Search results for "Agens"

showing 10 items of 172 documents

Sulfotransferase-mediated chlorination of 1-hydroxymethylpyrene to a mutagen capable of penetrating indicator cells.

1990

Methylated polycyclic aromatic hydrocarbons are common in the human environment. Many of them are stronger carcinogens than their purely aromatic congeners. They may be metabolized to benzylic alcohols. We report here on biochemical and toxicological characteristics of 1-hydroxymethylpyrene (HMP), a typical representative of this class of compounds. Rat liver cytosol, fortified with 3'-phosphoadenosine-5'-phosphosulfate, converted HMP into its sulfate ester (HMPS), HMPS bound covalently to isolated DNA. In physiological buffer at 37 degrees C, HMPS had a half-life of 2 min, the major decomposition product being HMP. Thus, cyclic activation is possible. When Cl- anions were present at physio…

MaleSulfotransferaseHealth Toxicology and MutagenesisMutagenIn Vitro Techniquesmedicine.disease_causeAdductchemistry.chemical_compoundBiotransformationChloridesmedicineAnimalsCarcinogenBiotransformationchemistry.chemical_classificationPyrenesMutagenicity TestsCell MembranePublic Health Environmental and Occupational HealthRats Inbred StrainsRatsEnzymechemistryBiochemistryLiverPyreneSulfotransferasesDNAResearch ArticleMutagensEnvironmental Health Perspectives
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Organometallic complexes with biological molecules. XVIII. Alkyltin(IV) cephalexinate complexes: synthesis, solid state and solution phase investigat…

2004

Abstract Dialkyltin(IV) and trialkyltin(IV) complexes of the deacetoxycephalo-sporin-antibiotic cephalexin [7-( d -2-amino-2-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid] (Hceph) have been synthesized and investigated both in solid and solution phase. Analytical and thermogravimetric data supported the general formula Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O (Alk=Me, n -Bu), while structural information has been gained by FT-IR, 119 Sn Mossbauer and 1 H, 13 C, 119 Sn NMR data. In particular, IR results suggested polymeric structures both for Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O. Moreover, cephalexin appears to behave as monoanionic tridentate ligand coordinating th…

MaleThermogravimetric analysisDenticitySpectrophotometry InfraredStereochemistryMolecular Conformationchemistry.chemical_elementorganotin(IV)proton nuclear magnetic resonanceBiochemistryMedicinal chemistryChromosomesMossbauerInorganic ChemistrySpectroscopy Mossbauerchemistry.chemical_compoundantibiotic; cephalexin; organotin(IV); Mossbauer; cytotoxicitySpermatocytescomplex formationantibioticMössbauer spectroscopyOrganotin CompoundsAnimaliaAnimalsMoietyBrachidontes pharaoniCarboxylateNuclear Magnetic Resonance BiomolecularCephalexinMolecular StructureChemistryarticlesolid stateNuclear magnetic resonance spectroscopycarbon nuclear magnetic resonanceBivalviaAnti-Bacterial AgentsspermatocyteSettore CHIM/03 - Chimica Generale E InorganicaMolluscaThermogravimetryMössbauercytotoxicitycefalexinorganometallic compoundChromosome breakagedrug synthesiTinMutagensJournal of Inorganic Biochemistry
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Effects of β-Carotene, Retinal, Riboflavin, α-Tocopherol and Vitamins C and K1 on Sister-chromatid Exchanges Induced by 3-Amino-1-methyl-5H-pyrido[4,…

1998

The vitamins and related compounds cited in the title were investigated for their abilities to modulate sister-chromatid exchanges (SCEs) induced by Trp-P-2 or cyclophosphamide (CP) in human peripheral lymphocyte cultures in the presence of an exogenous metabolizing system from rat liver. When inducer and test substances were given simultaneously, beta-carotene, retinal and alpha-tocopherol caused a dose-dependent decrease of SCE frequencies induced by Trp-P-2 and CP. Vitamin K1, however, brought about an identical effect with Trp-P-2 only, while with CP an initial decrease of SCEs was followed by a statistically significant re-increase at higher concentrations. Vitamin C was ineffective ag…

MaleVitaminmedicine.medical_specialtyRiboflavinT-Lymphocytesmedicine.medical_treatmentRiboflavinAscorbic AcidToxicologyAntioxidantsRats Sprague-Dawley03 medical and health scienceschemistry.chemical_compound0302 clinical medicineInternal medicinemedicineAnimalsHumansVitamin ETocopherolCyclophosphamideCells Cultured030304 developmental biology0303 health sciencesVitamin CChemistryVitamin ERetinolVitamin K 1VitaminsGeneral Medicinebeta CaroteneAscorbic acidRats3. Good healthEndocrinologyBiochemistry030220 oncology & carcinogenesisRetinaldehydealpha-TocopherolSister Chromatid ExchangeCarbolinesMutagensFood ScienceFood and Chemical Toxicology
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Rac1 GTPase, a multifunctional player in the regulation of genotoxic stress response

