.1152/ajpcell.00594.2008openalex-snapshot
Effects of thapsigargin and phenylephrine on calcineurin and protein kinase C signaling functions in cardiac myocytes
inferredcites →https://doi.org/10.1155/2014/925350openalex-snapshot
FOXO Transcription Factors: Their Clinical Significance and Regulation
inferredcites →https://doi.org/10.1182/blood-2012-02-404475openalex-snapshot
NFAT control of innate immunity
inferredcites →https://doi.org/10.1371/journal.pone.0011925openalex-snapshot
Calcineurin Interacts with PERK and Dephosphorylates Calnexin to Relieve ER Stress in Mammals and Frogs
inferredcites →https://doi.org/10.1523/jneurosci.1598-10.2010openalex-snapshot
Neuronal Apoptosis Induced by Endoplasmic Reticulum Stress Is Regulated by ATF4–CHOP-Mediated Induction of the Bcl-2 Homology 3-Only Member PUMA
inferredcites →https://doi.org/10.3945/an.112.002113openalex-snapshot
Eukaryotic Initiation Factor 2 Phosphorylation and Translational Control in Metabolism
inferredcites →https://doi.org/10.4161/auto.19653openalex-snapshot
MTORC1 functions as a transcriptional regulator of autophagy by preventing nuclear transport of TFEB

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.4648361openalex-extracted
eIF2α Phosphorylation-Mediated Transcriptional Reprogramming Suppresses Impairment of Mitochondrial and GSH Homeostasis and Thereby Ferroptosis During ER Stress
inferred← citeshttps://doi.org/10.1002/9781119783435.ch22openalex-snapshot
CO as a Protective Mediator of Liver Injury
inferred← citeshttps://doi.org/10.1002/advs.202400666openalex-snapshot
CDK4/6 Inhibitors Impede Chemoresistance and Inhibit Tumor Growth of Small Cell Lung Cancer
inferred← citeshttps://doi.org/10.1002/bab.2104openalex-snapshot
The interplay of ROS and the PI3K/Akt pathway in autophagy regulation
inferred← citeshttps://doi.org/10.1002/ctm2.1272openalex-snapshot
ATP13A2 activates the pentose phosphate pathway to promote colorectal cancer growth though TFEB‐PGD axis
inferred← citeshttps://doi.org/10.1002/ctm2.797openalex-snapshot
Both SUMOylation and ubiquitination of TFE3 fusion protein regulated by androgen receptor are the potential target in the therapy of Xp11.2 translocation renal cell carcinoma
inferred← citeshttps://doi.org/10.1002/jat.4609openalex-snapshot
Mitophagy and its regulatory mechanisms in the biological effects of nanomaterials
inferred← citeshttps://doi.org/10.1002/jcb.30274openalex-snapshot
Targeting the lysosome: Mechanisms and treatments for nonalcoholic fatty liver disease
inferred← citeshttps://doi.org/10.1002/pmic.201800244openalex-snapshot
Proteomic Profiling of Iron‐Treated Ovarian Cells Identifies AKT Activation that Modulates the CLEAR Network
inferred← citeshttps://doi.org/10.1002/smll.202204310openalex-snapshot
Silica Nanoparticles Trigger Chaperone HSPB8‐Assisted Selective Autophagy via TFEB Activation in Hepatocytes
inferred← citeshttps://doi.org/10.1007/978-3-319-96704-2_6openalex-snapshot
The Lysosome and Intracellular Signalling
inferred← citeshttps://doi.org/10.1007/978-981-10-4801-2_77openalex-snapshot
Expression of Transcription Factor EB (TFEB) Promotes Cancer Cell Proliferation, Migration and Invasion
inferred← citeshttps://doi.org/10.1007/s00018-024-05286-0openalex-snapshot
Redox regulation of UPR signalling and mitochondrial ER contact sites
inferred← citeshttps://doi.org/10.1007/s00535-022-01889-1openalex-snapshot
Targeting autophagy as a therapeutic strategy against pancreatic cancer
inferred← citeshttps://doi.org/10.1007/s11010-021-04187-1openalex-snapshot
Elucidation of brefeldin A-induced ER and Golgi stress responses in Neuro2a cells
inferred← citeshttps://doi.org/10.1007/s11481-021-09990-7openalex-snapshot
Lysosomal Stress Response (LSR): Physiological Importance and Pathological Relevance
inferred← citeshttps://doi.org/10.1007/s12035-022-02895-3openalex-snapshot
The Regulation of MiTF/TFE Transcription Factors Across Model Organisms: from Brain Physiology to Implication for Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s12035-023-03503-8openalex-snapshot
FGF-18 Protects the Injured Spinal cord in mice by Suppressing Pyroptosis and Promoting Autophagy via the AKT-mTOR-TRPML1 axis
inferred← citeshttps://doi.org/10.1016/b978-0-12-815389-5.00040-xopenalex-snapshot
Homeostasis of solute and water by the transplanted kidney
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/bs.acr.2021.01.004openalex-snapshot
