Search results for "Genetic transfer"

showing 10 items of 29 documents

Successful adenovirus-mediated wild-type p53 gene transfer in patients with bladder cancer by intravesical vector instillation.

2002

PURPOSE: To study safety, feasibility, and biologic activity of adenovirus-mediated p53 gene transfer in patients with bladder cancer. PATIENTS AND METHODS: Twelve patients with histologically confirmed bladder cancer scheduled for cystectomy were treated on day 1 with a single intratumoral injection of SCH 58500 (rAd/p53) at cystoscopy at one dose level (7.5 × 1011 particles) or a single intravesical instillation of SCH 58500 with a transduction-enhancing agent (Big CHAP) at three dose levels (7.5 × 1011 to 7.5 × 1013 particles). Cystectomies were performed in 11 patients on day 3, and transgene expression, vector distribution, and biologic markers of transgene activity were assessed by m…

AdultCancer ResearchPathologymedicine.medical_specialtymedicine.medical_treatmentGenetic enhancementGenetic VectorsUrologyCystectomyAdenoviridaeCystectomymedicineHumansNeoplasm InvasivenessAgedDNA PrimersBiologic markerAged 80 and overUrinary bladderBladder cancermedicine.diagnostic_testDose-Response Relationship Drugbusiness.industryReverse Transcriptase Polymerase Chain ReactionGenetic transferGene Transfer TechniquesCystoscopyGenetic TherapyMiddle Agedmedicine.diseaseGenes p53medicine.anatomical_structureAdministration IntravesicalOncologyUrinary Bladder NeoplasmsImmunohistochemistrybusinessJournal of clinical oncology : official journal of the American Society of Clinical Oncology
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Polyhydroxyethylaspartamide-spermine copolymers: Efficient vectors for gene delivery

2008

Abstract Aim of this paper was that to prepare biocompatible, polyaspartamide based copolymers containing spermine or spermine/hydrophobic side chains able to condense nucleic acids and to transfect mammalian cells. Copolymers were prepared starting from α,β-poly-(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) and exploiting the reactive hydroxyl groups in the polymeric side chains by subsequent activation reactions to obtain PHEA-Spermine (PHEA-Spm) and PHEA-Spermine-Butyramide (PHEA-Spm-C4). Molecular, physico-chemical and biological characterization of copolymers and interpolyelectrolyte complexes with plasmid DNA was performed. Experimental results evidenced that these copolymers are able…

Biocompatibilitygene delivery polyaspartamideCell SurvivalStereochemistryPharmaceutical ScienceSpermineGene deliveryBiologyTransfectionpolycationDNA Adductschemistry.chemical_compoundCell Line TumorCopolymerHumansLuciferasesCells CulturedErythrocyte MembraneGenetic transferinterpolyelectrolyte complexesGene Transfer TechniquesDNATransfectionCombinatorial chemistrychemistryNucleic acidSperminePeptidesDNAJournal of Controlled Release
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Induction of immunogenicity of a human renal-cell carcinoma cell line byTAP1-gene transfer

1999

Reduced expression of the major-histocompatibility-complex(MHC)-class-I antigens has been demonstrated in renal-cell carcinoma (RCC), and appeared to be associated with deficiencies in the expression and function of different components of the MHC-class-I-antigen-processing pathway and poor recognition by cytotoxic T-lymphocytes (CTL). In order to investigate the role of peptide transporters for the immunogenic phenotype of RCC, tumor cells were stably transfected with the human TAP1A gene. While the TAP1 transfectants showed heterogeneous TAP1-transgene expression pattern of mRNA and protein, high TAP1 expression and a TAP-controlled increase in MHC-class-I surface expression could be achi…

Cancer ResearchGenetic transferTransfectionBiologyurologic and male genital diseasesMajor histocompatibility complexImmune toleranceImmune systemOncologyAntigenCell cultureImmunologyCancer researchbiology.proteinCytotoxic T cellInternational Journal of Cancer
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Novel cationic solid-lipid nanoparticles as non-viral vectors for gene delivery.

