Search results for "collage"

showing 10 items of 638 documents

A comparison of spreading and motility behaviour of 8701-BC breast carcinoma cells on type I, I-trimer and type V collagen substrata. Evidence for a …

1991

Ductal infiltrating carcinoma (d.i.c.) of human breast is a highly invasive neoplasm characterized by enhanced deposition of collagen. Paradoxically, enhanced collagen deposition is not correlated with inhibition of the migration of tumour cells into the host tissue. d.i.c. is characterized by the reappearance of ‘embryonic’ type I-trimer collagen and an increase in type V collagen content in the matrix. The effects of these two collagen types were compared with type I collagen as culture substrata on the spreading pattern, cytoskeletal organization and motile behaviour of 8701-BC breast carcinoma cells using rhodamine-phalloidin staining, a DNAase I-competition assay, scanning electron mic…

PhotomicrographyStromal cellVideotape RecordingMotilityBreast NeoplasmsTrimerCell BiologyMatrix (biology)BiologyActinsCulture MediaExtracellular MatrixCell biologyCollagen type I alpha 1Carcinoma Intraductal NoninfiltratingCell MovementCell cultureImmunologyTumor Cells CulturedHumansCollagenNeoplasm MetastasisCytoskeletonType I collagenJournal of Cell Science
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Type V collagen regulates the expression of apoptotic and stress response genes by breast cancer cells.

2004

Type V collagen is a "minor" component of normal human breast stroma, which is subjected to over-deposition in cases of ductal infiltrating carcinoma (DIC). We reported that, if used as a culture substrate for the DIC cell line 8701-BC, it exhibited poorly-adhesive properties and restrained the proliferative and motile behavior of the cell subpopulation able to attach onto it. Moreover, this collagen species was able to trigger DNA fragmentation and impair survival of 8701-BC cells. In this study, we have extended our investigation with the aim to obtain further evidence that the death induced by type V collagen was of the apoptotic type by (i) microscopic detection and quantitation of Apop…

PhysiologyClinical BiochemistryCellApoptosisBreast NeoplasmsEnzyme activatorCell Line TumormedicineHumansSettore BIO/06 - Anatomia Comparata E CitologiaCaspaseHeat-Shock ProteinsbiologyCarcinoma Ductal BreastCell BiologyMolecular biologyIn vitroEnzyme ActivationGene Expression Regulation Neoplasticmedicine.anatomical_structurecollagen breast cancer gene expressionApoptosisCell cultureCaspasesbiology.proteinDNA fragmentationHSP60FemaleCollagen Type VJournal of cellular physiology
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Activation of the first component of complement, C1: comparison of the effect of sixteen different enzymes on serum C1.

1983

In this study, the effect of sixteen different enzymes on serum C1 and its subcomponents was investigated. The sixteen enzymes could be divided into three groups. First, enzymes which activate native C1: trypsin (optimal concentration 2.4 x 10(-4) mM); alpha-chymotrypsin (2.3 x 10(3) mM); thrombin (1.0 x 10(-5) mM); plasmin (1.9 x 10(-5) mM); elastase (5.8 x 10(-5) mM); pronase (3.0 x 10(-6) mM). All these enzymes are serine esterase and activate native serum C1 bound to EAC4 at the given concentration within 10 min at 30 degrees C. Furthermore, native C1 inhibited by a pentosanpolysulfoester, Sp54, is unable to undergo the internal activation but can be externally activated by the serine e…

PlasminComplement Activating EnzymesImmunologyGuinea PigsDose-Response Relationship ImmunologicPronaseSerinechemistry.chemical_compoundComplement C1medicineImmunology and AllergyAnimalsHumansTrypsinFibrinolysinComplement Activationchemistry.chemical_classificationPentosan Sulfuric PolyesterbiologyHematologyTrypsinCarboxypeptidaseKineticsEnzymeBiochemistrychemistrybiology.proteinCollagenaseCattleRabbitsLysozymemedicine.drugPeptide HydrolasesImmunobiology
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SPIONs embedded in polyamino acid nanogels to synergistically treat tumor microenvironment and breast cancer cells.