The role of autophagy in escaping therapy-induced polyploidy/senescence
inferred← citeshttps://doi.org/10.1016/bs.mcb.2020.10.017openalex-snapshot
Monitoring TFEB translocation
inferred← citeshttps://doi.org/10.1016/bs.mie.2016.10.008openalex-snapshot
Methods to Monitor and Manipulate TFEB Activity During Autophagy
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101203openalex-snapshot
The dialogue between the ubiquitin-proteasome system and autophagy: Implications in ageing
inferred← citeshttps://doi.org/10.1016/j.arr.2023.101985openalex-snapshot
TFEB is a central regulator of the aging process and age-related diseases
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.04.003openalex-snapshot
NCLs and ER: A stressful relationship
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.01.018openalex-snapshot
Arsenic trioxide induces autophagic cell death in osteosarcoma cells via the ROS-TFEB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.03.081openalex-snapshot
Inhibition of autophagy sensitizes lignan-induced endoplasmic reticulum stress-mediated cell death
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.03.118openalex-snapshot
Blue light-emitting diode irradiation promotes transcription factor EB-mediated lysosome biogenesis and lysosomal cell death in murine photoreceptor-derived cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.154077openalex-snapshot
High-content screening identifies mTORC1-independent TFEB activators that promote protective autophagy
inferred← citeshttps://doi.org/10.1016/j.bcp.2018.11.016openalex-snapshot
Clomiphene citrate induces nuclear translocation of the TFEB transcription factor and triggers apoptosis by enhancing lysosomal membrane permeabilization
inferred← citeshttps://doi.org/10.1016/j.bcp.2024.116277openalex-snapshot
Risk factors of using late-autophagy inhibitors: Aspects to consider when combined with anticancer therapies
inferred← citeshttps://doi.org/10.1016/j.bcp.2026.117915openalex-snapshot
Targeting PERK signaling: mechanisms and roles in myocardial protection
inferred← citeshttps://doi.org/10.1016/j.biopha.2020.110272openalex-snapshot
Emerging role of transcription factor EB in mitochondrial quality control
inferred← citeshttps://doi.org/10.1016/j.brainres.2016.04.042openalex-snapshot
ER stress and Parkinson's disease: Pathological inputs that converge into the secretory pathway
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216599openalex-snapshot
Emerging roles of lysosome homeostasis (repair, lysophagy and biogenesis) in cancer progression and therapy
inferred← citeshttps://doi.org/10.1016/j.cbi.2022.109963openalex-snapshot
Upregulation of the TFEB-mediated lysosome function relieves 4-Hydroxynonenal-Induced apoptosis
inferred← citeshttps://doi.org/10.1016/j.cell.2018.10.044openalex-snapshot
Spatiotemporal Control of CNS Myelination by Oligodendrocyte Programmed Cell Death through the TFEB-PUMA Axis
inferred← citeshttps://doi.org/10.1016/j.cellsig.2021.110134openalex-snapshot
Calcineurin in the heart: New horizons for an old friend
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110796openalex-snapshot
Lipogenesis mediated by OGR1 regulates metabolic adaptation to acid stress in cancer cells via autophagy
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114872openalex-snapshot
USP7 protects TFEB from proteasome-mediated degradation
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116499openalex-snapshot
MITF, TFEB, and TFE3 drive distinct adaptive gene expression programs and immune infiltration in melanoma
inferred← citeshttps://doi.org/10.1016/j.cophys.2022.100591openalex-snapshot
Transcriptional regulation of autophagy in aging
inferred← citeshttps://doi.org/10.1016/j.currproblcancer.2021.100773openalex-snapshot
Kidney cancer: from genes to therapy
inferred← citeshttps://doi.org/10.1016/j.dci.2025.105480openalex-snapshot
Lamprey TFE3 exhibits evolutionarily conserved activation mechanisms and regulates autophagy and immune responses
inferred← citeshttps://doi.org/10.1016/j.devcel.2017.12.020openalex-snapshot
A Futile Battle? Protein Quality Control and the Stress of Aging
inferred← citeshttps://doi.org/10.1016/j.devcel.2018.10.003openalex-snapshot
The Lysosomal Transcription Factor TFEB Represses Myelination Downstream of the Rag-Ragulator Complex
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.06.010openalex-snapshot
