Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
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Cardio-oncology: Concepts and practiceDual Role of ROS as Signal and Stress Agents: Iron Tips the Balance in favor of Toxic EffectsTrial Watch: Immunogenic cell death inducers for anticancer chemotherapyMolecular and Pharmacologic Properties of the Anticancer Quinolone Derivative Vosaroxin: A New Therapeutic Agent for Acute Myeloid LeukemiaSex-specific cardiac cardiolipin remodelling after doxorubicin treatmentHigh-Copy Overexpression Screening Reveals PDR5 as the Main Doxorubicin Resistance Gene in YeastA Biophysical Systems Approach to Identifying the Pathways of Acute and Chronic Doxorubicin Mitochondrial CardiotoxicityBnip3 mediates doxorubicin-induced cardiac myocyte necrosis and mortality through changes in mitochondrial signalingExtracellular control of intracellular drug release for enhanced safety of anti-cancer chemotherapyCancer drug related cardiotoxicity during breast cancer treatment.Visnagin protects against doxorubicin-induced cardiomyopathy through modulation of mitochondrial malate dehydrogenase.21st Century Cardio-Oncology: Identifying Cardiac Safety Signals in the Era of Personalized Medicine.Mice lacking mitochondrial ferritin are more sensitive to doxorubicin-mediated cardiotoxicity.Iron-induced damage in cardiomyopathy: oxidative-dependent and independent mechanisms.SC-III3, a novel scopoletin derivative, induces cytotoxicity in hepatocellular cancer cells through oxidative DNA damage and ataxia telangiectasia-mutated nuclear protein kinase activationCannabidiol Protects against Doxorubicin-Induced Cardiomyopathy by Modulating Mitochondrial Function and Biogenesis.A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients.Novel Anthra[1,2-c][1,2,5]Thiadiazole-6,11-Diones as Promising Anticancer Lead Compounds: Biological Evaluation, Characterization & Molecular Targets DeterminationTargeted Inhibition of Phosphoinositide 3-Kinase/Mammalian Target of Rapamycin Sensitizes Pancreatic Cancer Cells to Doxorubicin without Exacerbating Cardiac ToxicityIncreased Heme Levels in the Heart Lead to Exacerbated Ischemic Injury.Role of autophagy and lysosomal drug sequestration in acquired resistance to doxorubicin in MCF-7 cellsProtective Effects of Dexrazoxane against Doxorubicin-Induced Cardiotoxicity: A Metabolomic Study.Transcriptome-wide co-expression analysis identifies LRRC2 as a novel mediator of mitochondrial and cardiac function.Analysis of redox and apoptotic effects of anthracyclines to delineate a cardioprotective strategy.Drug-induced mitochondrial dysfunction and cardiotoxicity.Potential Roles of Kleinhovia hospita L. Leaf Extract in Reducing Doxorubicin Acute Hepatic, Cardiac and Renal Toxicities in RatsMechanisms of Action and Reduced Cardiotoxicity of Pixantrone; a Topoisomerase II Targeting Agent with Cellular Selectivity for the Topoisomerase IIα Isoform.Reduction in mitochondrial iron alleviates cardiac damage during injuryImpaired mitochondrial function is abrogated by dexrazoxane in doxorubicin-treated childhood acute lymphoblastic leukemia survivors.Heme oxygenase-1 regulates mitochondrial quality control in the heart.Modeling Doxorubicin-Induced Cardiotoxicity in Human Pluripotent Stem Cell Derived-CardiomyocytesDoxorubicin Blocks Cardiomyocyte Autophagic Flux by Inhibiting Lysosome Acidification.Sirt3 protects mitochondrial DNA damage and blocks the development of doxorubicin-induced cardiomyopathy in mice.Therapeutic targeting of autophagy in cardiovascular disease.Photodynamic Therapy Induced Enhancement of Tumor Vasculature Permeability Using an Upconversion Nanoconstruct for Improved Intratumoral Nanoparticle Delivery in Deep TissuesA "Double-Edged" Scaffold: Antitumor Power within the Antibacterial Quinolone.Anthocyanin Attenuates Doxorubicin-Induced Cardiomyotoxicity via Estrogen Receptor-α/β and Stabilizes HSF1 to Inhibit the IGF-IIR Apoptotic Pathway.Doxorubicin Regulates Autophagy Signals via Accumulation of Cytosolic Ca2+ in Human Cardiac Progenitor Cells.Human induced pluripotent stem cell-derived cardiomyocytes recapitulate the predilection of breast cancer patients to doxorubicin-induced cardiotoxicity.Matricellular protein CCN1 mediates doxorubicin-induced cardiomyopathy in mice.
P2860
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P2860
Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
@en
type
label
Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
@en
prefLabel
Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
@en
P2093
P2860
P356
P1476
Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation.
@en
P2093
Arineh Khechaduri
Hossein Ardehali
Marina Bayeva
Mohsen Ghanefar
R Kannan Mutharasan
Rongxue Wu
Sathyamangla V Naga Prasad
Tejaswitha Jairaj Naik
Yoshihiko Ichikawa
P2860
P304
P356
10.1172/JCI72931
P407
P577
2014-01-02T00:00:00Z