Search results for "Assay"

showing 10 items of 2241 documents

Parthenolide sensitizes hepatocellular carcinoma cells to trail by inducing the expression of death receptors through inhibition of STAT3 activation

2011

This article shows that HepG2, Hep3B, and SK-Hep1 cells, three lines of human hepatocellular carcinoma (HCC) cells, are resistant to apoptosis induced by tumor necrosis factor-related apoptosis-inducing ligand (TRAIL). Parthenolide, a sesquiterpene lactone found in European feverfew, has been shown to exert both anti-inflammatory and anti-cancer activities. This article demonstrates that co-treatment with parthenolide and TRAIL-induced apoptosis with synergistic interactions in the three lines of HCC cells. In order to explain these effects we ascertained that parthenolide increased either at protein or mRNA level the total content of death receptors TRAIL-R1 and -R2 as well as their surfac…

STAT3 Transcription FactorCarcinoma HepatocellularPhysiologyClinical BiochemistryCellDown-RegulationTRAILApoptosisPharmacologyParthenolideSTAT3TNF-Related Apoptosis-Inducing Ligandchemistry.chemical_compoundSettore BIO/10 - BiochimicamedicineHumansParthenolidePhosphorylationReceptorSTAT3CaspaseJanus KinasesbiologyLiver NeoplasmsProto-Oncogene Proteins c-mdm2Hep G2 CellsReceptors Death DomainCell BiologyapoptosiEnzyme ActivationGene Expression Regulation Neoplasticmedicine.anatomical_structurechemistryCell cultureApoptosisCaspasesbiology.proteinSTAT proteinDrug Screening Assays AntitumorTumor Suppressor Protein p53SesquiterpenesJournal of Cellular Physiology
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Potassium uptake system Trk2 is crucial for yeast cell viability during anhydrobiosis

2013

Yeasts grow at very different potassium concentrations, adapting their intracellular cation levels to changes in the external environment. Potassium homeostasis is maintained with the help of several transporters mediating the uptake and efflux of potassium with various affinities and mechanisms. In the model yeast Saccharomyces cerevisiae, two uptake systems, Trk1 and Trk2, are responsible for the accumulation of a relatively high intracellular potassium content (200-300 mM) and the efflux of surplus potassium is mediated by the Tok1 channel and active exporters Ena ATPase and Nha1 cation/proton antiporter. Using a series of deletion mutants, we studied the role of individual potassium tra…

Saccharomyces cerevisiae ProteinsATPaseAntiporterPotassiumSaccharomyces cerevisiaechemistry.chemical_elementSaccharomyces cerevisiaeMicrobiologyGeneticsHomeostasisViability assayDesiccationCation Transport ProteinsMolecular BiologySequence DeletionMicrobial ViabilitybiologyBiological Transportbiology.organism_classificationYeastBiochemistrychemistryPotassiumbiology.proteinEffluxIntracellularFEMS Microbiology Letters
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Performance of the auxotrophic Saccharomyces cerevisiae BY4741 as host for the production of IL-1β in aerated fed-batch reactor: role of ACA suppleme…

2009

Abstract Background Saccharomyces cerevisiae BY4741 is an auxotrophic commonly used strain. In this work it has been used as host for the expression and secretion of human interleukin-1β (IL1β), using the cell wall protein Pir4 as fusion partner. To achieve high cell density and, consequently, high product yield, BY4741 [PIR4-IL1β] was cultured in an aerated fed-batch reactor, using a defined mineral medium supplemented with casamino acids as ACA (auxotrophy-complementing amino acid) source. Also the S. cerevisiae mutant BY4741 Δyca1 [PIR4-IL1β], carrying the deletion of the YCA1 gene coding for a caspase-like protein involved in the apoptotic response, was cultured in aerated fed-batch rea…

Saccharomyces cerevisiae ProteinsAuxotrophyInterleukin-1betaMutantBatch reactorSaccharomyces cerevisiaelcsh:QR1-502BioengineeringSaccharomyces cerevisiaeBiologyApplied Microbiology and Biotechnologylcsh:MicrobiologyBioreactorsBioreactorBiomassViability assayAmino AcidsStrain (chemistry)Researchbiology.organism_classificationRecombinant ProteinsGlucoseBiochemistryCaspasesFermentationFermentationBiotechnologyMicrobial Cell Factories
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Cell cycle studies on the mode of action of yeast K28 killer toxin.