The Lysosome at the Intersection of Cellular Growth and Destruction
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.07.004openalex-snapshot
Sestrin2 drives ER-phagy in response to protein misfolding
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.114674openalex-snapshot
TFE3-mediated impairment of lysosomal biogenesis and defective autophagy contribute to fluoride-induced hepatotoxicity
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.05.401openalex-snapshot
TFEB orchestrates ferritinophagy and ferroptosis in ionophore drug-induced hepatotoxicity: unveiling a novel therapeutic avenue
inferred← citeshttps://doi.org/10.1016/j.immuni.2026.07.008openalex-snapshot
Lysosomal dysfunction drives a transcriptional and epigenetic signature found in disease-associated microglia in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.isci.2020.101691openalex-snapshot
c-Abl Inhibition Activates TFEB and Promotes Cellular Clearance in a Lysosomal Disorder
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106169openalex-snapshot
Beta-coronaviruses exploit cellular stress responses by modulating TFEB and TFE3 activity
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101740openalex-snapshot
Inositol triphosphate–triggered calcium release from the endoplasmic reticulum induces lysosome biogenesis via TFEB/TFE3
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2023.109325openalex-snapshot
Activation of ROS-PERK-TFEB by filbertone ameliorates neurodegenerative diseases via enhancing the autophagy-lysosomal pathway
inferred← citeshttps://doi.org/10.1016/j.lfs.2020.117341openalex-snapshot
The role of TFEB in tumor cell autophagy: Diagnostic and therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.lfs.2022.120888openalex-snapshot
LIMP2 gene, evolutionarily conserved regulation by TFE3, relieves lysosomal stress induced by cholesterol
inferred← citeshttps://doi.org/10.1016/j.metabol.2023.155662openalex-snapshot
Transcription factor EB: A potential integrated network regulator in metabolic-associated cardiac injury
inferred← citeshttps://doi.org/10.1016/j.mocell.2024.100176openalex-snapshot
eIF2α phosphorylation-ATF4 axis-mediated transcriptional reprogramming mitigates mitochondrial impairment during ER stress
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.12.027openalex-snapshot
Epigenetic Control of Autophagy: Nuclear Events Gain More Attention
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.03.023openalex-snapshot
Autophagy in cancer cell remodeling and quality control
inferred← citeshttps://doi.org/10.1016/j.molcel.2022.08.005openalex-snapshot
Life in lockdown: Orchestrating endoplasmic reticulum and lysosome homeostasis for quiescent cells
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.01.012openalex-snapshot
The GATOR2 complex maintains lysosomal-autophagic function by inhibiting the protein degradation of MiT/TFEs
inferred← citeshttps://doi.org/10.1016/j.molcel.2026.01.011openalex-snapshot
Lysosomes as hubs of metabolic sensing and cellular homeostasis
inferred← citeshttps://doi.org/10.1016/j.nbd.2022.105615openalex-snapshot
APOE4 confers transcriptomic and functional alterations to primary mouse microglia
inferred← citeshttps://doi.org/10.1016/j.phymed.2023.154720openalex-snapshot
Trigonochinene E promotes lysosomal biogenesis and enhances autophagy via TFEB/TFE3 in human degenerative NP cells against oxidative stress
inferred← citeshttps://doi.org/10.1016/j.pmatsci.2025.101644openalex-snapshot
Nanoplatform-Guided modulation of organelle dynamics: mechanistic insights and therapeutic strategies
inferred← citeshttps://doi.org/10.1016/j.redox.2020.101445openalex-snapshot
A stress response p38 MAP kinase inhibitor SB202190 promoted TFEB/TFE3-dependent autophagy and lysosomal biogenesis independent of p38
inferred← citeshttps://doi.org/10.1016/j.smim.2025.101954openalex-snapshot
Endoplasmic reticulum stress: A key player in immune cell regulation and autoimmune disorders
inferred← citeshttps://doi.org/10.1016/j.tcb.2021.12.009openalex-snapshot
Built to last: lysosome remodeling and repair in health and disease
inferred← citeshttps://doi.org/10.1016/j.tibs.2020.09.004openalex-snapshot
How Lysosomes Sense, Integrate, and Cope with Stress
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.05.014openalex-snapshot
Ligand-activated progesterone receptor B activates transcription factor EB to promote autophagy in human breast cancer cells
