Search results for "HEPG2"

showing 10 items of 42 documents

The autoradiographic test for unscheduled DNA synthesis: a sensitive assay for the detection of DNA repair in the HepG2 cell line

2004

International audience; We assessed the DNA-repair capacity of HepG2 cells, which were derived from a human hepatoma, by the unscheduled DNA synthesis assay, using the autoradiography protocol (UDS-AR). We evaluated DNA repair following exposure to direct mutagens (4-nitroquinoline-N-oxide (4-NQO), methyl methanesulfonate (MMS)), to mutagens requiring metabolic activation (benzo[a]pyrene (B[a]P), 2-acetylaminofluorene (2-AAF), N-dimethylnitrosoamine (NDMA)) or to structurally related non-mutagens such as pyrene and 4-acetylaminofluorene (4-AAF). All positive compounds tested induced UDS in HepG2 cells. With 4-NQO and MMS, a concentration-dependent increase in net nuclear grains per cell was…

DNA ReplicationDNA RepairEndpoint DeterminationDNA damageDNA repairHealth Toxicology and Mutagenesis[SDV]Life Sciences [q-bio]Mutagen[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainBiologymedicine.disease_causeHEPG203 medical and health scienceschemistry.chemical_compound0302 clinical medicineTumor Cells CulturedGeneticsmedicineHumansComputingMilieux_MISCELLANEOUS030304 developmental biologyGeneticsAnalysis of Variance0303 health sciencesfungiMolecular biologyMethyl methanesulfonate[SDV] Life Sciences [q-bio]chemistryCell culture030220 oncology & carcinogenesisAutoradiographyRegression AnalysisPyreneGenotoxicityDNAMutagens
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Cytometric analysis for drug-induced steatosis in HepG2 cells

2009

Drugs are capable of inducing hepatic lipid accumulation. When fat accumulates, lipids are primarily stored as triglycerides which results in steatosis and provides substrates for lipid peroxidation. An in vitro multiparametric flow cytometry assay was performed in HepG2 cells by using fluorescent probes to analyze cell viability (propidium iodide, PI), lipid accumulation (BODIPY493/503), mitochondrial membrane potential (tetramethyl rhodamine methyl ester, TMRM) and reactive oxygen species generation (ROS) (2',7'-dihydrochlorofluorescein diacetate, DHCF-DA) as functional markers. All the measurements were restricted to live cells by gating the cells that excluded PI or those that exhibited…

Drug-induced steatosisBiologyToxicologyFluorescenceCell LineFlow cytometryLipid peroxidationchemistry.chemical_compoundIn vivomedicineMultiparametric assayHumansMTT assayPropidium iodideViability assayFlow cytometryHepG2 cellsmedicine.diagnostic_testIn vitro hepatotoxicityGeneral MedicineFlow Cytometrymedicine.diseaseMolecular biologyFatty LiverchemistryCell cultureSteatosisReactive Oxygen Species
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Fluorescent probes on HepG2 cells treated with emergent Fusarium mycotoxins

2012

Fusariumchemistry.chemical_compoundbiologychemistryHepg2 cellsGeneral MedicineToxicologybiology.organism_classificationMycotoxinMicrobiologyToxicology Letters
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POLYMERIC FLUORESCENT NANOPARTICLES BASED ON A POLYASPARTAMIDE FOR IMAGING APPLICATIONS: EVALUATION OF GALACTOSE TARGETING ON HEPG2 CELL INTERNALIZAT…

2014

HEPG2fluorescentpolyaspartamidenanoparticleimagingnanoparticlespolyaspartamide; fluorescent; nanoparticles; HEPG2; imaging
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Biological properties of carotenoids extracted from Halobacterium halobium isolated from a Tunisian solar saltern

2013

Abstract Background Bioactive molecules have received increasing attention due to their nutraceutical attributes and anticancer, antioxidant, antiproliferative and apoptosis-inducing properties. This study aimed to investigate the biological properties of carotenoids extracted from Archaea. Methods Halophilic Archaea strains were isolated from the brine of a local crystallizer pond (TS7) of a solar saltern at Sfax, Tunisia. The most carotenoid-producing strain (M8) was investigated on heptoma cell line (HepG2), and its viability was assessed by the MTT-test. The cells were incubated with different sub-lethal extract rates, with carotenoid concentrations ranging from 0.2 to 1.5 μM. Antioxida…

HalobacteriumTunisiaAntioxidantCell Survivalmedicine.medical_treatmentHepG2 human cancer cellsArchaea Halobacteria Solar saltern Carotenoids HepG2 human cancer cellsBiologymedicine.disease_causeAntioxidantsMicrobiologyHalobacteriachemistry.chemical_compoundNutraceuticalSettore BIO/10 - BiochimicamedicineHumansSeawaterViability assayFood scienceSettore BIO/06 - Anatomia Comparata E CitologiaCell ShapeCarotenoidchemistry.chemical_classificationSolar salternHep G2 CellsGeneral MedicineArchaeaCarotenoidsHalophileOxidative StressComplementary and alternative medicinechemistryCell cultureArachidonic acidOxidative stressResearch Article
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Bu2Sn(N-acetyl-L-cysteinate) antitumor activity on HepG2 cells

