On the public citation graph
Why cancer cells have a more hyperpolarised mitochondrial membrane potential and emergent prospects for therapy
0 signed · 219 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/biof.31openalex-snapshot
The bioenergetics of cancer: Is glycolysis the main ATP supplier in all tumor cells?
inferredcites →https://doi.org/10.1002/cbic.201300115openalex-snapshot
A Prototypical Small‐Molecule Modulator Uncouples Mitochondria in Response to Endogenous Hydrogen Peroxide Production
inferredcites →https://doi.org/10.1002/jnr.22659openalex-snapshot
The “B Space” of mitochondrial phosphorylation
inferredcites →https://doi.org/10.1007/s00249-013-0898-9openalex-snapshot
Electrogenic proton transport across lipid bilayer membranes mediated by cationic derivatives of rhodamine 19: comparison with anionic protonophores
inferredcites →https://doi.org/10.1007/s10540-006-9018-8openalex-snapshot
Targeting Dinitrophenol to Mitochondria: Limitations to the Development of a Self-limiting Mitochondrial Protonophore
inferredcites →https://doi.org/10.1007/s10637-015-0221-yopenalex-snapshot
A phase I open-labeled, single-arm, dose-escalation, study of dichloroacetate (DCA) in patients with advanced solid tumors
inferredcites →https://doi.org/10.1007/s10863-005-8642-5openalex-snapshot
ANT2 Isoform Required for Cancer Cell Glycolysis
inferredcites →https://doi.org/10.1007/s13181-011-0162-6openalex-snapshot
2,4-Dinitrophenol (DNP): A Weight Loss Agent with Significant Acute Toxicity and Risk of Death
inferredcites →https://doi.org/10.1016/0006-291x(84)91453-0openalex-snapshot
Rhodamine 123 inhibits bioenergetic function in isolated rat liver mitochondria
inferredcites →https://doi.org/10.1016/0006-291x(90)90861-gopenalex-snapshot
A single amino acid substitution in lactate dehydrogenase improves the catalytic efficiency with an alternative coenzyme
inferredcites →https://doi.org/10.1016/j.bbabio.2007.05.010openalex-snapshot
Effects of lipophilic dications on planar bilayer phospholipid membrane and mitochondria
inferredcites →https://doi.org/10.1016/j.bbabio.2010.03.025openalex-snapshot
The pivotal roles of mitochondria in cancer: Warburg and beyond and encouraging prospects for effective therapies
inferredcites →https://doi.org/10.1016/j.bbabio.2010.08.010openalex-snapshot
The Warburg and Crabtree effects: On the origin of cancer cell energy metabolism and of yeast glucose repression
inferredcites →https://doi.org/10.1016/j.bbabio.2010.10.008openalex-snapshot
Adenine nucleotide translocase 2 is a key mitochondrial protein in cancer metabolism
inferredcites →https://doi.org/10.1016/j.bbadis.2009.08.008openalex-snapshot
Mitochondria as ATP consumers in cellular pathology
inferredcites →https://doi.org/10.1016/j.bbamem.2008.04.011openalex-snapshot
The ADP and ATP transport in mitochondria and its carrier
inferredcites →https://doi.org/10.1016/j.bbrc.2007.07.165openalex-snapshot
Mixed lineage kinase 3 connects reactive oxygen species to c-Jun NH2-terminal kinase-induced mitochondrial apoptosis in genipin-treated PC3 human prostate cancer cells
inferredcites →https://doi.org/10.1016/j.bcp.2005.07.025openalex-snapshot
Genipin-induced apoptosis in hepatoma cells is mediated by reactive oxygen species/c-Jun NH2-terminal kinase-dependent activation of mitochondrial pathway
inferredcites →https://doi.org/10.1016/j.biocel.2008.06.013openalex-snapshot
Energetic signalling in the control of mitochondrial F1F0 ATP synthase activity in health and disease
inferredcites →https://doi.org/10.1016/j.biocel.2013.06.023openalex-snapshot
Nigericin selectively targets cancer stem cells in nasopharyngeal carcinoma
inferredcites →https://doi.org/10.1016/j.bpj.2012.08.050openalex-snapshot
A Biophysical Model of the Mitochondrial ATP-Mg/Pi Carrier
inferredcites →https://doi.org/10.1016/j.bpj.2012.11.1689openalex-snapshot
Translocation of Glycolytic ATP into Mitochondria of Cancer Cells does not Utilize the Adenine Nucleotide Transporter
inferredcites →https://doi.org/10.1016/j.cbi.2014.01.015openalex-snapshot
Clusianone, a naturally occurring nemorosone regioisomer, uncouples rat liver mitochondria and induces HepG2 cell death
inferredcites →https://doi.org/10.1016/j.ccr.2006.04.023openalex-snapshot
Attenuation of LDH-A expression uncovers a link between glycolysis, mitochondrial physiology, and tumor maintenance
inferredcites →https://doi.org/10.1016/j.ccr.2006.10.020openalex-snapshot
A Mitochondria-K+ Channel Axis Is Suppressed in Cancer and Its Normalization Promotes Apoptosis and Inhibits Cancer Growth
inferredcites →https://doi.org/10.1016/j.cell.2010.11.010openalex-snapshot
ATP Consumption Promotes Cancer Metabolism
inferredcites →https://doi.org/10.1016/j.cmet.2007.10.002openalex-snapshot