inferred← citeshttps://doi.org/10.1038/s12276-025-01579-xopenalex-snapshot
Failure of lysosomal acidification and endomembrane network in neurodegeneration
inferred← citeshttps://doi.org/10.1038/s41388-019-0930-3openalex-snapshot
RETRACTED ARTICLE: Synergy between arsenic trioxide and JQ1 on autophagy in pancreatic cancer
inferred← citeshttps://doi.org/10.1038/s41388-022-02206-zopenalex-snapshot
HSP90 inhibitors induce GPNMB cell-surface expression by modulating lysosomal positioning and sensitize breast cancer cells to glembatumumab vedotin
inferred← citeshttps://doi.org/10.1038/s41401-021-00711-7openalex-snapshot
TFEB, a master regulator of autophagy and biogenesis, unexpectedly promotes apoptosis in response to the cyclopentenone prostaglandin 15d-PGJ2
inferred← citeshttps://doi.org/10.1038/s41401-026-01762-4openalex-snapshot
MCOLN1-mediated PPP3CB activation alleviates neuronal damage by promoting TFEB-dependent autophagic flux in permanent cerebral ischemia
inferred← citeshttps://doi.org/10.1038/s41413-025-00427-yopenalex-snapshot
ER-induced PERK/TFEB cascade sequentially modulates mitochondrial dynamics during cranial suture expansion
inferred← citeshttps://doi.org/10.1038/s41418-022-01028-6openalex-snapshot
Past, present, and future perspectives of transcription factor EB (TFEB): mechanisms of regulation and association with disease
inferred← citeshttps://doi.org/10.1038/s41418-024-01378-3openalex-snapshot
Integrated stress response plasticity governs normal cell adaptation to chronic stress via the PP2A-TFE3-ATF4 pathway
inferred← citeshttps://doi.org/10.1038/s41419-018-0917-yopenalex-snapshot
SARS-Coronavirus Open Reading Frame-3a drives multimodal necrotic cell death
inferred← citeshttps://doi.org/10.1038/s41419-018-1112-xopenalex-snapshot
Carbon monoxide-induced TFEB nuclear translocation enhances mitophagy/mitochondrial biogenesis in hepatocytes and ameliorates inflammatory liver injury
inferred← citeshttps://doi.org/10.1038/s41419-019-1478-4openalex-snapshot
Keratinocyte differentiation promotes ER stress-dependent lysosome biogenesis
inferred← citeshttps://doi.org/10.1038/s41419-020-03357-1openalex-snapshot
Arsenic trioxide induces macrophage autophagy and atheroprotection by regulating ROS-dependent TFEB nuclear translocation and AKT/mTOR pathway
inferred← citeshttps://doi.org/10.1038/s41419-024-06547-3openalex-snapshot
mTOR pathway occupies a central role in the emergence of latent cancer cells
inferred← citeshttps://doi.org/10.1038/s41420-019-0181-7openalex-snapshot
SARS-Coronavirus Open Reading Frame-8b triggers intracellular stress pathways and activates NLRP3 inflammasomes
inferred← citeshttps://doi.org/10.1038/s41420-025-02530-9openalex-snapshot
CO confers neuroprotection via activating the PERK-calcineurin pathway and inhibiting necroptosis
inferred← citeshttps://doi.org/10.1038/s41467-017-01871-zopenalex-snapshot
TFEB regulates lysosomal positioning by modulating TMEM55B expression and JIP4 recruitment to lysosomes
inferred← citeshttps://doi.org/10.1038/s41467-017-02332-3openalex-snapshot
Small-molecule TFEB pathway agonists that ameliorate metabolic syndrome in mice and extend C. elegans lifespan
inferred← citeshttps://doi.org/10.1038/s41467-018-04849-7openalex-snapshot
A TFEB nuclear export signal integrates amino acid supply and glucose availability
inferred← citeshttps://doi.org/10.1038/s41467-019-11568-0openalex-snapshot
MYC competes with MiT/TFE in regulating lysosomal biogenesis and autophagy through an epigenetic rheostat
inferred← citeshttps://doi.org/10.1038/s41467-019-14038-9openalex-snapshot
Golgi organization is regulated by proteasomal degradation
inferred← citeshttps://doi.org/10.1038/s41467-023-37812-2openalex-snapshot
A bacterial autotransporter impairs innate immune responses by targeting the transcription factor TFE3
inferred← citeshttps://doi.org/10.1038/s41467-025-63022-zopenalex-snapshot
Dysregulation of GTPase-activating protein-binding protein1 in the pathogenesis of metabolic dysfunction-associated steatotic liver disease
inferred← citeshttps://doi.org/10.1038/s41467-026-71001-1openalex-snapshot
TFEB degradation is regulated by an IKK/β-TrCP2 phosphorylation-ubiquitination cascade
inferred← citeshttps://doi.org/10.1038/s41531-024-00760-9openalex-snapshot
PDCD4 triggers α-synuclein accumulation and motor deficits via co-suppressing TFE3 and TFEB translation in a model of Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41556-018-0244-7openalex-snapshot
