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Mild uncoupling of mitochondria synergistically enhances senolytic specificity and sensitivity of BH3 mimetics

https://doi.org/10.1101/2023.08.23.554476
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1873-3468.13498openalex-snapshot
Mitochondrial dysfunction and cell senescence: deciphering a complex relationship
inferredcites →https://doi.org/10.1002/1878-0261.13312openalex-snapshot
Targeting senescence as an anticancer therapy
inferredcites →https://doi.org/10.1002/biof.5520080314openalex-snapshot
Imaging the mitochondrial permeability transition pore in intact cells
inferredcites →https://doi.org/10.1002/jcsm.12982openalex-snapshot
Mitochondrial uncoupling attenuates sarcopenic obesity by enhancing skeletal muscle mitophagy and quality control
inferredcites →https://doi.org/10.1007/s10541-005-0104-5openalex-snapshot
Lipophilic triphenylphosphonium cations as tools in mitochondrial bioenergetics and free radical biology
inferredcites →https://doi.org/10.1016/j.cmet.2019.05.006openalex-snapshot
Acceleration of β Cell Aging Determines Diabetes and Senolysis Improves Disease Outcomes
inferredcites →https://doi.org/10.1016/j.ebiom.2017.03.020openalex-snapshot
Mitochondria in Cell Senescence: Is Mitophagy the Weakest Link?
inferredcites →https://doi.org/10.1016/j.ebiom.2018.09.015openalex-snapshot
Fisetin is a senotherapeutic that extends health and lifespan
inferredcites →https://doi.org/10.1016/j.ebiom.2019.01.056openalex-snapshot
Senolytics and senostatics as adjuvant tumour therapy
inferredcites →https://doi.org/10.1016/j.ejphar.2019.172655openalex-snapshot
Current overview on the clinical update of Bcl-2 anti-apoptotic inhibitors for cancer therapy
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.06.005openalex-snapshot
Partial uncoupling of oxidative phosphorylation induces premature senescence in human fibroblasts and yeast mother cells
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2008.09.031openalex-snapshot
Mitochondrial complex I dysfunction in rat heart with aging: critical role of reactive oxygen species and cardiolipin
inferredcites →https://doi.org/10.1016/j.ijrobp.2017.02.216openalex-snapshot
Inhibition of Bcl-2/xl With ABT-263 Selectively Kills Senescent Type II Pneumocytes and Reverses Persistent Pulmonary Fibrosis Induced by Ionizing Radiation in Mice
inferredcites →https://doi.org/10.1016/j.mad.2005.11.004openalex-snapshot
Alterations in mitochondrial function, hydrogen peroxide release and oxidative damage in mouse hind-limb skeletal muscle during aging
inferredcites →https://doi.org/10.1016/j.mad.2019.03.006openalex-snapshot
Sublethal whole-body irradiation causes progressive premature frailty in mice
inferredcites →https://doi.org/10.1016/j.molcel.2014.10.028openalex-snapshot
Mitochondrial Shape Governs BAX-Induced Membrane Permeabilization and Apoptosis
inferredcites →https://doi.org/10.1016/j.molcel.2015.01.018openalex-snapshot
Limited Mitochondrial Permeabilization Causes DNA Damage and Genomic Instability in the Absence of Cell Death
inferredcites →https://doi.org/10.1016/j.molmet.2013.11.005openalex-snapshot
Identification of a novel mitochondrial uncoupler that does not depolarize the plasma membrane
inferredcites →https://doi.org/10.1016/j.molmet.2021.101222openalex-snapshot
Exploring the therapeutic potential of mitochondrial uncouplers in cancer
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.08.002openalex-snapshot
Control of OXPHOS efficiency by complex I in brain mitochondria
inferredcites →https://doi.org/10.1016/j.phrs.2022.106356openalex-snapshot
Pharmacological senolysis reduces doxorubicin-induced cardiotoxicity and improves cardiac function in mice
inferredcites →https://doi.org/10.1016/j.redox.2020.101606openalex-snapshot
Mitochondria-targeted paraquat and metformin mediate ROS production to induce multiple pathways of retrograde signaling: A dose-dependent phenomenon
inferredcites →https://doi.org/10.1016/j.semcancer.2020.09.012openalex-snapshot
Mitochondrial mutations and mitoepigenetics: Focus on regulation of oxidative stress-induced responses in breast cancers
inferredcites →https://doi.org/10.1016/j.tips.2012.03.010openalex-snapshot
Mitochondrial pharmacology
inferredcites →https://doi.org/10.1016/s0021-9258(19)50355-6openalex-snapshot
Modulation of the mitochondrial cyclosporin A-sensitive permeability transition pore by the proton electrochemical gradient. Evidence that the pore can be opened by membrane depolarization.