The Biology of Cancer: Metabolic Reprogramming Fuels Cell Growth and Proliferation
inferredcites →https://doi.org/10.1016/j.febslet.2011.04.004openalex-snapshot
Mitochondrial consumption of cytosolic ATP: Not so fast
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2010.05.031openalex-snapshot
Uncoupling protein-2 knockdown mediates the cytotoxic effects of cisplatin
inferredcites →https://doi.org/10.1016/j.jphotobiol.2008.12.010openalex-snapshot
Two-photon autofluorescence dynamics imaging reveals sensitivity of intracellular NADH concentration and conformation to cell physiology at the single-cell level
inferredcites →https://doi.org/10.1016/j.mam.2012.05.006openalex-snapshot
The mitochondrial ADP/ATP carrier (SLC25 family): Pathological implications of its dysfunction
inferredcites →https://doi.org/10.1016/j.mehy.2014.05.001openalex-snapshot
A new model for mitochondrial membrane potential production and storage
inferredcites →https://doi.org/10.1016/j.mito.2009.12.143openalex-snapshot
Uncoupling protein-2 and cancer
inferredcites →https://doi.org/10.1016/j.mito.2010.10.008openalex-snapshot
The anti-cancer agent nemorosone is a new potent protonophoric mitochondrial uncoupler
inferredcites →https://doi.org/10.1016/j.mito.2014.09.002openalex-snapshot
ATP/ADP ratio, the missed connection between mitochondria and the Warburg effect
inferredcites →https://doi.org/10.1016/j.phymed.2011.10.008openalex-snapshot
Effects of (−) mammea A/BB isolated from Calophyllum brasiliense leaves and derivatives on mitochondrial membrane of Leishmania amazonensis
inferredcites →https://doi.org/10.1016/j.tiv.2007.12.005openalex-snapshot
2,4-Dinitrophenol induces G1 phase arrest and apoptosis in human pulmonary adenocarcinoma Calu-6 cells
inferredcites →https://doi.org/10.1016/j.yexmp.2010.08.006openalex-snapshot
Cancer metabolism: The Warburg effect today
inferredcites →https://doi.org/10.1016/s0014-5793(04)00242-xopenalex-snapshot
The role and structure of mitochondrial carriers
inferredcites →https://doi.org/10.1016/s0014-5793(04)00293-5openalex-snapshot
Adenine nucleotide translocase 3 (ANT3) overexpression induces apoptosis in cultured cells
inferredcites →https://doi.org/10.1016/s0021-9258(17)38802-6openalex-snapshot
Mitochondrial and plasma membrane potentials cause unusual accumulation and retention of rhodamine 123 by human breast adenocarcinoma-derived MCF-7 cells.
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1016/s0026-895x(24)12222-5openalex-snapshot
Further Insight into Mechanism of Action of Clodronate: Inhibition of Mitochondrial ADP/ATP Translocase by a Nonhydrolyzable, Adenine-Containing Metabolite
inferredcites →https://doi.org/10.1016/s0169-409x(01)00125-9openalex-snapshot
Delocalized lipophilic cations selectively target the mitochondria of carcinoma cells
inferredcites →https://doi.org/10.1016/s0169-409x(01)00131-4openalex-snapshot
Cationic bolasomes with delocalized charge centers as mitochondria-specific DNA delivery systems
inferredcites →https://doi.org/10.1016/s0169-409x(99)00069-1openalex-snapshot
Drug delivery to mitochondria: the key to mitochondrial medicine
inferredcites →https://doi.org/10.1016/s0531-5565(00)00135-2openalex-snapshot
Uncoupling to survive? The role of mitochondrial inefficiency in ageing
inferredcites →https://doi.org/10.1016/s0939-6411(03)00046-8openalex-snapshot
Hyperforin a constituent of St John's wort (Hypericum perforatum L.) extract induces apoptosis by triggering activation of caspases and with hypericin synergistically exerts cytotoxicity towards human malignant cell lines
inferredcites →https://doi.org/10.1016/s1535-6108(02)00082-xopenalex-snapshot
A novel mitochondriotoxic small molecule that selectively inhibits tumor cell growth
inferredcites →https://doi.org/10.1021/bi0261490openalex-snapshot
The Human Mitochondrial ADP/ATP Carriers: Kinetic Properties and Biogenesis of Wild-Type and Mutant Proteins in the YeastS. cerevisiae
inferredcites →https://doi.org/10.1021/cb400944yopenalex-snapshot
Mito-DCA: A Mitochondria Targeted Molecular Scaffold for Efficacious Delivery of Metabolic Modulator Dichloroacetate
inferredcites →https://doi.org/10.1021/jm0509039openalex-snapshot
Immuno-suppressive Effect of Blocking the CD28 Signaling Pathway in T-cells by an Active Component of Echinacea Found by a Novel Pharmaceutical Screening Method
inferredcites →https://doi.org/10.1021/jm500174vopenalex-snapshot
Antiproliferative and Uncoupling Effects of Delocalized, Lipophilic, Cationic Gallic Acid Derivatives on Cancer Cell Lines. Validation in Vivo in Singenic Mice
inferredcites →https://doi.org/10.1021/mp900032ropenalex-snapshot
Multiple Triphenylphosphonium Cations Shuttle a Hydrophilic Peptide into Mitochondria