The lysosome as a cellular centre for signalling, metabolism and quality control
inferred← citeshttps://doi.org/10.1038/s41556-020-0535-7openalex-snapshot
Endocytic regulation of cellular ion homeostasis controls lysosome biogenesis
inferred← citeshttps://doi.org/10.1038/s41556-023-01197-7openalex-snapshot
Balancing lysosome abundance in health and disease
inferred← citeshttps://doi.org/10.1038/s41580-019-0185-4openalex-snapshot
Lysosomes as dynamic regulators of cell and organismal homeostasis
inferred← citeshttps://doi.org/10.1038/s41580-023-00676-xopenalex-snapshot
Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology
inferred← citeshttps://doi.org/10.1038/s41581-026-01082-0openalex-snapshot
Selective autophagy in kidney health and disease
inferred← citeshttps://doi.org/10.1038/s41588-023-01397-9openalex-snapshot
Integrating genetics with single-cell multiomic measurements across disease states identifies mechanisms of beta cell dysfunction in type 2 diabetes
inferred← citeshttps://doi.org/10.1038/s41593-023-01494-2openalex-snapshot
TFEB–vacuolar ATPase signaling regulates lysosomal function and microglial activation in tauopathy
inferred← citeshttps://doi.org/10.1038/s41598-024-64579-3openalex-snapshot
Blockage of Akt activation suppresses cadmium-induced renal tubular cellular damages through aggrephagy in HK-2 cells
inferred← citeshttps://doi.org/10.1038/s42003-021-02278-9openalex-snapshot
Genotoxic stress in constitutive trisomies induces autophagy and the innate immune response via the cGAS-STING pathway
inferred← citeshttps://doi.org/10.1038/s42003-025-07870-xopenalex-snapshot
Investigation of dynamic regulation of TFEB nuclear shuttling by microfluidics and quantitative modelling
inferred← citeshttps://doi.org/10.1038/s42255-021-00368-wopenalex-snapshot
TFEB–GDF15 axis protects against obesity and insulin resistance as a lysosomal stress response
inferred← citeshttps://doi.org/10.1038/s43587-023-00524-9openalex-snapshot
A drug-like molecule engages nuclear hormone receptor DAF-12/FXR to regulate mitophagy and extend lifespan
inferred← citeshttps://doi.org/10.1038/s44318-024-00233-yopenalex-snapshot
Non-autophagic Golgi-LC3 lipidation facilitates TFE3 stress response against Golgi dysfunction
inferred← citeshttps://doi.org/10.1038/s44318-024-00338-4openalex-snapshot
The integrated stress response drives MET oncogene overexpression in cancers
inferred← citeshttps://doi.org/10.1038/s44319-024-00339-8openalex-snapshot
The proximity-based protein interactome and regulatory logics of the transcription factor p65 NF-κB/RELA
inferred← citeshttps://doi.org/10.1038/s44319-025-00659-3openalex-snapshot
Differential contribution of TFE3 isoforms to cell motility and invasion
inferred← citeshttps://doi.org/10.1042/bcj20190596openalex-snapshot
A lysosome independent role for TFEB in activating DNA repair and inhibiting apoptosis in breast cancer cells
inferred← citeshttps://doi.org/10.1073/pnas.2122170119openalex-snapshot
False-positive IRESes from Hoxa9 and other genes resulting from errors in mammalian 5′ UTR annotations
inferred← citeshttps://doi.org/10.1074/jbc.ra118.003471openalex-snapshot
Protein phosphatase 2A stimulates activation of TFEB and TFE3 transcription factors in response to oxidative stress
inferred← citeshttps://doi.org/10.1074/jbc.ra119.011864openalex-snapshot
The gene for the lysosomal protein LAMP3 is a direct target of the transcription factor ATF4
inferred← citeshttps://doi.org/10.1080/10715762.2018.1485075openalex-snapshot
Inhibiting ROS-TFE3-dependent autophagy enhances the therapeutic response to metformin in breast cancer
inferred← citeshttps://doi.org/10.1080/15548627.2018.1463120openalex-snapshot
TRIM37 deficiency induces autophagy through deregulating the MTORC1-TFEB axis
inferred← citeshttps://doi.org/10.1080/15548627.2018.1531198openalex-snapshot
AKT inhibition-mediated dephosphorylation of TFE3 promotes overactive autophagy independent of MTORC1 in cadmium-exposed bone mesenchymal stem cells
inferred← citeshttps://doi.org/10.1080/15548627.2019.1704104openalex-snapshot
Oxidation of multiple MiT/TFE transcription factors links oxidative stress to transcriptional control of autophagy and lysosome biogenesis
inferred← citeshttps://doi.org/10.1080/15548627.2020.1788889openalex-snapshot
The unfolded protein response regulates hepatic autophagy by sXBP1-mediated activation of TFEB