inferredcites →https://doi.org/10.1016/s1470-2045(10)70261-8openalex-snapshot
Navitoclax, a targeted high-affinity inhibitor of BCL-2, in lymphoid malignancies: a phase 1 dose-escalation study of safety, pharmacokinetics, pharmacodynamics, and antitumour activity
inferredcites →https://doi.org/10.1021/acs.jmedchem.7b01182openalex-snapshot
Small Molecule Mitochondrial Uncouplers and Their Therapeutic Potential
inferredcites →https://doi.org/10.1023/a:1022945107762openalex-snapshot
The mitochondrial membrane potential (Δψm) in apoptosis; an update
inferredcites →https://doi.org/10.1023/a:1026331226241openalex-snapshot
Effect of Metabolic Inhibitors on Membrane Potential and Ion Conductance of Rat Astrocytes
inferredcites →https://doi.org/10.1038/228562a0openalex-snapshot
Unexpected Features of the Action of Dinitrophenol on Cortical Neurones
inferredcites →https://doi.org/10.1038/cdd.2017.179openalex-snapshot
MOMP, cell suicide as a BCL-2 family business
inferredcites →https://doi.org/10.1038/msb.2010.5openalex-snapshot
Feedback between p21 and reactive oxygen production is necessary for cell senescence
inferredcites →https://doi.org/10.1038/ncomms4837openalex-snapshot
Low abundance of the matrix arm of complex I in mitochondria predicts longevity in mice
inferredcites →https://doi.org/10.1038/nm.4010openalex-snapshot
Clearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
inferredcites →https://doi.org/10.1038/s41418-018-0118-3openalex-snapshot
Selective elimination of senescent cells by mitochondrial targeting is regulated by ANT2
inferredcites →https://doi.org/10.1038/s41419-020-03074-9openalex-snapshot
Cellular senescence contributes to radiation-induced hyposalivation by affecting the stem/progenitor cell niche
inferredcites →https://doi.org/10.1038/s41467-020-16298-2openalex-snapshot
Mitochondrial uncoupler BAM15 reverses diet-induced obesity and insulin resistance in mice
inferredcites →https://doi.org/10.1038/s41467-020-18714-zopenalex-snapshot
Author Correction: Identification and characterization of Cardiac Glycosides as senolytic compounds
inferredcites →https://doi.org/10.1038/s41467-022-29824-1openalex-snapshot
Single-cell transcriptomics identifies Mcl-1 as a target for senolytic therapy in cancer
inferredcites →https://doi.org/10.1038/s41467-022-35657-9openalex-snapshot
Targeting anti-apoptotic pathways eliminates senescent melanocytes and leads to nevi regression
inferredcites →https://doi.org/10.1038/s41586-018-0543-yopenalex-snapshot
Clearance of senescent glial cells prevents tau-dependent pathology and cognitive decline
inferredcites →https://doi.org/10.1038/s41591-022-01923-yopenalex-snapshot
Cellular senescence and senolytics: the path to the clinic
inferredcites →https://doi.org/10.1038/sj.cdd.4402091openalex-snapshot
Failure of stress-induced downregulation of Bcl-2 contributes to apoptosis resistance in senescent human diploid fibroblasts
inferredcites →https://doi.org/10.1042/bcj20210608openalex-snapshot
BH3 mimetics and TKI combined therapy for Chronic Myeloid Leukemia
inferredcites →https://doi.org/10.1042/bj20040095openalex-snapshot
Senescence-associated changes in respiration and oxidative phosphorylation in primary human fibroblasts
inferredcites →https://doi.org/10.1046/j.1474-9728.2003.00040.xopenalex-snapshot
MitoQ counteracts telomere shortening and elongates lifespan of fibroblasts under mild oxidative stress
