Oxidative Stress-Induced Cellular Senescence: Is Labile Iron the Connecting Link?
暂无分享,去创建一个
[1] A. Goussia,et al. Combined administration of membrane-permeable and impermeable iron-chelating drugs attenuates ischemia/reperfusion-induced hepatic injury. , 2022, Free radical biology & medicine.
[2] K. Vávrová,et al. Examination of diverse iron-chelating agents for the protection of differentiated PC12 cells against oxidative injury induced by 6-hydroxydopamine and dopamine , 2022, Scientific Reports.
[3] K. Engeland. Cell cycle regulation: p53-p21-RB signaling , 2022, Cell Death & Differentiation.
[4] Aditi U. Gurkar,et al. Lipids as Regulators of Cellular Senescence , 2022, Frontiers in Physiology.
[5] F. d’Adda di Fagagna,et al. Telomere dysfunction in ageing and age-related diseases , 2022, Nature Cell Biology.
[6] J. Passos,et al. Cellular senescence: all roads lead to mitochondria , 2022, The FEBS journal.
[7] J. Campisi,et al. The metabolic roots of senescence: mechanisms and opportunities for intervention , 2021, Nature Metabolism.
[8] M. Kharchenko,et al. Outcomes of Deferoxamine Action on H2O2-Induced Growth Inhibition and Senescence Progression of Human Endometrial Stem Cells , 2021, International journal of molecular sciences.
[9] M. Bruchez,et al. Telomeric 8-oxo-guanine drives rapid premature senescence in the absence of telomere shortening , 2021, Nature Structural & Molecular Biology.
[10] E. Gilson,et al. Neutrophils: mediating TelOxidation and senescence , 2021, The EMBO journal.
[11] P. Jat,et al. Mechanisms of Cellular Senescence: Cell Cycle Arrest and Senescence Associated Secretory Phenotype , 2021, Frontiers in Cell and Developmental Biology.
[12] Shane A. Evans,et al. Neutrophils induce paracrine telomere dysfunction and senescence in ROS‐dependent manner , 2021, The EMBO journal.
[13] V. Gorgoulis,et al. Implication of Dietary Iron-Chelating Bioactive Compounds in Molecular Mechanisms of Oxidative Stress-Induced Cell Ageing , 2021, Antioxidants.
[14] Tim Baldensperger,et al. Protein oxidation - Formation mechanisms, detection and relevance as biomarkers in human diseases , 2021, Redox biology.
[15] M. Cavinato,et al. Targeting cellular senescence based on interorganelle communication, multilevel proteostasis, and metabolic control , 2020, The FEBS journal.
[16] K. Pantopoulos,et al. Basics and principles of cellular and systemic iron homeostasis. , 2020, Molecular aspects of medicine.
[17] Dean P. Jones,et al. Reactive oxygen species (ROS) as pleiotropic physiological signalling agents , 2020, Nature Reviews Molecular Cell Biology.
[18] B. Friguet,et al. Proteome Oxidative Modifications and Impairment of Specific Metabolic Pathways During Cellular Senescence and Aging , 2020, Proteomics.
[19] T. Grune. Oxidized protein aggregates: Formation and biological effects. , 2020, Free radical biology & medicine.
[20] N. Mizushima,et al. Lysosome biology in autophagy , 2020, Cell Discovery.
[21] V. Gorgoulis,et al. Implications of Oxidative Stress and Cellular Senescence in Age-Related Thymus Involution , 2020, Oxidative medicine and cellular longevity.
[22] M. Beekman,et al. Senescent human melanocytes drive skin ageing via paracrine telomere dysfunction , 2019, The EMBO journal.
[23] C. Schmitt,et al. Cellular Senescence: Defining a Path Forward , 2019, Cell.
[24] H. Ichijo,et al. Iron homeostasis and iron-regulated ROS in cell death, senescence and human diseases. , 2019, Biochimica et biophysica acta. General subjects.