2018

Abstract The extremely complex tumor microenvironment (TME) in humans is the major responsible for the therapeutic failure in cancer nanomedicine. A new concept of disease-driven nanomedicine, henceforth named “Theranomics”, which attempts to target cancer cells and TME on the whole, represents an attractive alternative. Herein, a nanomedicine able to co-deliver doxorubicin and a tumor suppressive proteolytic protein such as collagenase-2 was developed. We successfully obtained superparamagnetic nanogels (SPIONs/Doco@Col) via the intermolecular azide-alkyne Huisgen cycloaddition. We demonstrated that a local ECM degradation and remodeling in solid tumors by means of collagenase-2 could enha…

Polyamino acidPolyamino acidsCollagenasePharmaceutical ScienceBreast Neoplasms02 engineering and technology030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineBreast cancerBreast cancerDrug Delivery SystemsCell Line TumormedicineTumor MicroenvironmentHumansDoxorubicinTargeted cancer therapyAmino AcidsMagnetite NanoparticlesTumor microenvironmentAntibiotics AntineoplasticChemistrySPIONCancerTheranomicDrug Synergism021001 nanoscience & nanotechnologymedicine.diseasenanomedicineNanomedicinesDrug LiberationSPIONsMatrix Metalloproteinase 8DoxorubicinCancer cellCancer researchNanomedicineTheranomicsFemaleBreast cancer cellspolyamino acid0210 nano-technologyGelsmedicine.drugInternational journal of pharmaceutics
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Influence of scaffold pore size on collagen I development: A new in vitro evaluation perspective

2013

Bone tissue engineering takes part in the complex process of bone healing by combining cells, chemical/physical signals, and scaffolds with the scaffolds providing an artificial extracellular matrix network. The role of the support template for cell activity is crucial to guide the healing process. This in vitro study compared three different poly(D,L-lactic acid) scaffolds obtained by varying the pore size generated by applying different salt leaching processes. The influence of pore dimensions on the extracellular matrix produced by human osteosarcoma-derived osteoblasts (MG63 cell line) seeded on these different materials was analyzed. This study is targeted on the intermediate stage of…

Pore sizeScaffoldPolymers and PlasticsChemistryConfocalBioengineeringBone healingIn vitroBiomaterialsExtracellular matrixGene expressionCollagen networkMaterials ChemistryBiomedical engineeringJournal of Bioactive and Compatible Polymers
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Blood absorption capacity of different xenograft bone substitutes. An in-vitro study

2019

Background Commercially available xenograft blocks, claim to have adequate characteristics to interact with biological media and thus permitting biological fluid absorption. The objective of this in vitro study was to compare the blood absorption capacity of four different xenograft block materials of different composition of collagen and porosity. Material and Methods Four brands of xenograft block materials were used (NuOss®, Bio-Oss®, Osteobiol® and Smartbone®). Five samples of each brand were analyzed, making a total of 20 tests. Human blood was used as the absorption liquid for the present experiment. The time period, in which the block remains in contact with the blood, was registered…

Porosidad616.3Absorption (skin)Regeneració òssiaOsteoconductionBiological fluidOsteoconducción03 medical and health sciences0302 clinical medicineAbsorción de sangreBiomaterials and Bioengineering in DentistryXenoinjertoIn vitro studyXenoinjertsRegeneración óseaBone regenerationGeneral DentistryCol·lagenXenograftsPorositatChemistryResearchSignificant differenceBiomaterialSmall sample030206 dentistry:CIENCIAS MÉDICAS [UNESCO]Bone regeneration030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASAbsorption capacityOsteoconduccióColágenoCollagenPorosityBiomedical engineeringAbsorció de sangBlood absorption
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Autofluorescence imaging of basal cell carcinoma by smartphone RGB camera

2015

The feasibility of smartphones for in vivo skin autofluorescence imaging has been investigated. Filtered autofluorescence images from the same tissue area were periodically captured by a smartphone RGB camera with subsequent detection of fluorescence intensity decreasing at each image pixel for further imaging the planar distribution of those values. The proposed methodology was tested clinically with 13 basal cell carcinoma and 1 atypical nevus. Several clinical cases and potential future applications of the smartphone-based technique are discussed.