inferredcites →https://doi.org/10.1073/pnas.92.20.9363openalex-snapshot
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
inferredcites →https://doi.org/10.1074/jbc.m404003200openalex-snapshot
Supplementation of Endothelial Cells with Mitochondria-targeted Antioxidants Inhibit Peroxide-induced Mitochondrial Iron Uptake, Oxidative Damage, and Apoptosis
inferredcites →https://doi.org/10.1080/10428194.2020.1845332openalex-snapshot
Safety and efficacy of navitoclax, a BCL-2 and BCL-X L inhibitor, in patients with relapsed or refractory lymphoid malignancies: results from a phase 2a study
inferredcites →https://doi.org/10.1089/ars.2011.3969openalex-snapshot
Mitochondria-Targeted Small Molecule Therapeutics and Probes
inferredcites →https://doi.org/10.1093/bioinformatics/btw230openalex-snapshot
Combenefit: an interactive platform for the analysis and visualization of drug combinations
inferredcites →https://doi.org/10.1093/gerona/glt136openalex-snapshot
A Clinical Frailty Index in Aging Mice: Comparisons With Frailty Index Data in Humans
inferredcites →https://doi.org/10.1093/jnci/djq364openalex-snapshot
Therapy-Induced Senescence in Cancer
inferredcites →https://doi.org/10.1093/lifemedi/lnac030openalex-snapshot
Targeting senescent cells for a healthier longevity: the roadmap for an era of global aging
inferredcites →https://doi.org/10.1093/toxsci/kfm052openalex-snapshot
Circumventing the Crabtree Effect: Replacing Media Glucose with Galactose Increases Susceptibility of HepG2 Cells to Mitochondrial Toxicants
inferredcites →https://doi.org/10.1098/rsfs.2016.0109openalex-snapshot
Mitochondria-targeted metformins: anti-tumour and redox signalling mechanisms
inferredcites →https://doi.org/10.1111/acel.12344openalex-snapshot
The Achilles’ heel of senescent cells: from transcriptome to senolytic drugs
inferredcites →https://doi.org/10.1111/acel.12445openalex-snapshot
Identification of a novel senolytic agent, navitoclax, targeting the Bcl‐2 family of anti‐apoptotic factors
inferredcites →https://doi.org/10.1111/acel.12945openalex-snapshot
Pharmacological clearance of senescent cells improves survival and recovery in aged mice following acute myocardial infarction
inferredcites →https://doi.org/10.1111/acel.13188openalex-snapshot
Anti‐inflammatory treatment rescues memory deficits during aging in nfkb1−/− mice
inferredcites →https://doi.org/10.1111/acel.13817openalex-snapshot
Effect of peripheral cellular senescence on brain aging and cognitive decline
inferredcites →https://doi.org/10.1111/hepr.13879openalex-snapshot
Navitoclax improves acute‐on‐chronic liver failure by eliminating senescent cells in mice
inferredcites →https://doi.org/10.1111/j.1469-7793.1998.819ba.xopenalex-snapshot
Effects of mitochondrial uncouplers on intracellular calcium, pH and membrane potential in rat carotid body type I cells
inferredcites →https://doi.org/10.1111/joim.13141openalex-snapshot
Senolytic drugs: from discovery to translation
inferredcites →https://doi.org/10.1126/scitranslmed.abb0203openalex-snapshot
Cellular senescence inhibits renal regeneration after injury in mice, with senolytic treatment promoting repair
inferredcites →https://doi.org/10.1128/mcb.01868-08openalex-snapshot
Mitochondrial Dysfunction Contributes to Oncogene-Induced Senescence
inferredcites →https://doi.org/10.1158/0008-5472.can-07-5836openalex-snapshot
ABT-263: A Potent and Orally Bioavailable Bcl-2 Family Inhibitor