inferred← citeshttps://doi.org/10.1080/15548627.2022.2029671openalex-snapshot
The FACT complex facilitates expression of lysosomal and antioxidant genes through binding to TFEB and TFE3
inferred← citeshttps://doi.org/10.1080/15548627.2022.2105561openalex-snapshot
Regulation of TFEB nuclear localization by HSP90AA1 promotes autophagy and longevity
inferred← citeshttps://doi.org/10.1080/15548627.2023.2173900openalex-snapshot
Phosphorylation of EIF2S1 (eukaryotic translation initiation factor 2 subunit alpha) is indispensable for nuclear translocation of TFEB and TFE3 during ER stress
inferred← citeshttps://doi.org/10.1080/15548627.2024.2305063openalex-snapshot
ANXA2 (annexin A2) is crucial to ATG7-mediated autophagy, leading to tumor aggressiveness in triple-negative breast cancer cells
inferred← citeshttps://doi.org/10.1080/15548627.2024.2334111openalex-snapshot
Design and validation of a reporter mouse to study the dynamic regulation of TFEB and TFE3 activity through in vivo imaging techniques
inferred← citeshttps://doi.org/10.1080/15548627.2025.2487036openalex-snapshot
TFEB and TFE3 regulate STING1-dependent immune responses by controlling type I interferon signaling
inferred← citeshttps://doi.org/10.1080/15548627.2026.2629720openalex-snapshot
AMPK promotes TFEB transcriptional activity through dephosphorylation at both MTORC1-dependent and -independent sites
inferred← citeshttps://doi.org/10.1080/21505594.2021.2021630openalex-snapshot
The endoplasmic reticulum stress-mediated unfolded protein response protects against infection of goat endometrial epithelial cells by Trueperella pyogenes via autophagy
inferred← citeshttps://doi.org/10.1080/21541248.2016.1218990openalex-snapshot
Rags to riches: Amino acid sensing by the Rag GTPases in health and disease
inferred← citeshttps://doi.org/10.1080/21541264.2016.1264353openalex-snapshot
TFEB and TFE3: The art of multi-tasking under stress conditions
inferred← citeshttps://doi.org/10.1080/27694127.2022.2097822openalex-snapshot
TFEBexplorer: An integrated tool to study genes regulated by the stress-responsive Transcription Factor EB
inferred← citeshttps://doi.org/10.1080/27694127.2025.2473765openalex-snapshot
High throughput screening assay for the identification of ATF4 and TFEB activating compounds
inferred← citeshttps://doi.org/10.1083/jcb.201611073openalex-snapshot
PtdIns3P controls mTORC1 signaling through lysosomal positioning
inferred← citeshttps://doi.org/10.1083/jcb.202102001openalex-snapshot
Lysosome biogenesis: Regulation and functions
inferred← citeshttps://doi.org/10.1083/jcb.202307079openalex-snapshot
ATG conjugation–dependent/independent mechanisms underlie lysosomal stress–induced TFEB regulation
inferred← citeshttps://doi.org/10.1083/jcb.202308099openalex-snapshot
Lactylation stabilizes TFEB to elevate autophagy and lysosomal activity
inferred← citeshttps://doi.org/10.1091/mbc.e21-06-0309openalex-snapshot
PP2A-dependent TFEB activation is blocked by PIKfyve-induced mTORC1 activity
inferred← citeshttps://doi.org/10.1097/pai.0000000000001090openalex-snapshot
Application of TFE3 Immunophenotypic and TFE3 mRNA Expressions in Diagnosis and Prognostication of Adrenal Cortical Neoplasms and Distinction From Kidney Tumors
inferred← citeshttps://doi.org/10.1101/2020.10.27.357897openalex-snapshot
Repression of lysosomal transcription factors Tfeb and Tfe3 is essential for the migration and function of microglia
inferred← citeshttps://doi.org/10.1101/2021.07.26.453823openalex-snapshot
ESCRT-I controls lysosomal membrane protein homeostasis and restricts MCOLN1-dependent TFEB/TFE3 signaling
inferred← citeshttps://doi.org/10.1101/2022.06.23.497394openalex-snapshot
Restoration of β-GC trafficking improves the lysosome function in Gaucher’s disease
inferred← citeshttps://doi.org/10.1101/2022.12.31.522386openalex-snapshot
Integration of single-cell multiomic measurements across disease states with genetics identifies mechanisms of beta cell dysfunction in type 2 diabetes
inferred← citeshttps://doi.org/10.1101/2024.01.22.576606openalex-snapshot
Lipid Dysregulation Unveil the Intricate Interplay of Lysosomal and Mitochondrial Changes in Frontotemporal Dementia with GRN Haploinsufficiency
inferred← citeshttps://doi.org/10.1101/2024.01.29.577876openalex-snapshot
Cellular Modeling of CLN6 with IPSC-derived Neurons and Glia