inferredcites →https://doi.org/10.1021/np100501nopenalex-snapshot
Mammea E/BB, an Isoprenylated Dihydroxycoumarin Protonophore That Potently Uncouples Mitochondrial Electron Transport, Disrupts Hypoxic Signaling in Tumor Cells
inferredcites →https://doi.org/10.1021/np300711eopenalex-snapshot
Glycolysis Inhibitor Screening Identifies the Bis-geranylacylphloroglucinol Protonophore Moronone from Moronobea coccinea
inferredcites →https://doi.org/10.1023/a:1008336904585openalex-snapshot
Phase I trial of the selective mitochondrial toxin MKT 077 in chemo-resistant solid tumours
inferredcites →https://doi.org/10.1038/35048073openalex-snapshot
The mitochondrion in apoptosis: how Pandora's box opens
inferredcites →https://doi.org/10.1038/415096aopenalex-snapshot
Superoxide activates mitochondrial uncoupling proteins
inferredcites →https://doi.org/10.1038/446474aopenalex-snapshot
Cancer patients opt for unapproved drug
inferredcites →https://doi.org/10.1038/emboj.2011.401openalex-snapshot
UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells
inferredcites →https://doi.org/10.1038/nature02056openalex-snapshot
Structure of mitochondrial ADP/ATP carrier in complex with carboxyatractyloside
inferredcites →https://doi.org/10.1038/nature02229openalex-snapshot
The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore
inferredcites →https://doi.org/10.1038/nature06734openalex-snapshot
The M2 splice isoform of pyruvate kinase is important for cancer metabolism and tumour growth
inferredcites →https://doi.org/10.1038/nature06903openalex-snapshot
A novel route for ATP acquisition by the remnant mitochondria of Encephalitozoon cuniculi
inferredcites →https://doi.org/10.1038/nature08882openalex-snapshot
Zscan4 regulates telomere elongation and genomic stability in ES cells
inferredcites →https://doi.org/10.1038/nature13110openalex-snapshot
Metabolic determinants of cancer cell sensitivity to glucose limitation and biguanides
inferredcites →https://doi.org/10.1038/ncomms4936openalex-snapshot
Separating NADH and NADPH fluorescence in live cells and tissues using FLIM
inferredcites →https://doi.org/10.1038/ncpcardio0766openalex-snapshot
Mitochondrial oxidative metabolism is required for the cardiac differentiation of stem cells
inferredcites →https://doi.org/10.1038/nrc1478openalex-snapshot
Why do cancers have high aerobic glycolysis?
inferredcites →https://doi.org/10.1038/nrm2820openalex-snapshot
Sensors and regulators of intracellular pH
inferredcites →https://doi.org/10.1038/sj.bjp.0706628openalex-snapshot
A new endogenous ATP analog (ApppI) inhibits the mitochondrial adenine nucleotide translocase (ANT) and is responsible for the apoptosis induced by nitrogen‐containing bisphosphonates
inferredcites →https://doi.org/10.1038/stemcells.2008.62openalex-snapshot
Cancer and embryonic stem cells share genetic fingerprints
inferredcites →https://doi.org/10.1042/bj20050890openalex-snapshot
The basal proton conductance of mitochondria depends on adenine nucleotide translocase content
inferredcites →https://doi.org/10.1042/bj20060706openalex-snapshot
Carboxyatractyloside effects on brown-fat mitochondria imply that the adenine nucleotide translocator isoforms ANT1 and ANT2 may be responsible for basal and fatty-acid-induced uncoupling respectively
inferredcites →https://doi.org/10.1042/bj20060919openalex-snapshot
Accumulation of lipophilic dications by mitochondria and cells
inferredcites →https://doi.org/10.1042/bj20070606openalex-snapshot
Mitochondrial uncouplers with an extraordinary dynamic range
inferredcites →https://doi.org/10.1046/j.1467-789x.2001.00043.xopenalex-snapshot
Mitochondrial uncoupling as a target for drug development for the treatment of obesity
inferredcites →https://doi.org/10.1073/pnas.0401346101openalex-snapshot
Restoration of an absent G 1 arrest and protection from apoptosis in embryonic stem cells after ionizing radiation
inferredcites →https://doi.org/10.1073/pnas.1011099107openalex-snapshot
Bioenergetic cost of making an adenosine triphosphate molecule in animal mitochondria
inferredcites →https://doi.org/10.1073/pnas.1103621108openalex-snapshot
Macromolecular organization of ATP synthase and complex I in whole mitochondria
inferredcites →https://doi.org/10.1073/pnas.1317400111openalex-snapshot
UCP2 transports C4 metabolites out of mitochondria, regulating glucose and glutamine oxidation
inferredcites →https://doi.org/10.1073/pnas.79.17.5292openalex-snapshot
Unusual retention of rhodamine 123 by mitochondria in muscle and carcinoma cells.
inferredcites →https://doi.org/10.1073/pnas.84.15.5444openalex-snapshot
Dequalinium, a topical antimicrobial agent, displays anticarcinoma activity based on selective mitochondrial accumulation.