2007

In this paper, the suitability of novel cationic solid-lipid nanoparticles (SLN) as a nonviral transfection agent for gene delivery was investigated. SLN were produced by using the microemulsion method and Compritol ATO 888 as matrix lipid, dimethyldioctadecylammonium bromide as charge carrier and Pluronic F68 as surfactant. Obtained nanoparticles were approximately 120 nm in size and positively charged, with a zeta potential value equal to +45 mV in twice-distilled water. Cationic SLN were able to form stable complexes with DNA and to protect DNA against DNase I digestion. The SLN-DNA complexes were characterized by mean diameter and zeta potential measurements. In vitro studies on human l…

Cell SurvivalPharmaceutical ScienceGene deliveryBiologyTransfectionGlyceridesPulmonary surfactantCationsCell Line TumorSolid lipid nanoparticleZeta potentialHumansParticle Sizeeducationeducation.field_of_studyDrug CarriersGenetic transferCationic polymerizationGene Transfer TechniquesTransfectionDNAlipid nanoparticles gene deliverybeta-GalactosidaseBiochemistryBiophysicsNanoparticlesDimethyldioctadecylammonium bromideJournal of drug targeting
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Culture medium induced vimentin reorganization associates with enhanced baculovirus-mediated gene delivery.

2009

Baculoviruses can express transgenes under mammalian promoters in a wide range of vertebrate cells. However, the success of transgene expression is dependent on both the appropriate cell type and culture conditions. We studied the mechanism behind the substantial effect of the cell culture medium on efficiency of the baculovirus transduction in different cell lines. We tested six cell culture mediums; the highest transduction efficiency was detected in the presence of RPMI 1640 medium. Vimentin, a major component of type III intermediate filaments, was reorganized in the optimized medium, which associated with enhanced nuclear entry of baculoviruses. Accordingly, the phosphorylation pattern…

Cell typebiologyvirusesGenetic transferCell Culture TechniquesBioengineeringVimentinGeneral MedicineGene deliveryApplied Microbiology and BiotechnologyMolecular biologyCulture MediaTransduction (genetics)Cell cultureTransduction GeneticDNA Viralbiology.proteinAnimalsHumansVimentinIntermediate filamentCytoskeletonBaculoviridaeCells CulturedBiotechnologyJournal of biotechnology
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Conservation of type III secretion system genes inBradyrhizobiumisolated from soybean

2006

International audience; The distribution of rhcRST genes encoding the type III secretion system (T3SS) in a collection of Bradyrhizobium strains was characterized by PCR and Southern blot hybridization. The polymorphism of the corresponding sequences amplified by PCR was characterized by RFLP and sequencing together with those available in the databank. Genomic group I is characterized by the presence of Bradyrhizobium elkanii strains and group II by the presence of B. japonicum and B. liaoningense strains. Highly conserved T3SS-like genes were detected by PCR in all Bradyrhizobium strains isolated from soybean belonging to genomic group II, and in none of the strains belonging to genomic g…

DNA BacterialGenotyperhc genessinorhizobiumhrc genesMicrobiologyBradyrhizobiummicroorganisme du sollaw.invention03 medical and health scienceslawGeneticsRELATION PLANTE-MICROORGANISMESymbiosisMolecular BiologyGenePhylogenyBradyrhizobium elkaniiPolymerase chain reaction030304 developmental biologySouthern blotGenetics0303 health sciencesBase Sequencebradyrhizobiumbiologymesorhizobium030306 microbiologyGenetic transferbiochemical phenomena metabolism and nutritionRibosomal RNAbiology.organism_classificationtype III secretion system-T3SSRNA BacterialPhenotype[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyGenes BacterialRNA RibosomalbacteriaSoybeansRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthFEMS Microbiology Letters
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Distribution and diversity of type III secretion system-like genes in saprophytic and phytopathogenic fluorescent pseudomonads

2004

Type three secretion systems (TTSSs) are protein translocation mechanisms associated with bacterial pathogenicity in host plants, and hypersensitive reactions in non-host plants. Distribution and diversity of TTSS-like genes within a collection of saprophytic and phytopathogenic fluorescent pseudomonads were characterized. This collection included 16 strains belonging to 13 pathogenic species, and 87 strains belonging to five saprophytic species isolated from plant rhizosphere and soil. Presence of conserved hypersensitive reaction/pathogenicity (hrp) genes (hrc RST) was assessed both by PCR using primers designed to amplify the corresponding sequence and by dot-blot hybridization using a P…

DNA BacterialMolecular Sequence DataBiologyPlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyMicrobiologyFluorescenceMicrobiologyType three secretion systemlaw.inventionPSEUDOMOMAS FLUORESCENS03 medical and health sciencesBacterial ProteinslawPseudomonasRNA Ribosomal 16SGenotypeGene[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologySoil MicrobiologyPolymerase chain reactionComputingMilieux_MISCELLANEOUSPlant Diseases030304 developmental biology2. Zero hungerGenetics0303 health sciencesEcology030306 microbiologyGenetic transferGenetic VariationSequence Analysis DNAPlants16S ribosomal RNAbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyPOUVOIR PATHOGENERestriction fragment length polymorphismPolymorphism Restriction Fragment LengthBacteria
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R plasmids in environmental Vibrio cholerae non-O1 strains.