[25] K. Pantopoulos,et al. Iron homeostasis and oxidative stress: An intimate relationship. , 2019, Biochimica et biophysica acta. Molecular cell research.
[26] E. Fielder,et al. Mitochondrial dysfunction and cell senescence: deciphering a complex relationship , 2019, FEBS letters.
[27] Simon C Watkins,et al. Targeted and Persistent 8-Oxoguanine Base Damage at Telomeres Promotes Telomere Loss and Crisis. , 2019, Molecular cell.
[28] J. Shay,et al. Telomeres and telomerase: three decades of progress , 2019, Nature Reviews Genetics.
[29] S. Cloonan,et al. Mitochondrial Iron in Human Health and Disease. , 2019, Annual review of physiology.
[30] Dean P. Jones,et al. The Exposome: Molecules to Populations. , 2019, Annual review of pharmacology and toxicology.
[31] V. Gorgoulis,et al. In situ evidence of cellular senescence in Thymic Epithelial Cells (TECs) during human thymic involution , 2019, Mechanisms of Ageing and Development.
[32] G. Gestri,et al. Neuropilin-1 Controls Endothelial Homeostasis by Regulating Mitochondrial Function and Iron-Dependent Oxidative Stress , 2018, iScience.
[33] V. Gladyshev,et al. Integrating cellular senescence with the concept of damage accumulation in aging: Relevance for clearance of senescent cells , 2018, Aging cell.
[34] S. Park,et al. Adjustment of the lysosomal-mitochondrial axis for control of cellular senescence , 2018, Ageing Research Reviews.
[35] M. Calero,et al. An Overview of the Role of Lipofuscin in Age-Related Neurodegeneration , 2018, Front. Neurosci..
[36] M. Demaria,et al. Hallmarks of Cellular Senescence. , 2018, Trends in cell biology.
[37] Susan Smith. Telomerase can't handle the stress , 2018, Genes & development.
[38] G. Marverti,et al. Targeting Oxidatively Induced DNA Damage Response in Cancer: Opportunities for Novel Cancer Therapies , 2018, Oxidative medicine and cellular longevity.
[39] Y. Suh,et al. Age- and Tissue-Specific Expression of Senescence Biomarkers in Mice , 2018, Front. Genet..
[40] A. Tzakos,et al. Lipophilic ester and amide derivatives of rosmarinic acid protect cells against H2O2-induced DNA damage and apoptosis: The potential role of intracellular accumulation and labile iron chelation , 2018, Redox biology.
[41] Gopal Jayaraj,et al. Pathways of cellular proteostasis in aging and disease , 2018, The Journal of cell biology.
[42] A. Stier,et al. Does oxidative stress shorten telomeres in vivo? A review , 2017, Biology Letters.
[43] A. Sfera,et al. Ferrosenescence: The iron age of neurodegeneration? , 2017, Mechanisms of Ageing and Development.
[44] B. Stockwell,et al. Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease , 2017, Cell.
[45] Tobias Jung,et al. 4‐Hydroxynonenal (HNE) modified proteins in metabolic diseases , 2017, Free radical biology & medicine.
[46] A. Bush,et al. Iron accumulation in senescent cells is coupled with impaired ferritinophagy and inhibition of ferroptosis , 2017, Redox biology.
[47] Caroline L. Wilson,et al. Cellular senescence drives age-dependent hepatic steatosis , 2017, Nature Communications.
[48] K. Davies,et al. Oxidative DNA damage & repair: An introduction. , 2017, Free radical biology & medicine.
[49] H. Griffiths,et al. Lipid (per) oxidation in mitochondria: an emerging target in the ageing process? , 2017, Biogerontology.
[50] V. Korolchuk,et al. Mitochondria in Cell Senescence: Is Mitophagy the Weakest Link? , 2017, EBioMedicine.