PorphyrinsSkin NeoplasmsLightComputer scienceBiomedical EngineeringDermoscopyImage processingFluorescenceBiomaterialsOpticsmedicineHumansBasal cell carcinomaNevusSkinPhotobleachingPixelbusiness.industrySkin autofluorescenceNADmedicine.diseaseAtypical nevusAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsAutofluorescenceFluorescence intensityMicroscopy FluorescenceCarcinoma Basal CellRGB color modelCollagenSmartphonebusinessBiomedical engineeringJournal of Biomedical Optics
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The New Dense-city tra Collage City e Citta Analoga

2012

The Prin 2007 research project of the Palermo Unit. The New Dense-city between Collage City e Analogous Town. In the introductory paper submitted by the Palermo Unit, Andrea Sciascia transforms the results reached in the incipit allowing us to assess the entire path followed by the research excursus. A thorough examination has been carried out on the final plans, the so-called recompositions stemming from the the merging of a number of projects on the two neighbourhoods under study: Borgo Ulivia and ZEN. The reflection starts from a specific verb: densifying. The suburban fabric of the two neighbourhoods becomes more dense by adding those missing facilities, but especially by re-establishin…

Progettare PeriferiaCollage City e Citta AnalogaSettore ICAR/14 - Composizione Architettonica E Urbana
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Apoptosis causes lumen formation during angiogenesis in vitro.

2002

Programmed cell deathUmbilical VeinsAngiogenesisLumen (anatomy)ApoptosisBiologyBiochemistryUmbilical veinmedicineIn Situ Nick-End LabelingHumansCells CulturedNeovascularization PathologicCell BiologyIntercellular Adhesion Molecule-1ImmunohistochemistryIn vitroCell biologyEndothelial stem cellPlatelet Endothelial Cell Adhesion Molecule-1Microscopy Electronmedicine.anatomical_structureApoptosisImmunologyCollagenEndothelium VascularCardiology and Cardiovascular MedicineBlood vesselMicrovascular research
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The interaction of recombinant subdomains of the procollagen C-proteinase with procollagen I provides a quantitative explanation for functional diffe…

2006

The procollagen C-proteinase (PCP) is a zinc peptidase of the astacin family and the metzincin superfamily. The enzyme removes the C-terminal propeptides of fibrillar procollagens and activates other matrix proteins. Besides its catalytic protease domain, the procollagen C-proteinase contains several C-terminal CUB modules (named after complement factors C1r and C1s, the sea urchin UEGF protein, and BMP-1) and EGF-like domains. The two major splice forms of the C-proteinase differ in their overall domain composition. The longer variant, termed mammalian tolloid (mTld, i.e., PCP-2), has the protease- CUB1-CUB2-EGF1-CUB3-EGF2-CUB4-CUB5 composition, whereas the shorter form termed bone morphog…

ProteasesProtein FoldingTolloid-Like Metalloproteinasesmedicine.medical_treatmentRNA SplicingBiologyAntiparallel (biochemistry)BiochemistryBone morphogenetic protein 1law.inventionBone Morphogenetic Protein 1lawmedicineAnimalsProtein precursorDNA PrimersProteaseBase SequenceCircular DichroismMetalloendopeptidasesSurface Plasmon ResonanceRecombinant ProteinsProcollagen peptidaseSpectrometry FluorescenceBiochemistryBone Morphogenetic ProteinsRecombinant DNAMetalloproteasesElectrophoresis Polyacrylamide GelAstacinProcollagenBiochemistry
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