inferredcites →https://doi.org/10.1074/jbc.m114.568204openalex-snapshot
The Chemical Uncoupler 2,4-Dinitrophenol (DNP) Protects against Diet-induced Obesity and Improves Energy Homeostasis in Mice at Thermoneutrality
inferredcites →https://doi.org/10.1074/jbc.m510916200openalex-snapshot
Simultaneous Monitoring of Ionophore- and Inhibitor-mediated Plasma and Mitochondrial Membrane Potential Changes in Cultured Neurons
inferredcites →https://doi.org/10.1074/jbc.m511064200openalex-snapshot
Induction of Oxidative Metabolism by Mitochondrial Frataxin Inhibits Cancer Growth
inferredcites →https://doi.org/10.1074/jbc.m806903200openalex-snapshot
Nonmitochondrial ATP/ADP Transporters Accept Phosphate as Third Substrate
inferredcites →https://doi.org/10.1083/jcb.147.7.1493openalex-snapshot
Adenine Nucleotide Translocase-1, a Component of the Permeability Transition Pore, Can Dominantly Induce Apoptosis
inferredcites →https://doi.org/10.1089/ars.2014.5952openalex-snapshot
Molecular Strategies for Targeting Antioxidants to Mitochondria: Therapeutic Implications
inferredcites →https://doi.org/10.1093/abbs/gmq063openalex-snapshot
Mitochondrial F1Fo-ATP synthase translocates to cell surface in hepatocytes and has high activity in tumor-like acidic and hypoxic environment
inferredcites →https://doi.org/10.1093/annonc/mdu331.38openalex-snapshot
A Phase I Open-Labelled, Single-Arm, Dose-Escalation, Study of Dichloroacetate (Dca) in Patients with Advanced Solid Tumours
inferredcites →https://doi.org/10.1096/fj.09-149898openalex-snapshot
Forward operation of adenine nucleotide translocase during F 0 F 1 ‐ATPase reversal: critical role of matrix substrate‐level phosphorylation
inferredcites →https://doi.org/10.1096/fj.10-162222openalex-snapshot
Mitochondrial matrix pH controls oxidative phosphorylation and metabolism‐secretion coupling in INS‐1E clonal β cells
inferredcites →https://doi.org/10.1097/00005392-199909010-00090openalex-snapshot
CALCIUM IONOPHORE, IONOMYCIN INHIBITS GROWTH OF HUMAN BLADDER CANCER CELLS BOTH IN VITRO AND IN VIVO WITH ALTERATION OF BCL-2 AND BAX EXPRESSION LEVELS
inferredcites →https://doi.org/10.1097/nen.0b013e3181b40217openalex-snapshot
Peripheral Neuropathy in Rats Exposed to Dichloroacetate
inferredcites →https://doi.org/10.1111/bph.12638openalex-snapshot
The compound BTB 06584 is an IF 1‐dependent selective inhibitor of the mitochondrial F 1 F o‐ ATP ase
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06300.xopenalex-snapshot
Yeast mitochondria import ATP through the calcium‐dependent ATP‐Mg/Pi carrier Sal1p, and are ATP consumers during aerobic growth in glucose
inferredcites →https://doi.org/10.1111/j.1432-1033.1977.tb11625.xopenalex-snapshot
The Adenine-Nucleotide Exchange in Submitochondrial (Sonic) Particles
inferredcites →https://doi.org/10.1111/j.1742-4658.2010.07702.xopenalex-snapshot
The silencing of adenine nucleotide translocase isoform 1 induces oxidative stress and programmed cell death in ADF human glioblastoma cells
inferredcites →https://doi.org/10.1111/j.1755-5922.2008.00065.xopenalex-snapshot
Pharmacological Profile of the Selective Mitochondrial F 1 F 0 ATP Hydrolase Inhibitor BMS‐199264 in Myocardial Ischemia
inferredcites →https://doi.org/10.1126/science.1160809openalex-snapshot
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
inferredcites →https://doi.org/10.1126/science.123.3191.309openalex-snapshot
On the Origin of Cancer Cells
inferredcites →https://doi.org/10.1126/science.7146897openalex-snapshot
Rhodamine-123 Selectively Reduces Clonal Growth of Carcinoma Cells in Vitro
inferredcites →https://doi.org/10.1126/scitranslmed.3000677openalex-snapshot
Metabolic Modulation of Glioblastoma with Dichloroacetate
inferredcites →https://doi.org/10.1128/jb.00371-06openalex-snapshot
Study of the Five Rickettsia prowazekii Proteins Annotated as ATP/ADP Translocases (Tlc): Only Tlc1 Transports ATP/ADP, While Tlc4 and Tlc5 Transport Other Ribonucleotides
inferredcites →https://doi.org/10.1128/jb.00391-08openalex-snapshot
Lawsonia intracellularis Contains a Gene Encoding a Functional Rickettsia-Like ATP/ADP Translocase for Host Exploitation
inferredcites →https://doi.org/10.1128/jb.186.3.683-691.2004openalex-snapshot
ATP/ADP Translocases: a Common Feature of Obligate Intracellular Amoebal Symbionts Related to Chlamydiae and Rickettsiae
inferredcites →https://doi.org/10.1128/mmbr.00016-08openalex-snapshot
ATP Synthase and the Actions of Inhibitors Utilized To Study Its Roles in Human Health, Disease, and Other Scientific Areas
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154237openalex-snapshot
Aerobic Glycolysis: Meeting the Metabolic Requirements of Cell Proliferation