[51] Hanna Salmonowicz,et al. Detecting senescence: a new method for an old pigment , 2017, Aging cell.
[52] S. Rivella,et al. A Red Carpet for Iron Metabolism , 2017, Cell.
[53] Tobias Jung,et al. Mitochondrial contribution to lipofuscin formation , 2017, Redox biology.
[54] Zhe Wang,et al. Autophagy impairment with lysosomal and mitochondrial dysfunction is an important characteristic of oxidative stress-induced senescence , 2017, Autophagy.
[55] J. Lingner,et al. Peroxiredoxin 1 Protects Telomeres from Oxidative Damage and Preserves Telomeric DNA for Extension by Telomerase. , 2016, Cell reports.
[56] Tobias Jung,et al. Happily (n)ever after: Aging in the context of oxidative stress, proteostasis loss and cellular senescence , 2016, Redox biology.
[57] Dimitris Kletsas,et al. Robust, universal biomarker assay to detect senescent cells in biological specimens , 2016, Aging cell.
[58] Michalis D. Mantzaris,et al. Hydroxytyrosol inhibits hydrogen peroxide-induced apoptotic signaling via labile iron chelation , 2016, Redox biology.
[59] S. Myong,et al. Oxidative guanine base damage regulates human telomerase activity , 2016, Nature Structural &Molecular Biology.
[60] A. Thakur,et al. Reduction in mitochondrial iron alleviates cardiac damage during injury , 2016, EMBO molecular medicine.
[61] Ashley I Bush,et al. Iron neurochemistry in Alzheimer's disease and Parkinson's disease: targets for therapeutics , 2016, Journal of neurochemistry.
[62] Laura C. Greaves,et al. Mitochondria are required for pro‐ageing features of the senescent phenotype , 2016, The EMBO journal.
[63] A. Cuervo,et al. Proteostasis and aging , 2015, Nature Network Boston.
[64] D. Baker,et al. Cellular senescence in aging and age-related disease: from mechanisms to therapy , 2015, Nature Medicine.
[65] P. Townsend,et al. The DNA damage response and immune signaling alliance: Is it good or bad? Nature decides when and where. , 2015, Pharmacology & therapeutics.
[66] R. Morimoto,et al. The biology of proteostasis in aging and disease. , 2015, Annual review of biochemistry.
[67] V. Abbate,et al. Iron-sensitive fluorescent probes: monitoring intracellular iron pools. , 2015, Metallomics : integrated biometal science.
[68] M. Conrad,et al. Glutathione peroxidase 4 (Gpx4) and ferroptosis: what's so special about it? , 2015, Molecular & cellular oncology.
[69] H. Sies,et al. Oxidative stress: a concept in redox biology and medicine , 2015, Redox biology.
[70] A. Walch,et al. Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice , 2014, Nature Cell Biology.
[71] R. Brandes,et al. Nox family NADPH oxidases: Molecular mechanisms of activation. , 2014, Free radical biology & medicine.
[72] F. d’Adda di Fagagna,et al. Stable Cellular Senescence Is Associated with Persistent DDR Activation , 2014, PloS one.
[73] Manuel Serrano,et al. Cellular senescence: from physiology to pathology , 2014, Nature Reviews Molecular Cell Biology.
[74] N. Chandel,et al. ROS Function in Redox Signaling and Oxidative Stress , 2014, Current Biology.
[75] P. Gonzalez-Cabo,et al. Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism , 2014, Front. Cell. Neurosci..
[76] Antonio Ayala,et al. Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal , 2014, Oxidative medicine and cellular longevity.
[77] Z. Cabantchik. Labile iron in cells and body fluids: physiology, pathology, and pharmacology , 2014, Front. Pharmacol..
[78] M. Narita,et al. Cellular senescence and its effector programs , 2014, Genes & development.
[79] W. Koppenol,et al. The complex interplay of iron metabolism, reactive oxygen species, and reactive nitrogen species: insights into the potential of various iron therapies to induce oxidative and nitrosative stress. , 2013, Free radical biology & medicine.