2013

The Ras-related C3 botulinum toxin substrate 1 (Rac1) belongs to the Ras-homologous (Rho) family of small GTPases, which transduce signals from the outside to the inside of a cell. Rac1 becomes activated upon ligand binding of a variety of receptors, including receptor tyrosine kinases and heterotrimeric G-protein-coupled receptors. After GTP loading by guanine exchange factors (GEFs), GTP-bound Rac1 engages numerous effector proteins, thereby eventually regulating cell motility and adhesion, cell cycle progression through G1, mitosis and meiosis, as well as cell death and metastasis.1 Besides, Rac1 adjusts cellular responses to genotoxic agents, such as UV light and alkylating agents, by r…

Malerac1 GTP-Binding Proteintopoisomerase IIAgingRHOADNA repairDNA damagep38 mitogen-activated protein kinasesApoptosisRAC1Editorials: Cell Cycle FeaturesDNA damage responseReceptor tyrosine kinasechemical carcinogenesisHistonesMiceTransforming Growth Factor betaRho GTPasesAnimalsMolecular BiologyTranscription factoranthracyclinesMice KnockoutbiologyKinaseNeuropeptidesConnective Tissue Growth FactorHMG-CoA reductase inhibitors (statins)Cell BiologyFibrosisgenotoxic stressActinsrac GTP-Binding ProteinsCell biologyOxidative Stressnormal tissue damageGene Expression RegulationLiverBiochemistryDoxorubicinGamma Raysbiology.proteinFemaleDNA DamageMutagensSignal TransductionDevelopmental BiologyCell Cycle
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A mechanistic model on the role of “radially-running” collagen fibers on dissection properties of human ascending thoracic aorta.

2014

Aortic dissection (AoD) is a common condition that often leads to life-threatening cardiovascular emergency. From a biomechanics viewpoint, AoD involves failure of load-bearing microstructural components of the aortic wall, mainly elastin and collagen fibers. Delamination strength of the aortic wall depends on the load-bearing capacity and local micro-architecture of these fibers, which may vary with age, disease and aortic location. Therefore, quantifying the role of fiber micro-architecture on the delamination strength of the aortic wall may lead to improved understanding of AoD. We present an experimentally-driven modeling paradigm towards this goal. Specifically, we utilize collagen fib…

Materials sciencePeel forceFibrillar Collagens0206 medical engineeringBiomedical EngineeringBiophysicsAorta Thoracic02 engineering and technologyDissection (medical)030204 cardiovascular system & hematologyFiber bridge failure modelArticleWeight-Bearing03 medical and health sciences0302 clinical medicinemedicine.arteryCollagen fibermedicineAnimalsHumansThoracic aortaOrthopedics and Sports MedicineFiberAortaAortic dissectionAortaAortic Aneurysm ThoracicbiologyDissectionRehabilitationDelaminationModels CardiovascularBiomechanicsAnatomymedicine.disease020601 biomedical engineeringBiomechanical PhenomenaElastinExtracellular MatrixAortic Dissectionbiology.proteinFemaleElastinBiomedical engineering
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Xrcc2 deficiency sensitizes cells to apoptosis by MNNG and the alkylating anticancer drugs temozolomide, fotemustine and mafosfamide

2006

DNA double-strand breaks (DSBs) are potent killing lesions, and inefficient repair of DSBs does not only lead to cell death but also to genomic instability and tumorigenesis. DSBs are repaired by non-homologous end-joining and homologous recombination (HR). A key player in HR is Xrcc2, a Rad51-like protein. Cells deficient in Xrcc2 are hypersensitive to X-rays and mitomycin C and display increased chromosomal aberration frequencies. In order to elucidate the role of Xrcc2 in resistance to anticancer drugs, we compared Xrcc2 knockout (Xrcc2-/-) mouse embryonic fibroblasts with the corresponding isogenic wild-type and Xrcc2 complemented knockout cells. We show that Xrcc2-/- cells are hypersen…

MethylnitronitrosoguanidineCancer ResearchProgrammed cell deathDNA repairDNA damageMitomycinApoptosisBiologyNitrosourea Compoundschemistry.chemical_compoundOrganophosphorus CompoundsMafosfamideTemozolomidemedicineHumansCytotoxic T cellAntineoplastic Agents AlkylatingCyclophosphamideCisplatinMolecular biologyDNA-Binding ProteinsDacarbazineOncologychemistryApoptosisFotemustineCisplatinMutagensmedicine.drugCancer Letters
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Photoinduced intersystem crossing in DNA oxidative lesions and epigenetic intermediates

2020

[EN] The propensity of 5-formyluracil and 5-formylcytosine, i.e. oxidative lesions and epigenetic intermediates, in acting as intrinsic DNA photosensitizers is unraveled by using a combination of molecular modeling, simulation and spectroscopy. Exploration of potential energy surfaces and non-adiabatic dynamics confirm a higher intersystem crossing rate for 5-formyluracil, whereas the kinetic models evidence different equilibria in the excited states for both compounds.