1996

The virally encoded K28 killer toxin of Saccharomyces cerevisiae kills sensitive cells by a receptor-mediated process. DNA synthesis is rapidly inhibited, cell viability is lost more slowly and cells eventually arrest, apparently in the S phase of the cell cycle with a medium-sized bud, a single nucleus in the mother cell and a pre-replicated (1n) DNA content. Cytoplasmic microtubules appear normal, and no spindle is detectable. Arrest of a sensitive haploid yeast strain by alpha-factor at START gave complete protection for at least 4 h against a toxin concentration that killed non-arrested cells at the rate of one log each 2.5 h. Cells released from alpha-factor arrest were killed by toxin…

Saccharomyces cerevisiae ProteinsCellSaccharomyces cerevisiaeSaccharomyces cerevisiaeBiologyMicrobiologyMicrotubulesS Phase4-ButyrolactonemedicineViability assayS phaseGeneticsDNA synthesisCell DeathCell CycleDNACell cycleMycotoxinsbiology.organism_classificationFlow CytometryKiller Factors YeastCell biologySpindle poisonmedicine.anatomical_structureCytoplasmFluorescent Antibody Technique Directmedicine.drugMicrobiology (Reading, England)
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Potential Non-Invasive Biomarkers for Early Diagnosis of Oral Squamous Cell Carcinoma

2021

This study aimed to investigate the role of a panel of salivary cytokines as biomarkers for early detection oral squamous cell carcinoma (OSCC), comparing their levels among healthy individuals, patients with oral leukoplakia (OL), and malignant lesions. Cytokine profiling analysis performed in a minimally invasive sample was correlated with clinicopathological variables in our patient cohorts. Unstimulated saliva was obtained from subjects with OSCC at early (n = 33) and advanced (n = 33) disease, OL with homogeneous (n = 33) and proliferative verrucous (n = 33) clinical presentations, and healthy controls (n = 25). Salivary IL-1α, IL-6, IL-8, IP-10, MCP-1, TNF-α, HCC-1, and PF-4 levels we…

Salivamedicine.medical_specialtynon-invasive biomarkerslcsh:MedicineDiseaseGastroenterologyArticleoral leukoplakia03 medical and health sciences0302 clinical medicinesaliva testingSaliva testingInternal medicineMedicineBasal cellmedicine.diagnostic_testbusiness.industrylcsh:RNon invasive biomarkersArea under the curve030206 dentistryGeneral Medicineoral cancer3. Good healthOral leukoplakiastomatognathic diseasestranslational research030220 oncology & carcinogenesisImmunoassaybusinessJournal of Clinical Medicine
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Safety Evaluation of Food contact paper and board using Chemical Tests and in vitro Bioassays-The role of known and unknown substances

2010

International audience; In vitro toxicological tests has have been proposed as an approach to complement the chemical safety assessment of food contact materials, particularly those with a complex or unknown chemical composition such as paper and board. An EU 5th framework program project “BIOSAFEPAPER – Application of bioassays for safety assessment of paper and board for food contact” specially focused on the application of biotests to paper and board. The project included both chemical characterization and toxicological testing of a representative number of paper and board extracts prepared according to the proposed end use (wet, fatty and dry food contact). Among the concerns addressed …

Salmonella typhimuriumFood contact materialsMESH: WoodHealth Toxicology and MutagenesisCytotoxicity[ SDV.TOX ] Life Sciences [q-bio]/Toxicology010501 environmental sciencesmedicine.disease_causeMESH : Gas Chromatography-Mass SpectrometryToxicology01 natural sciencesMESH : Food PackagingMESH : Toxicity Testschemistry.chemical_compoundBioassayMESH: AnimalsMESH : Salmonella typhimuriumChemistryFood PackagingLife Sciences04 agricultural and veterinary sciencesGeneral MedicineWood040401 food scienceMESH : PaperFood packagingMESH : MutagensPackagingFood contact materialsAcrylamideEnvironmental chemistry[SDV.TOX]Life Sciences [q-bio]/ToxicologyToxicityBiological AssayMESH: PaperBioassayPaperMESH: Food PackagingMESH: Cell Line TumorFood Contamination[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainMESH: Biological Assay0404 agricultural biotechnologyCell Line TumorMESH: MutagensmedicineAnimalsHumansMutagenic compoundsMESH: Toxicity Tests0105 earth and related environmental sciencesMESH : WoodChromatographyMESH: Humansbusiness.industryMESH : Cell Line TumorMESH : HumansPublic Health Environmental and Occupational HealthMESH: Salmonella typhimuriumGeneral ChemistryMESH: Food ContaminationFood safetyMESH: Gas Chromatography-Mass SpectrometryMESH : Food ContaminationMESH : AnimalsMESH : Biological AssaybusinessGenotoxicityMutagensFood ScienceFood contaminant
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Evaluation of the SOS/umu-test post-treatment assay for the detection of genotoxic activities of pure compounds and complex environmental mixtures.