inferredcites →https://doi.org/10.1146/annurev.cb.04.110188.001103openalex-snapshot
Mitochondrial Membrane Potential in Living Cells
inferredcites →https://doi.org/10.1146/annurev.cellbio.4.1.155openalex-snapshot
Mitochondrial Membrane Potential In Living Cells
inferredcites →https://doi.org/10.1146/annurev.med.53.082901.104028openalex-snapshot
Positron Emission Tomography Scanning: Current and Future Applications
inferredcites →https://doi.org/10.1152/ajpheart.01019.2003openalex-snapshot
Excessive ATP hydrolysis in ischemic myocardium by mitochondrial F1F0-ATPase: effect of selective pharmacological inhibition of mitochondrial ATPase hydrolase activity
inferredcites →https://doi.org/10.1152/physiol.00005.2006openalex-snapshot
Molecular, Functional, and Pathological Aspects of the Mitochondrial ADP/ATP Carrier
inferredcites →https://doi.org/10.1155/2011/978583openalex-snapshot
Stable Differences in Intrinsic Mitochondrial Membrane Potential of Tumor Cell Subpopulations Reflect Phenotypic Heterogeneity
inferredcites →https://doi.org/10.1158/0008-5472.can-05-2444openalex-snapshot
The Intrinsic Mitochondrial Membrane Potential of Colonic Carcinoma Cells Is Linked to the Probability of Tumor Progression
inferredcites →https://doi.org/10.1158/0008-5472.can-05-2717openalex-snapshot
Growth Properties of Colonic Tumor Cells Are a Function of the Intrinsic Mitochondrial Membrane Potential
inferredcites →https://doi.org/10.1158/0008-5472.can-05-4407openalex-snapshot
Chemosensitization by Knockdown of Adenine Nucleotide Translocase-2
inferredcites →https://doi.org/10.1158/0008-5472.can-06-1501openalex-snapshot
Cancer's Molecular Sweet Tooth and the Warburg Effect
inferredcites →https://doi.org/10.1158/0008-5472.can-08-0053openalex-snapshot
The Mitochondrial Uncoupling Protein-2 Promotes Chemoresistance in Cancer Cells
inferredcites →https://doi.org/10.1158/0008-5472.can-08-0555openalex-snapshot
The Warburg Effect in Leukemia-Stroma Cocultures Is Mediated by Mitochondrial Uncoupling Associated with Uncoupling Protein 2 Activation
inferredcites →https://doi.org/10.1158/1535-7163.mct-06-0024openalex-snapshot
Tumor pH controls the in vivo efficacy of weak acid and base chemotherapeutics
inferredcites →https://doi.org/10.1186/1471-2407-8-160openalex-snapshot
Over-expression of Adenine Nucleotide Translocase 1 (ANT1) Induces Apoptosis and Tumor Regression in vivo
inferredcites →https://doi.org/10.1186/1476-4598-12-152openalex-snapshot
Tumor glycolysis as a target for cancer therapy: progress and prospects
inferredcites →https://doi.org/10.1186/bcr1857openalex-snapshot
Suppression of adenine nucleotide translocase-2 by vector-based siRNA in human breast cancer cells induces apoptosis and inhibits tumor growth in vitro and in vivo
inferredcites →https://doi.org/10.1211/jpp.59.5.0013openalex-snapshot
Antiproliferative, cytotoxic and antitumour activity of coumarins isolated from Calophyllum brasiliense
inferredcites →https://doi.org/10.1242/jeb.203.1.41openalex-snapshot
Steady-State and Pre-Steady-State Kinetics of the Mitochondrial F1Fo ATPase: Is Atp Synthase a Reversible Molecular Machine?
inferredcites →https://doi.org/10.1248/bpb.29.817openalex-snapshot
Selective Cytotoxic Activity of Valinomycin against HT-29 Human Colon Carcinoma Cells via Down-Regulation of GRP78
inferredcites →https://doi.org/10.1289/ehp.9087213openalex-snapshot
Uncouplers of Oxidative Phosphorylation
inferredcites →https://doi.org/10.1371/journal.pbio.0050231openalex-snapshot
Enlightening Energy Parasitism by Analysis of an ATP/ADP Transporter from Chlamydiae
inferredcites →https://doi.org/10.1371/journal.pone.0013289openalex-snapshot
Genipin-Induced Inhibition of Uncoupling Protein-2 Sensitizes Drug-Resistant Cancer Cells to Cytotoxic Agents
inferredcites →https://doi.org/10.1371/journal.pone.0018433openalex-snapshot
Mild Mitochondrial Uncoupling and Calorie Restriction Increase Fasting eNOS, Akt and Mitochondrial Biogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0024792openalex-snapshot
Cellular Model of Warburg Effect Identifies Tumor Promoting Function of UCP2 in Breast Cancer and Its Suppression by Genipin
inferredcites →https://doi.org/10.1371/journal.pone.0030714openalex-snapshot
UCP2 Inhibits ROS-Mediated Apoptosis in A549 under Hypoxic Conditions
inferredcites →https://doi.org/10.1371/journal.pone.0061902openalex-snapshot
Penetrating Cations Enhance Uncoupling Activity of Anionic Protonophores in Mitochondria
inferredcites →https://doi.org/10.1371/journal.pone.0109174openalex-snapshot
Inhibition Effect of a Custom Peptide on Lung Tumors
inferredcites →https://doi.org/10.14670/hh-22.85openalex-snapshot
Protection from oxidative stress by enhanced glycolysis; a possible mechanism of cellular immortalization.