1988

The occurrence of drug resistance and its plasmid-mediated transferability was investigated in 140 environmental strains of Vibrio cholerae non-O1 and 6 strains of Vibrio cholerae, both O1 and non-O1, of clinical origin. Of the 146 strains tested, 93% were resistant to at least one drug and 74% were resistant to two or more antibiotics. The O1 strains were susceptible to all antibiotics used. A total of 26 of 28 selected resistant wild strains carried R plasmids that were transferable by intraspecific and intergeneric matings. The most common transmissible R factor determined resistance to ampicillin, amoxicillin, and sulfanilamide (30%), followed by resistance to ampicillin and amoxicillin…

DNA BacterialR FactorsFresh WaterDrug resistancemedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyPlasmidVibrio cholerae non-O1VibrionaceaeAmpicillinmedicineSeawaterVibrio choleraeElectrophoresis Agar GelEcologybiologyVirulenceGenetic transferDrug Resistance MicrobialSulfanilamidebiology.organism_classificationAnti-Bacterial AgentsVibrio choleraeConjugation GeneticWater MicrobiologyFood ScienceBiotechnologymedicine.drugResearch Article
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Novel Biocompatible Cationic Copolymers Based on Polyaspartylhydrazide Being Potent as Gene Vector on Tumor Cells

2007

Introduction. The reaction between !,"-poly(aspartylhydrazide) (PAHy), a water soluble synthetic polymer and 3-(carboxypropyl)trimethyl-ammonium chloride (CPTACl) produced copolymers bearing permanent positive charges (PAHy–CPTA) with molecular weight of 10 kDa and PAHy–CPTA copolymers differing in positive charge amount (18–58%) were chosen for biological investigations. Materials and methods. Biophysical properties of DNA/PAHy–CPTA polyplexes were evaluated in terms of DNA condensation, zeta potential and size distribution. Cytotoxicity studies on Neuro2A murine neuroblastoma cells evidenced absence of toxicity of these copolymers up to 300 2g/ml unlike linear polyethylenimine (LPEI) that…

Erythrocyte AggregationBiocompatibilityCell SurvivalPolymersPharmaceutical ScienceBiocompatible MaterialsBiologyTransfectionDNA condensationMiceNeuroblastomachemistry.chemical_compoundIn vivoCationsCell Line TumorZeta potentialAnimalsPolyethyleneiminePharmacology (medical)Particle SizeCytotoxicityPharmacologyPolyethylenimineCytotoxicity liver toxicity nonviral gene delivery transfectionDose-Response Relationship DrugLiver DiseasesBody WeightOrganic ChemistryGenetic transferDNATransfectionMolecular WeightLiverchemistryBiochemistryNucleic Acid ConformationMolecular MedicineFemaleChemical and Drug Induced Liver InjuryPeptidesBiotechnologyPharmaceutical Research
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Horizontal gene transfer of atrazine-degrading genes (atz) from Agrobacterium tumefaciens St96-4 pADP1::Tn5 to bacteria of maize-cultivated soil

2005

International audience; The plasmid pADP1::Tn5 derived from pADP1[Atr(+)] carrying a TnS transposon conferring kanamycin and streptomycin resistances was constructed and introduced in Agrobacterium tumefaciens St96-4. This genetically modified strain was inoculated (similar to 108 cfu g(-1)) in potted soils planted with maize and treated or not with atrazine (1.5 mg kg(-1)). Bulk and maize rhizosphere soils were sampled 39 days after planting to look for soil indigenous bacteria that had acquired pADP1::Tn5. Four transconjugants were isolated from four different soil samples. The estimated transfer frequency of pADP1::Tn5 was 10(-4) per donor. Maize rhizosphere and atrazine treatment had no…

Gene Transfer HorizontalATRAZINE[SDV]Life Sciences [q-bio]BIODEGRADATIONZea mays03 medical and health scienceschemistry.chemical_compoundBotanymedicineATZ GENESAtrazinePhylogenySoil Microbiology030304 developmental biology2. Zero hunger0303 health sciencesRhizospherebiologyOrganisms Genetically Modified030306 microbiologyHerbicidesGenetic transferHORIZONTAL GENE TRANSFERKanamycinGeneral MedicineGene rearrangementAgrobacterium tumefaciensVariovoraxbiochemical phenomena metabolism and nutritionbiology.organism_classificationBiodegradation EnvironmentalchemistryAgrobacterium tumefaciensInsect ScienceConjugation Genetic[SDE]Environmental SciencesbacteriaAgronomy and Crop ScienceBacteriamedicine.drug
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