2000

This study presents an evaluation of the SOS/umu-test after introducing an additional dilution and incubation in the post-treatment assay. This treatment reduces the influence of coloured test compounds that otherwise affect the colorimetric determination of the beta-galactosidase activity and the bacterial growth measurement during the testing of complex environmental samples. The post-treatment assay significantly increased the beta-galactosidase activity and consequently the enzyme induction ratios at higher doses of model genotoxins 4-nitroquinoline-N-oxide, N-methyl-N'-nitro-N-nitrosoguanidine, 2-aminoanthracene, benzo(a)pyrene with low or no effect on the sensitivity of the test itsel…

Salmonella typhimuriumMethylnitronitrosoguanidineHealth Toxicology and MutagenesisSegmented filamentous bacteriaRecombinant Fusion ProteinsSOS/umu-test; post-treatment assay; S.typhimurium; SOS response; genotoxicity assay; filamentous bacteria; environmental pollutionEnvironmental pollutionDNA-Directed DNA PolymeraseBacterial growthBiologyMicrobiologyAmes testBacterial ProteinsGeneticsBenzo(a)pyreneFood scienceSOS responseSOS Response GeneticsIncubationAnthracenesDose-Response Relationship DrugMutagenicity TestsEscherichia coli Proteinsbiology.organism_classificationbeta-Galactosidase4-Nitroquinoline-1-oxideSOS chromotestEnvironmental PollutantsBacteriaCell DivisionMutagensMutation research
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Increase of sensitivity and validity of the SOS/umu-test after replacement of the beta-galactosidase reporter gene with luciferase.

1998

The SOS/umu-test with Salmonella typhimurium TA1535/pSK1002 as tester strain is a rapid and valuable bacterial assay for screening of umuC-dependent mutagenic potential of chemical compounds and chemicals relevant to environmental pollution. The initial assay was modified by replacing the beta-galactosidase reporter gene with luciferase. Thereby, the sensitivity of the umu-test was increased significantly and the susceptibility to intensively coloured solutions was reduced. The alternative enzyme assay in the modified umu-test (umu-Luc) represents an independent method which allows to confirm the colorimetric results obtained with the original SOS/umu-test system (umu-Gal) by measuring the …

Salmonella typhimuriumSalmonellaHealth Toxicology and MutagenesisBlotting WesternRestriction MappingEnvironmental pollutionmedicine.disease_causeSensitivity and SpecificityGenes ReporterGeneticsmedicineLuciferaseSOS responseLuciferasesSOS Response GeneticsGeneticsReporter genebiologyStrain (chemistry)ChemistryReproducibility of Resultsbeta-GalactosidaseMolecular biologyEnzyme assaybiology.proteinElectrophoresis Polyacrylamide GelGenotoxicityMutation research
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Antibacterial effects of enniatins J1 and J3 on pathogenic and lactic acid bacteria

2011

Abstract Enniatins (ENs) are N -methylated cyclohexadepsipeptides, secondary metabolites produced by various species of the genus Fusarium . They are known to act as antifungal, antiyeast and antibacterial and to possess antiinsecticidal and phytotoxic properties. In this study we evaluated for the first time the antibiotic effect of pure fractions of EN J 1 and J 3 on several pathogenic strains and lactic acid bacteria. The ENs J 1 and J 3 were purified from the fermentation extract of Fusarium solani growth on solid medium of wheat kamut, using the technique of the low pressure liquid chromatography (LPLC) followed by a semipreparative liquid chromatography (LC). The purity and the struct…

SalmonellaChromatographybiologyPathogenic bacteriaMicrobial Sensitivity TestsGeneral MedicineToxicologybiology.organism_classificationmedicine.disease_causeListeria monocytogenesMicrobiologyLactic acidchemistry.chemical_compoundFusariumListeria monocytogeneschemistryLactobacillaceaeDepsipeptidesmedicineBioassayFermentationFusarium solaniBacteriaFood ScienceFood and Chemical Toxicology
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Siderophore production by environmental strains ofSalmonellaspecies

1989

Iron uptake mechanisms were investigated in different species of Salmonella isolated from environmental waters. All strains examined were able to grow in the presence of high concentrations (10 mM) of the iron chelator EDDA. All strains excreted phenolate and hydroxamate siderophores, as assessed by bioassays and chemical tests. Bioassays with different indicator strains showed that all Salmonella strains can cross-feed other Enterobacteria, as well as mutants of Salmonella typhimurium deficient in the Enterobactin system, suggesting that this siderophore may be produced by the environmental Salmonella strains. The siderophore aerobactin may also be produced by one of the strains, according…

SalmonellaSiderophoreBiologybiology.organism_classificationmedicine.disease_causeMicrobiologyEnterobacteriaceaeMicrobiologychemistry.chemical_compoundEnterobactinBiochemistrychemistryGeneticsmedicineAerobactinBioassayBacterial outer membraneMolecular BiologyBacteriaFEMS Microbiology Letters
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