inferredcites →https://doi.org/10.15252/embj.201490446openalex-snapshot
Pluripotent stem cell energy metabolism: an update
inferredcites →https://doi.org/10.2174/1381612819666131230124334openalex-snapshot
ATP Synthesis Revisited: New Avenues for the Management of Mitochondrial Diseases
inferredcites →https://doi.org/10.2174/187152008783961932openalex-snapshot
The Warburg Effect: Why and How Do Cancer Cells Activate Glycolysis in the Presence of Oxygen?
inferredcites →https://doi.org/10.3389/fphys.2013.00370openalex-snapshot
pH sensing and regulation in cancer
inferredcites →https://doi.org/10.3390/cancers2020567openalex-snapshot
Role of Uncoupling Proteins in Cancer
inferredcites →https://doi.org/10.3748/wjg.v21.i11.3232openalex-snapshot
Mitochondrial uncoupling protein 2 and pancreatic cancer: A new potential target therapy
inferredcites →https://doi.org/10.4236/jct.2014.53036openalex-snapshot
Want to Cure Cancer? Then Revisit the Past; “Warburg Was Correct”, Cancer Is a Metabolic Disease
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adma.202209529openalex-snapshot
In Response to Precision Medicine: Current Subcellular Targeting Strategies for Cancer Therapy
inferred← citeshttps://doi.org/10.1002/glia.23905openalex-snapshot
Mitochondrial dynamics and bioenergetics regulated by netrin‐1 in oligodendrocytes
inferred← citeshttps://doi.org/10.1007/978-1-0716-2309-1_11openalex-snapshot
Mitochondrial Toxicity of Organic Arsenicals
inferred← citeshttps://doi.org/10.1007/s10337-023-04246-3openalex-snapshot
A New Reverse Phase High-Performance Liquid Chromatography (RP-HPLC) Method for Determination of Kinetin Riboside (Plant Hormone) in Dequalinium Chloride Based Self-assembled Vesicles: Development, Validation, and Force Degradation Study
inferred← citeshttps://doi.org/10.1007/s11426-019-9677-7openalex-snapshot
Aggregation-induced emission luminogen for specific identification of malignant tumour in vivo
inferred← citeshttps://doi.org/10.1007/s13596-025-00855-5openalex-snapshot
Oligomeric flavonoids from Cyperus rotundus tubers suppress growth, induce apoptosis, and boost antioxidant defense in multiple cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165808openalex-snapshot
Mitochondria-targeted drug delivery in cancers
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121261openalex-snapshot
Immune-regulating bimetallic metal-organic framework nanoparticles designed for cancer immunotherapy
inferred← citeshttps://doi.org/10.1016/j.drudis.2022.103469openalex-snapshot
Mitochondrial-targeted nanoparticles: Delivery and therapeutic agents in cancer
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.03.036openalex-snapshot
Mitochondria-targeted prooxidant effects of betulinic acid conjugated with delocalized lipophilic cation F16
inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119773openalex-snapshot
Nanotherapeutic approaches to target mitochondria in cancer
inferred← citeshttps://doi.org/10.1016/j.mito.2024.101951openalex-snapshot
Mitochondrial bioenergetics of breast cancer
inferred← citeshttps://doi.org/10.1016/j.molmet.2021.101222openalex-snapshot
Exploring the therapeutic potential of mitochondrial uncouplers in cancer
inferred← citeshttps://doi.org/10.1016/j.nantod.2024.102374openalex-snapshot
A molecularly tailored closed-loop tumor cell energy nanodepleter for cancer starvation therapy
inferred← citeshttps://doi.org/10.1016/j.plrev.2022.09.003openalex-snapshot
The distinguishing electrical properties of cancer cells
inferred← citeshttps://doi.org/10.1016/j.tiv.2020.104907openalex-snapshot
Oligomycin-induced proton uncoupling
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01594openalex-snapshot
Anticancer Activity of Region B Capsaicin Analogs
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5c02076openalex-snapshot
Lipophilic Cations as Mitochondria-Targeting Moieties: Recent Progress and Design Principles for Medicinal Chemistry
inferred← citeshttps://doi.org/10.1038/s41419-020-03251-wopenalex-snapshot
SEMG1/2 augment energy metabolism of tumor cells
inferred← citeshttps://doi.org/10.1038/s41586-019-0993-xopenalex-snapshot
Gboxin is an oxidative phosphorylation inhibitor that targets glioblastoma
inferred← citeshttps://doi.org/10.1038/s41598-017-10949-zopenalex-snapshot
Oscillations of ultra-weak photon emission from cancer and non-cancer cells stressed by culture medium change and TNF-α
inferred← citeshttps://doi.org/10.1038/s41598-020-65450-xopenalex-snapshot
Nanoparticle delivery of a pH-sensitive prodrug of doxorubicin and a mitochondrial targeting VES-H8R8 synergistically kill multi-drug resistant breast cancer cells