[80] J. Sharpe,et al. Senescence Is a Developmental Mechanism that Contributes to Embryonic Growth and Patterning , 2013, Cell.
[81] Manuel Serrano,et al. The Hallmarks of Aging , 2013, Cell.
[82] S. Verhulst,et al. Telomere length behaves as biomarker of somatic redundancy rather than biological age , 2013, Aging cell.
[83] J. Campisi. Aging, cellular senescence, and cancer. , 2013, Annual review of physiology.
[84] T. Grune,et al. Lipofuscin: formation, effects and role of macroautophagy☆ , 2013, Redox biology.
[85] Michalis D. Mantzaris,et al. Lipophilic caffeic acid derivatives protect cells against H2O2-Induced DNA damage by chelating intracellular labile iron. , 2012, Journal of agricultural and food chemistry.
[86] Kerstin Schneeberger,et al. Telomerase gene therapy in adult and old mice delays aging and increases longevity without increasing cancer , 2012, EMBO molecular medicine.
[87] C. Lawless,et al. A senescent cell bystander effect: senescence-induced senescence , 2012, Aging cell.
[88] F. D. D. Fagagna,et al. Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation , 2012, Nature Cell Biology.
[89] Clara Correia-Melo,et al. Telomeres are favoured targets of a persistent DNA damage response in ageing and stress-induced senescence , 2012, Nature Communications.
[90] J. Campisi,et al. Four faces of cellular senescence , 2011, The Journal of cell biology.
[91] V. Lobo,et al. Free radicals, antioxidants and functional foods: Impact on human health , 2010, Pharmacognosy reviews.
[92] O. Soehnlein,et al. Phagocyte partnership during the onset and resolution of inflammation , 2010, Nature Reviews Immunology.
[93] E. Gilson,et al. TRF2/RAP1 and DNA–PK mediate a double protection against joining at telomeric ends , 2010, The EMBO journal.
[94] Tobias Jung,et al. Lipofuscin-bound iron is a major intracellular source of oxidants: role in senescent cells. , 2010, Free radical biology & medicine.
[95] Anil Wipat,et al. Feedback between p21 and reactive oxygen production is necessary for cell senescence , 2010, Molecular systems biology.
[96] E. Arriaga,et al. Mitochondrial turnover and aging of long-lived postmitotic cells: the mitochondrial-lysosomal axis theory of aging. , 2010, Antioxidants & redox signaling.
[97] L. Valenti,et al. Tumorigenesis and Neoplastic Progression Iron-Dependent Regulation of MDM2 Influences p53 Activity and Hepatic Carcinogenesis , 2010 .
[98] Margaret A. Strong,et al. Short telomeres are sufficient to cause the degenerative defects associated with aging. , 2009, American journal of human genetics.
[99] T. de Lange. How Telomeres Solve the End-Protection Problem , 2009, Science.
[100] G. Ferbeyre,et al. Mitochondrial Dysfunction Contributes to Oncogene-Induced Senescence , 2009, Molecular and Cellular Biology.
[101] Michael P. Murphy,et al. How mitochondria produce reactive oxygen species , 2008, The Biochemical journal.
[102] H. Chung,et al. Mitochondrial iron accumulation with age and functional consequences , 2008, Aging cell.
[103] U. Brunk,et al. Lysosomes in iron metabolism, ageing and apoptosis , 2008, Histochemistry and Cell Biology.
[104] K. Pantopoulos,et al. Oxidative Stress and Iron Homeostasis: Mechanistic and Health Aspects , 2008 .
[105] E. Kolettas,et al. Hydrogen peroxide inhibits caspase-dependent apoptosis by inactivating procaspase-9 in an iron-dependent manner. , 2007, Free radical biology & medicine.
[106] Tilman Grune,et al. Lipofuscin: formation, distribution, and metabolic consequences. , 2007, Annals of the New York Academy of Sciences.