2010

HepG2 cellantitumor activityorganotin(IV)
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Comparative cytotoxic study of silica materials functionalised with essential oil components in HepG2 cells

2020

[EN] This work evaluated the cytotoxic effect of different EOCs-functionalised silica particle types. The in vitro toxicity of eugenol and vanillin-immobilised SAS, MCM-41 microparticles and MCM-41 nanoparticles was evaluated on HepG2 cells, and compared to free EOCs and pristine materials. The results revealed that free essential oil components and bare silica had a mild cytotoxic effect on HepG2 cells. However, the comparative study showed that free eugenol and vanillin had a milder cytotoxic effect than the equivalent concentrations of immobilised components on the different silica particles, while differences in cell viability between the bare and functionalised particles relied on the …

HepG2TECNOLOGIA DE ALIMENTOSCell SurvivalCytotoxicityNanoparticleToxicologyMCM-41law.invention03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500404 agricultural biotechnologyMCM-41Microscopy Electron TransmissionlawEugenolOils VolatileCytotoxic T cellHumansCytotoxicityEssential oil030304 developmental biology0303 health sciencesDose-Response Relationship DrugVanillinCationic polymerizationSilica04 agricultural and veterinary sciencesGeneral MedicineHep G2 CellsSilicon Dioxide040401 food scienceEugenolchemistryBenzaldehydesVanillinNanoparticlesFood ScienceNuclear chemistry
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Efectos tóxicos de la zearalenona y sus metabolitos en líneas celulares

2017

La zearalenona (ZEA) y sus metabolitos α-zearalenol (α-ZOL) y β-zearalenol (β-ZOL), son metabolitos secundarios de hongos del genero Fusarium. La ZEA se absorbe y se metaboliza a α-ZOL y β-ZOL. Tanto la ZEA como sus metabolitos producen sus efectos tóxicos por la interacción con los receptores endocrinos aunque no es el único mecanismo por el cual pueden producir toxicidad. Se sabe que, además de disruptores endocrinos la ZEA y sus metabolitos son inmunotóxicos, hepatotóxicos y hematotóxicos causando alteraciones en el sistema reproductivo. La citotoxicidad de la ZEA y sus metabolitos ha sido determinada por distintos tiempos de exposición en diferentes células de mamíferos obteniéndose dif…

HepG2zearalenonaCHO-K1food and beveragescitotoxicidad
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LC-MS untargeted metabolomic analysis of drug-induced hepatotoxicity in HepG2 cells

2015

Hepatotoxicity is the number one cause for agencies not approving and withdrawing drugs for the market. Drug-induced human hepatotoxicity frequently goes undetected in preclinical safety evaluations using animal models. Human-derived in vitro models represent a common alternative to in vivo tests to detect toxic effects during preclinical testing. Most current in vitro toxicity assays rely on the measurement of nonspecific or low sensitive endpoints, which result in poor concordance with human liver toxicity. Therefore, making more accurate predictions of the potential hepatotoxicity of new drugs remains a challenge. Metabolomics, whose aim is to globally assess all the metabolites present …

Human liverClinical BiochemistryHepatotoxinBiologyPharmacologyBioinformaticsBiochemistryAnalytical ChemistryMetabolomicsDrug developmentHepg2 cellsToxicityAnimal testingDrug induced hepatotoxicityELECTROPHORESIS
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Differences in cell proliferation in rodent and human hepatic derived cell lines exposed to ciprofibrate.

2005

International audience; Humans appear to be refractory to some effects of peroxisome proliferators including alterations in cell proliferation, whereas rodents are susceptible. In this study, differences between the human and rat response to peroxisome proliferators were evaluated using rat and human tumour liver cell lines. Rat 7777 cells were more responsive than human HepG2 cells to ciprofibrate as they exhibited a higher decrease in cell number than HepG2, and underwent apoptosis. Results from these studies reveal a surprising response in tumour cell lines as the typical in vivo response of increased cell proliferation and reduced apoptosis was not observed in rat tumour cell lines at c…

MESH : Cell LineCancer ResearchRodentApoptosisMESH : Dose-Response Relationship DrugCell LineClofibric AcidIn vivobiology.animalmedicineMESH : Cell ProliferationAnimals[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyCell ProliferationHypolipidemic AgentsDose-Response Relationship DrugbiologyCell growthMESH : RatsFibric AcidsMESH : LiverMESH : Clofibric AcidRatsCell biologyLiverOncologyApoptosisCell cultureHepg2 cellsCancer researchPeroxisome proliferator-activated receptor alphaCiprofibrateMESH : AnimalsMESH : Apoptosismedicine.drugMESH : Antilipemic Agents
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