inferred← citeshttps://doi.org/10.1038/s41598-021-95278-yopenalex-snapshot
Novel Tl(III) complexes containing pyridine-2,6-dicarboxylate derivatives with selective anticancer activity through inducing mitochondria-mediated apoptosis in A375 cells
inferred← citeshttps://doi.org/10.1038/s43587-026-01122-1openalex-snapshot
Peroxisomes orchestrate metabolic flexibility and longevity via an interorganelle cascade
inferred← citeshttps://doi.org/10.1038/s44324-025-00080-3openalex-snapshot
Mitochondrial uncoupling, energy substrate utilization, and brown adipose tissue as therapeutic targets in cancer
inferred← citeshttps://doi.org/10.1039/d3ma00629hopenalex-snapshot
Circumventing challenges in mitochondrial targeting for cancer treatment: leveraging nanoplatforms for effective solutions
inferred← citeshttps://doi.org/10.1039/d4sc05393aopenalex-snapshot
Photodynamic therapy photosensitizers and photoactivated chemotherapeutics exhibit distinct bioenergetic profiles to impact ATP metabolism
inferred← citeshttps://doi.org/10.1039/d5nr03935eopenalex-snapshot
Emerging nano-delivery systems for targeting mitochondria
inferred← citeshttps://doi.org/10.1093/neuonc/noad099openalex-snapshot
Upstream open reading frame-encoded MP31 disrupts the mitochondrial quality control process and inhibits tumorigenesis in glioblastoma
inferred← citeshttps://doi.org/10.1101/035113openalex-snapshot
Cancer cells have distinct electrical properties that predict a susceptibility to lipophilic anions; a new cancer drug paradigm
inferred← citeshttps://doi.org/10.1101/2021.10.28.466310openalex-snapshot
IF1 Protein Controls Aging Rate
inferred← citeshttps://doi.org/10.1101/2022.09.30.510273openalex-snapshot
Targeting plasma membrane and mitochondrial instability in breast cancer cells and breast epithelial to mesenchymal transition-model cells by adamantyl diaza-crown ether ZG613
inferred← citeshttps://doi.org/10.1101/2025.02.14.638340openalex-snapshot
Peroxisomal Dysfunction Drives Loss of Dynamic Nutrient Responses to Initiate Metabolic Inflexibility During Aging
inferred← citeshttps://doi.org/10.1111/jpi.12536openalex-snapshot
Melatonin‐mediated downregulation of ZNF746 suppresses bladder tumorigenesis mainly through inhibiting the AKT‐MMP‐9 signaling pathway
inferred← citeshttps://doi.org/10.1111/php.13928openalex-snapshot
Mitochondrial targeting improves the selectivity of singlet‐oxygen cleavable prodrugs in NMIBC treatment
inferred← citeshttps://doi.org/10.1111/php.70048openalex-snapshot
Photodynamic priming ( PDP ) targets platinum resistance from chronic perfluoroalkyl substances ( PFAS ) exposure in ovarian cancer cells
inferred← citeshttps://doi.org/10.1134/s1990747823040062openalex-snapshot
Membrane-Active Mitochondria-Targeted Antitumor Agents and Drug Delivery Systems
inferred← citeshttps://doi.org/10.1158/1940-6207.capr-20-0425openalex-snapshot
Mitochondria as a Novel Target for Cancer Chemoprevention: Emergence of Mitochondrial-targeting Agents
inferred← citeshttps://doi.org/10.11606/d.82.2019.tde-27022020-105427openalex-snapshot
Avaliação do efeito citostático e citotóxico na terapia combinada de antineoplásicos em linhagens de câncer de mama (MDA-MB-231), fígado (HepG2) E PRÓSTATA (PC-3 E DU 145)
inferred← citeshttps://doi.org/10.1177/09731296241291625openalex-snapshot
Antiproliferative and Apoptotic Potential of Chicoric Acid, a Major Phytoconstituent of Cichorium intybus , against Colon Cancer Cells: A Possible Inhibition of CDC25 Phosphatases
inferred← citeshttps://doi.org/10.1186/s11671-016-1819-5openalex-snapshot
Fullerene C60 Penetration into Leukemic Cells and Its Photoinduced Cytotoxic Effects
inferred← citeshttps://doi.org/10.1186/s12964-025-02127-wopenalex-snapshot
Targeting mitochondrial proteases CLPP and LONP1 via disruption of mitochondrial redox homeostasis induces proteotoxic stress and suppresses tumor progression
inferred← citeshttps://doi.org/10.1186/s40659-019-0224-9openalex-snapshot
Effects of glutamine deprivation on oxidative stress and cell survival in breast cell lines
inferred← citeshttps://doi.org/10.1530/rem-25-0003openalex-snapshot
Targeting the bioenergetics of a resistant tumor: clinical insights into OXPHOS inhibition for cancer therapy
inferred← citeshttps://doi.org/10.15407/bioorganica2023.01.032openalex-snapshot
New phosphorylated 5-(hydroxyalkylamino)-1,3-oxazoles as potential anticancer agents
inferred← citeshttps://doi.org/10.15407/ubj88.01.044openalex-snapshot
Modulation of cisplatin-induced reactive oxygen species production by fullerene C(60) in normal and transformed lymphoid cells