inferred← citeshttps://doi.org/10.1101/2024.06.05.597553openalex-snapshot
HLH-30/TFEB rewires the chaperone network to promote proteostasis under conditions of Coenzyme A and Iron-Sulfur Cluster Deficiency
inferred← citeshttps://doi.org/10.1101/2024.09.26.615214openalex-snapshot
Phospholipase D3 regulates lysosomal morphology, biogenesis, and function in neurons
inferred← citeshttps://doi.org/10.1101/2024.10.22.619589openalex-snapshot
AMPK activation promotes transcriptional activation of TFEB through its dephosphorylation
inferred← citeshttps://doi.org/10.1101/2024.11.12.623296openalex-snapshot
Mechanisms driving epigenetic and transcriptional responses of microglia in a neurodegenerative lysosomal storage disorder model
inferred← citeshttps://doi.org/10.1101/2025.01.28.635321openalex-snapshot
Endurance Training Restores Ageing-Impaired Lysosomal Biogenesis Factors in Rest and Response to Acute Exercise in Rat Skeletal Muscle
inferred← citeshttps://doi.org/10.1101/2025.09.05.674552openalex-snapshot
Peripheral inflammation mediates midbrain Lrrk2 kinase activity via Rab32 expression
inferred← citeshttps://doi.org/10.1101/312033openalex-snapshot
A non-canonical lysosome biogenesis pathway generates Golgi-associated lysosomes during epidermal differentiation
inferred← citeshttps://doi.org/10.1101/683359openalex-snapshot
Genome-wide functional genomics screens identify therapeutic vulnerabilities for lymphangioleiomyomatosis
inferred← citeshttps://doi.org/10.1101/gad.287953.116openalex-snapshot
The tumor suppressor FLCN mediates an alternate mTOR pathway to regulate browning of adipose tissue
inferred← citeshttps://doi.org/10.1101/gad.324657.119openalex-snapshot
MITF—the first 25 years
inferred← citeshttps://doi.org/10.1111/acel.12561openalex-snapshot
The amino acid transporter SLC36A4 regulates the amino acid pool in retinal pigmented epithelial cells and mediates the mechanistic target of rapamycin, complex 1 signaling
inferred← citeshttps://doi.org/10.1111/acel.12689openalex-snapshot
TOR ‐mediated regulation of metabolism in aging
inferred← citeshttps://doi.org/10.1111/acel.70038openalex-snapshot
HLH ‐30/ TFEB Rewires the Chaperone Network to Promote Proteostasis Upon Perturbations to the Coenzyme A and Iron–Sulfur Cluster Biosynthesis Pathways
inferred← citeshttps://doi.org/10.1111/bph.15702openalex-snapshot
Cyclic helix B peptide promotes random‐pattern skin flap survival via TFE3‐mediated enhancement of autophagy and reduction of ROS levels
inferred← citeshttps://doi.org/10.1111/brv.12860openalex-snapshot
The PERKs of mitochondria protection during stress: insights for PERK modulation in neurodegenerative and metabolic diseases
inferred← citeshttps://doi.org/10.1111/fcp.12634openalex-snapshot
Evaluating and modulating TFEB in the control of autophagy: toward new treatments in CNS disorders
inferred← citeshttps://doi.org/10.1111/imcb.70157openalex-snapshot
Lysosomal Rewiring Perpetuates Tumor Immune Evasion in Cancer
inferred← citeshttps://doi.org/10.1111/jcmm.14469openalex-snapshot
EIF2A promotes cell survival during paclitaxel treatment in vitro and in vivo
inferred← citeshttps://doi.org/10.1111/jcmm.18257openalex-snapshot
Huayu Qutan Recipe promotes lipophagy and cholesterol efflux through the mTORC1 / TFEB / ABCA1‐SCARB1 signal axis
inferred← citeshttps://doi.org/10.1111/jnc.14564openalex-snapshot
Lysosome biogenesis in health and disease
inferred← citeshttps://doi.org/10.1111/jre.70016openalex-snapshot
The Role of Oxidative Stress in Periodontitis
inferred← citeshttps://doi.org/10.1111/nyas.13131openalex-snapshot
Transcription factor EB: from master coordinator of lysosomal pathways to candidate therapeutic target in degenerative storage diseases
inferred← citeshttps://doi.org/10.1111/pcmr.13149openalex-snapshot
TFE3 promotes ferroptosis in melanoma
inferred← citeshttps://doi.org/10.1111/tra.12497openalex-snapshot
The big and intricate dreams of little organelles: Embracing complexity in the study of membrane traffic
inferred← citeshttps://doi.org/10.1111/tra.12552openalex-snapshot
Phagocytosis of antibody‐opsonized tumor cells leads to the formation of a discrete vacuolar compartment in macrophages
inferred← citeshttps://doi.org/10.1111/tra.12886openalex-snapshot
Pseudophosphatase STYXL1 depletion enhances glucocerebrosidase trafficking to lysosomes via ER stress
inferred← citeshttps://doi.org/10.1111/tra.12911openalex-snapshot