[107] M. Blasco,et al. Telomere length, stem cells and aging. , 2007, Nature chemical biology.
[108] U. Brunk,et al. Autophagy, ageing and apoptosis: the role of oxidative stress and lysosomal iron. , 2007, Archives of biochemistry and biophysics.
[109] T. Kirkwood,et al. Mitochondrial Dysfunction Accounts for the Stochastic Heterogeneity in Telomere-Dependent Senescence , 2007, PLoS biology.
[110] W. Zwerschke,et al. Sustained inhibition of oxidative phosphorylation impairs cell proliferation and induces premature senescence in human fibroblasts , 2006, Experimental Gerontology.
[111] F. Petrat,et al. Chelation and determination of labile iron in primary hepatocytes by pyridinone fluorescent probes. , 2006, The Biochemical journal.
[112] U. Brunk,et al. Oxidative stress, accumulation of biological 'garbage', and aging. , 2006, Antioxidants & redox signaling.
[113] K. Riganakos,et al. Protection against nuclear DNA damage offered by flavonoids in cells exposed to hydrogen peroxide: the role of iron chelation. , 2005, Free radical biology & medicine.
[114] T. Lange,et al. Shelterin: the protein complex that shapes and safeguards human telomeres , 2005 .
[115] D. Galaris,et al. DNA protecting and genotoxic effects of olive oil related components in cells exposed to hydrogen peroxide , 2005, Free radical research.
[116] U. Brunk,et al. Role of compartmentalized redox-active iron in hydrogen peroxide-induced DNA damage and apoptosis. , 2005, The Biochemical journal.
[117] Jinshui Fan,et al. Oxidative damage in telomeric DNA disrupts recognition by TRF1 and TRF2 , 2005, Nucleic acids research.
[118] S. Jackson,et al. Functional links between telomeres and proteins of the DNA-damage response. , 2004, Genes & development.
[119] P. Jansen-Dürr,et al. Senescence-associated changes in respiration and oxidative phosphorylation in primary human fibroblasts. , 2004, The Biochemical journal.
[120] B. Ames,et al. Iron Accumulation during Cellular Senescence , 2004, Annals of the New York Academy of Sciences.
[121] S. Oikawa,et al. Mechanism of Telomere Shortening by Oxidative Stress , 2004, Annals of the New York Academy of Sciences.
[122] John M Sedivy,et al. Telomere shortening triggers senescence of human cells through a pathway involving ATM, p53, and p21(CIP1), but not p16(INK4a). , 2004, Molecular cell.
[123] N. Carter,et al. A DNA damage checkpoint response in telomere-initiated senescence , 2003, Nature.
[124] J. Turrens,et al. Mitochondrial formation of reactive oxygen species , 2003, The Journal of physiology.
[125] S. Christoforidis,et al. Endosomal and lysosomal effects of desferrioxamine: protection of HeLa cells from hydrogen peroxide-induced DNA damage and induction of cell-cycle arrest. , 2003, Free radical biology & medicine.
[126] G. Saretzki,et al. MitoQ counteracts telomere shortening and elongates lifespan of fibroblasts under mild oxidative stress , 2003, Aging cell.
[127] T. Tsuzuki,et al. Oxidative nucleotide damage: consequences and prevention , 2002, Oncogene.
[128] Or Kakhlon,et al. The labile iron pool: characterization, measurement, and participation in cellular processes(1). , 2002, Free radical biology & medicine.
[129] C. Chi,et al. Increase in mitochondrial mass in human fibroblasts under oxidative stress and during replicative cell senescence. , 2002, Journal of biomedical science.
[130] U. Brunk,et al. Lipofuscin: mechanisms of age-related accumulation and influence on cell function. , 2002, Free radical biology & medicine.