inferred← citeshttps://doi.org/10.2174/0109298673368188250613112621openalex-snapshot
Recent Advances in the Application of Mitochondria-targeted Fluorescent Probes
inferred← citeshttps://doi.org/10.2174/1389201021666200611113734openalex-snapshot
Dihydroorotate Dehydrogenase Inhibitors Promote Cell Cycle Arrest and Disrupt Mitochondria Bioenergetics in Ramos Cells
inferred← citeshttps://doi.org/10.31083/j.fbl2808180openalex-snapshot
The Role of Mitochondrial Dysfunction in Cytotoxic Effects of Solanum nigrum Water Extract on MCF-7 and MDA-MB-231 Breast Cancer Cells
inferred← citeshttps://doi.org/10.31857/s0233475523040060openalex-snapshot
Membrane-Active Mitochondria-Targeted Antitumor Agents and Drug Delivery Systems
inferred← citeshttps://doi.org/10.32657/10356/165654openalex-snapshot
Augumenting the anticancer properties of l-phenylalanine functionalized nanoscopic porous amino acid mimics (Nano-pPAAMs)
inferred← citeshttps://doi.org/10.3389/fonc.2018.00514openalex-snapshot
Enhanced Cytotoxic Activity of Mitochondrial Mechanical Effectors in Human Lung Carcinoma H520 Cells: Pharmaceutical Implications for Cancer Therapy
inferred← citeshttps://doi.org/10.3390/app9245318openalex-snapshot
Magnetic Fields Trump Oxygen in Controlling the Death of Erythro-Leukemia Cells
inferred← citeshttps://doi.org/10.3390/biom13071112openalex-snapshot
Weak Radiofrequency Field Effects on Chemical Parameters That Characterize Oxidative Stress in Human Fibrosarcoma and Fibroblast Cells
inferred← citeshttps://doi.org/10.3390/biomedicines13071539openalex-snapshot
Betulinic Acid ω-Triphenylphosphonium Alkyl Esters: Antiproliferative Activities and In Silico Pharmacokinetic Profiles
inferred← citeshttps://doi.org/10.3390/biomedicines9101453openalex-snapshot
Feasibility of Photodynamic Therapy for Glioblastoma with the Mitochondria-Targeted Photosensitizer Tetramethylrhodamine Methyl Ester (TMRM)
inferred← citeshttps://doi.org/10.3390/brainsci10020075openalex-snapshot
Using Light for Therapy of Glioblastoma Multiforme (GBM)
inferred← citeshttps://doi.org/10.3390/cancers15092564openalex-snapshot
Methods to Evaluate Changes in Mitochondrial Structure and Function in Cancer
inferred← citeshttps://doi.org/10.3390/clinbioenerg2020009openalex-snapshot
A Narrative Review of the Role of Mitochondria in Cancer: From Metabolic Reprogramming to Therapeutic Targeting
inferred← citeshttps://doi.org/10.3390/ijms22084164openalex-snapshot
A Walk in the Memory, from the First Functional Approach up to Its Regulatory Role of Mitochondrial Bioenergetic Flow in Health and Disease: Focus on the Adenine Nucleotide Translocator
inferred← citeshttps://doi.org/10.3390/md18080417openalex-snapshot
Antimicrobial Peptide TP4 Targets Mitochondrial Adenine Nucleotide Translocator 2
inferred← citeshttps://doi.org/10.3390/nu12030871openalex-snapshot
Queuine Micronutrient Deficiency Promotes Warburg Metabolism and Reversal of the Mitochondrial ATP Synthase in Hela Cells
inferred← citeshttps://doi.org/10.3390/pharmaceutics12070597openalex-snapshot
RETRACTED: The Enhanced Cytotoxic and Pro-Apoptotic Effects of Optimized Simvastatin-Loaded Emulsomes on MCF-7 Breast Cancer Cells
inferred← citeshttps://doi.org/10.3390/pharmaceutics12100956openalex-snapshot
The Encapsulation of Febuxostat into Emulsomes Strongly Enhances the Cytotoxic Potential of the Drug on HCT 116 Colon Cancer Cells
inferred← citeshttps://doi.org/10.3390/pharmaceutics14122657openalex-snapshot
Mitochondrial Dysfunction: Pathophysiology and Mitochondria-Targeted Drug Delivery Approaches
inferred← citeshttps://doi.org/10.5204/thesis.eprints.247163openalex-snapshot
The role of Banf1 in mechanisms of cellular ageing and cancer prognosis
inferred← citeshttps://doi.org/10.64898/2026.03.26.714399openalex-snapshot
Organotin(IV) Dithiocarbamate Compounds Targeting A549 Lung Cancer Cells via Mitochondria-Mediated Apoptosis
inferred← citeshttps://doi.org/10.70675/c8e381a2z8745z4ba5z92c5z245033e340aaopenalex-snapshot
Cationic polymers and N-heterocyclic carbene-metal complexes as anti-cancer stem cell chemotherapeutics
inferred← citeshttps://doi.org/10.7554/elife.99438openalex-snapshot
Mitochondrial protein carboxyl-terminal alanine-threonine tailing promotes human glioblastoma growth by regulating mitochondrial function
inferred← citeshttps://doi.org/10.7554/elife.99438.1openalex-snapshot
The mitochondrial stress-induced protein carboxyl-terminal alanine and threonine tailing (msiCAT-tailing) promotes glioblastoma tumorigenesis by modulating mitochondrial functions
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.