Restoration of β‐GC trafficking improves the lysosome function in Gaucher disease
inferred← citeshttps://doi.org/10.1111/tra.70013openalex-snapshot
FGF Signaling Promotes Lysosome Biogenesis in Chondrocytes via the Mannose Phosphate Receptor Pathway
inferred← citeshttps://doi.org/10.1113/ep093041openalex-snapshot
Mitophagy in skeletal muscle: Impact of ageing, exercise and disuse
inferred← citeshttps://doi.org/10.1126/sciadv.aaz9805openalex-snapshot
Lysosomal recycling of amino acids affects ER quality control
inferred← citeshttps://doi.org/10.1126/sciadv.abb0205openalex-snapshot
GADD34 is a modulator of autophagy during starvation
inferred← citeshttps://doi.org/10.1126/sciadv.abb9614openalex-snapshot
Beyond the cell factory: Homeostatic regulation of and by the UPR ER
inferred← citeshttps://doi.org/10.1126/sciadv.abp8321openalex-snapshot
A lysosomal regulatory circuit essential for the development and function of microglia
inferred← citeshttps://doi.org/10.1126/scisignal.aau2281openalex-snapshot
TFEB drives PGC-1α expression in adipocytes to protect against diet-induced metabolic dysfunction
inferred← citeshttps://doi.org/10.1128/mcb.00241-22openalex-snapshot
Invading Bacterial Pathogens Activate Transcription Factor EB in Epithelial Cells through the Amino Acid Starvation Pathway of mTORC1 Inhibition
inferred← citeshttps://doi.org/10.1128/mcb.00489-18openalex-snapshot
Isoginkgetin, a Natural Biflavonoid Proteasome Inhibitor, Sensitizes Cancer Cells to Apoptosis via Disruption of Lysosomal Homeostasis and Impaired Protein Clearance
inferred← citeshttps://doi.org/10.1136/jclinpath-2020-206899openalex-snapshot
Gene of the month: TFE 3
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-111315-125407openalex-snapshot
TFEB and TFE3: Linking Lysosomes to Cellular Adaptation to Stress
inferred← citeshttps://doi.org/10.1146/annurev-pharmtox-010716-104936openalex-snapshot
Autophagy: A Druggable Process
inferred← citeshttps://doi.org/10.1152/ajpcell.00080.2023openalex-snapshot
Activating transcription factor 4 regulates mitochondrial content, morphology, and function in differentiating skeletal muscle myotubes
inferred← citeshttps://doi.org/10.1152/ajpendo.00339.2020openalex-snapshot
Transcription factor EB and TFE3: new metabolic coordinators mediating adaptive responses to exercise in skeletal muscle?
inferred← citeshttps://doi.org/10.1152/ajpheart.00145.2017openalex-snapshot
Autophagy modulation: a potential therapeutic approach in cardiac hypertrophy
inferred← citeshttps://doi.org/10.1152/ajprenal.00237.2022openalex-snapshot
Functional TFEB activation characterizes multiple models of renal cystic disease and loss of polycystin-1
inferred← citeshttps://doi.org/10.1152/physiol.00048.2025openalex-snapshot
Organelle Dysfunction and TNT-Mediated Aggregate Spreading in Neurodegeneration
inferred← citeshttps://doi.org/10.1155/2020/8872639openalex-snapshot
Nutrient Sensor mTOR and OGT: Orchestrators of Organelle Homeostasis in Pancreatic β-Cells
inferred← citeshttps://doi.org/10.1155/2021/5583215openalex-snapshot
Reactive Oxygen Species as a Link between Antioxidant Pathways and Autophagy
inferred← citeshttps://doi.org/10.1155/2021/8186877openalex-snapshot
GDF‐11 Protects the Traumatically Injured Spinal Cord by Suppressing Pyroptosis and Necroptosis via TFE3‐Mediated Autophagy Augmentation
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-18-0269openalex-snapshot
Therapeutic Targeting of TFE3/IRS-1/PI3K/mTOR Axis in Translocation Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.1161/circresaha.121.319377openalex-snapshot
Alternative Mitophagy Protects the Heart Against Obesity-Associated Cardiomyopathy
inferred← citeshttps://doi.org/10.1172/jci.insight.132364openalex-snapshot
The UPR preserves mature oligodendrocyte viability and function in adults by regulating autophagy of PLP
inferred← citeshttps://doi.org/10.1172/jci.insight.194102openalex-snapshot
Restoration of impaired lysosomal function mitigates drusen-like deposit formation and cell death in Malattia Leventinese
inferred← citeshttps://doi.org/10.1172/jci176093openalex-snapshot
Small-molecule modulators of B56-PP2A restore 4E-BP function to suppress eIF4E-dependent translation in cancer cells
inferred← citeshttps://doi.org/10.1177/20503121231157209openalex-snapshot
Transcription factor EB as a key molecular factor in human health and its implication in diseases
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