inferredcites →https://doi.org/10.1161/circulationaha.122.058794openalex-snapshot
Eliminating Senescent Cells Can Promote Pulmonary Hypertension Development and Progression
inferredcites →https://doi.org/10.1172/jci158447openalex-snapshot
Mitochondrial dysfunction in cell senescence and aging
inferredcites →https://doi.org/10.1172/jci162519openalex-snapshot
Local senolysis in aged mice only partially replicates the benefits of systemic senolysis
inferredcites →https://doi.org/10.1182/blood-2011-04-347849openalex-snapshot
Bcl-xL–inhibitory BH3 mimetics can induce a transient thrombocytopathy that undermines the hemostatic function of platelets
inferredcites →https://doi.org/10.1186/2046-2395-1-3openalex-snapshot
Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction
inferredcites →https://doi.org/10.1242/jcs.059246openalex-snapshot
Decreased expression of Drp1 and Fis1 mediates mitochondrial elongation in senescent cells and enhances resistance to oxidative stress through PINK1
inferredcites →https://doi.org/10.12688/f1000research.9629.1openalex-snapshot
Mitochondrial apoptosis and BH3 mimetics
inferredcites →https://doi.org/10.1371/journal.pbio.0050110openalex-snapshot
Mitochondrial Dysfunction Accounts for the Stochastic Heterogeneity in Telomere-Dependent Senescence
inferredcites →https://doi.org/10.1371/journal.pcbi.1003728openalex-snapshot
Dynamic Modelling of Pathways to Cellular Senescence Reveals Strategies for Targeted Interventions
inferredcites →https://doi.org/10.15252/embj.201592862openalex-snapshot
Mitochondria are required for pro‐ageing features of the senescent phenotype
inferredcites →https://doi.org/10.15252/emmm.202012088openalex-snapshot
BAM15‐mediated mitochondrial uncoupling protects against obesity and improves glycemic control
inferredcites →https://doi.org/10.18632/aging.100196openalex-snapshot
Adult-onset, short-term dietary restriction reduces cell senescence in mice
inferredcites →https://doi.org/10.18632/aging.101202openalex-snapshot
New agents that target senescent cells: the flavone, fisetin, and the BCL-XL inhibitors, A1331852 and A1155463
inferredcites →https://doi.org/10.3389/fcell.2020.00354openalex-snapshot
The Senolytic Drug Navitoclax (ABT-263) Causes Trabecular Bone Loss and Impaired Osteoprogenitor Function in Aged Mice
inferredcites →https://doi.org/10.3390/cancers12040822openalex-snapshot
Therapy-Induced Senescence: An “Old” Friend Becomes the Enemy
inferredcites →https://doi.org/10.3892/ijo.26.4.1069openalex-snapshot
Uncoupling of oxidative phosphorylation and Smac/DIABLO release are not sufficient to account for induction of apoptosis by sulindac sulfide in human colorectal cancer cells
inferredcites →https://doi.org/10.4103/0976-0105.177703openalex-snapshot
A simple practice guide for dose conversion between animals and human
inferredcites →https://doi.org/10.7554/elife.75492openalex-snapshot
Short senolytic or senostatic interventions rescue progression of radiation-induced frailty and premature ageing in mice

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

inferred← citeshttps://doi.org/10.1016/j.arr.2024.102558openalex-snapshot
Oxidative stress and cell senescence as drivers of ageing: Chicken and egg
inferred← citeshttps://doi.org/10.1016/j.mad.2023.111888openalex-snapshot
Current senolytics: Mode of action, efficacy and limitations, and their future
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