Models MolecularMolecular modelLightOxidative phosphorylation010402 general chemistry01 natural sciencesCatalysisEpigenesis Geneticchemistry.chemical_compoundCytosineQUIMICA ORGANICAMaterials Chemistry[CHIM]Chemical SciencesHumansComputer SimulationEpigeneticsSpectroscopyUracilComputingMilieux_MISCELLANEOUS010405 organic chemistryChemistryMetals and AlloysGeneral ChemistryDNAPotential energy0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsKineticsIntersystem crossingExcited stateCeramics and CompositesBiophysicsOxidation-ReductionDNAMutagens
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Temnothorax pilagens sp. n. – a new slave-making species of the tribe Formicoxenini from North America (Hymenoptera, Formicidae)

2014

A new species of the ant genus Temnothorax Forel, 1890 – Temnothorax pilagens sp. n. is described from eastern North America. T. pilagens sp. n. is an obligate slave-making ant with two known hosts: T. longispinosus (Roger, 1863) and T. ambiguus (Emery, 1895). A differential diagnosis against Temnothorax duloticus (Wesson, 1937), the other dulotic congener from the Nearctic, is presented and a biological characteristics of the new species is given.

MorphometricsNearctic regionmorphometricsbiologyTemnothoraxObligateEcologyved/biologyved/biology.organism_classification_rank.speciesslave-raiding behaviorTemnothorax pilagensZoologyHymenopteraTribe (biology)biology.organism_classificationArticledulosisTemnothoraxGenuslcsh:ZoologyNearctic ecozoneAnimal Science and Zoologylcsh:QL1-991Ecology Evolution Behavior and SystematicsZooKeys
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Changes in protein domains outside the catalytic site of the bacteriophage Qβ replicase reduce the mutagenic effect of 5-azacytidine.

2014

ABSTRACT The high genetic heterogeneity and great adaptability of RNA viruses are ultimately caused by the low replication fidelity of their polymerases. However, single amino acid substitutions that modify replication fidelity can evolve in response to mutagenic treatments with nucleoside analogues. Here, we investigated how two independent mutants of the bacteriophage Qβ replicase (Thr210Ala and Tyr410His) reduce sensitivity to the nucleoside analogue 5-azacytidine (AZC). Despite being located outside the catalytic site, both mutants reduced the mutation frequency in the presence of the drug. However, they did not modify the type of AZC-induced substitutions, which was mediated mainly by …

Mutation rateImmunologyMutantRNA-dependent RNA polymeraseBiologyVirus ReplicationMicrobiologyViral ProteinsVirologyCatalytic DomainmedicineGeneticsAllolevivirusNucleoside analogueQ beta Replicasebiology.organism_classification3. Good healthProtein Structure TertiaryViral replicationBiochemistryAmino Acid SubstitutionGenetic Diversity and EvolutionInsect ScienceAzacitidineQ beta ReplicaseBacteriophage QβNucleosidemedicine.drugMutagensJournal of virology
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Modulation of mutagenicity by phosphorylation of mutagen-metabolizing enzymes.

2004

In this Minireview, we discuss our findings on phosphorylation of cytochromes P450 (CYP) and influence of this modification on metabolic toxification and/or detoxification of a variety of mutagens. We show that phosphorylation drastically interferes with the mutagenicity of several classes of compounds which are of high human relevance (cytostatic drugs of the cyclophosphamide type, aromatic amines/amides, and nitrosamines). We illustrate this by describing the consequences of the stimulation of protein kinase A (with the example of CYP2B1 and CYP2E1), stimulation of protein kinase C, and inhibition of protein phosphatases PP1 and PP2A (with the example of CYP1A1 and CYP1A2). We discuss a p…

NitrosaminesPhosphataseBiophysicsMutagenmacromolecular substancesmedicine.disease_causeenvironment and public healthBiochemistryDimethylnitrosamineCytochrome P-450 Enzyme SystemmedicineSerineAnimalsHumansProtein phosphorylationPhosphorylationProtein kinase AMolecular BiologyProtein kinase CChemistryProtein phosphatase 2CYP2E1EnzymesRatsenzymes and coenzymes (carbohydrates)BiochemistryPhosphorylationMutagensArchives of biochemistry and biophysics
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