[131] U. Brunk,et al. The mitochondrial-lysosomal axis theory of aging: accumulation of damaged mitochondria as a result of imperfect autophagocytosis. , 2002, European journal of biochemistry.
[132] B. Frei,et al. Intracellular iron, but not copper, plays a critical role in hydrogen peroxide-induced DNA damage. , 2001, Free radical biology & medicine.
[133] T. Zglinicki,et al. Lipofuscin accumulation in proliferating fibroblasts in vitro: an indicator of oxidative stress , 2001, Experimental Gerontology.
[134] K. Davies. Oxidative Stress, Antioxidant Defenses, and Damage Removal, Repair, and Replacement Systems , 2000, IUBMB life.
[135] S. Oikawa,et al. Site‐specific DNA damage at GGG sequence by oxidative stress may accelerate telomere shortening , 1999, FEBS letters.
[136] M. Blasco,et al. Disease states associated with telomerase deficiency appear earlier in mice with short telomeres , 1999, The EMBO journal.
[137] J. Griffith,et al. Mammalian Telomeres End in a Large Duplex Loop , 1999, Cell.
[138] F. Petrat,et al. Determination of the chelatable iron pool of isolated rat hepatocytes by digital fluorescence microscopy using the fluorescent probe, phen green SK , 1999, Hepatology.
[139] Sandy Chang,et al. Longevity, Stress Response, and Cancer in Aging Telomerase-Deficient Mice , 1999, Cell.
[140] J. Campisi. The biology of replicative senescence. , 1997, European journal of cancer.
[141] G. Saretzki,et al. Mild hyperoxia shortens telomeres and inhibits proliferation of fibroblasts: a model for senescence? , 1995, Experimental cell research.
[142] P. Kruk,et al. DNA damage and repair in telomeres: relation to aging. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[143] D. McLachlan,et al. Intramuscular desferrioxamine in patients with Alzheimer's disease , 1991, The Lancet.
[144] C. Harley,et al. Telomeres shorten during ageing of human fibroblasts , 1990, Nature.
[145] R. S. Sohal,et al. Effect of ferric iron and desferrioxamine on lipofuscin accumulation in cultured rat heart myocytes , 1988, Mechanisms of Ageing and Development.
[146] S. Linn,et al. Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro. , 1988, Science.
[147] A M Olovnikov,et al. A theory of marginotomy. The incomplete copying of template margin in enzymic synthesis of polynucleotides and biological significance of the phenomenon. , 1973, Journal of theoretical biology.
[148] J. D. Watson. Origin of Concatemeric T7DNA , 1972 .
[149] L. Hayflick,et al. The serial cultivation of human diploid cell strains. , 1961, Experimental cell research.
[150] J. Lingner,et al. Impact of oxidative stress on telomere biology. , 2018, Differentiation; research in biological diversity.
[151] I. Wittig,et al. Generator-specific targets of mitochondrial reactive oxygen species. , 2015, Free radical biology & medicine.
[152] L. Defebvre,et al. Targeting Chelatable Iron as a Therapeutic Modality in Parkinson ’ s Disease , 2016 .
[153] D. Galaris,et al. Protective Effects of Olive Oil Components Against Hydrogen Peroxide-Induced DNA Damage: The Potential Role of Iron Chelation , 2010 .
[154] T. de Lange,et al. Shelterin: the protein complex that shapes and safeguards human telomeres. , 2005, Genes & development.
[155] T. von Zglinicki. Oxidative stress shortens telomeres. , 2002, Trends in biochemical sciences.
[156] T. Zglinicki,et al. Accumulation of single-strand breaks is the major cause of telomere shortening in human fibroblasts. , 2000, Free radical biology & medicine.
[157] T. Zglinicki,et al. Lipofuscin accumulation and ageing of fibroblasts. , 1995, Gerontology.
[158] M Chevion,et al. A site-specific mechanism for free radical induced biological damage: the essential role of redox-active transition metals. , 1988, Free radical biology & medicine.