Search results for "Anemia"

showing 10 items of 352 documents

Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2

2020

Fanconi anemia (FA) is a rare chromosomal instability syndrome with various clinical features and high cancer incidence. Despite being a DNA repair disorder syndrome and a frequently observed clinical hypersensitivity of FA patients towards ionizing radiation, the experimental evidence regarding the efficiency of radiation-induced DNA double-strand break (DSB) repair in FA is very controversial. Here, we performed a thorough analysis of the repair of radiation-induced DSBs in G1 and G2 in FA fibroblasts of complementation groups A, C, D1 (BRCA2), D2, E, F, G and P (SLX4) in comparison to normal human lung and skin fibroblasts. γH2AX, 53BP1, or RPA foci quantification after X-irradiation was…

DNA End-Joining RepairBiologyBiochemistryFanconi Anemia Complementation Group F ProteinHistonesRecombinases03 medical and health scienceschemistry.chemical_compound0302 clinical medicineFanconi anemiaChromosome instabilitymedicineHumansDNA Breaks Double-StrandedFanconi Anemia Complementation Group G ProteinMolecular BiologyCells Cultured030304 developmental biologyBRCA2 ProteinChromosome Aberrations0303 health sciencesFanconi Anemia Complementation Group A ProteinFanconi Anemia Complementation Group D2 ProteinX-RaysCell CycleFanconi Anemia Complementation Group C ProteinRecombinational DNA RepairChromosomeDNACell BiologyFibroblastsCell cyclemedicine.diseaseFanconi Anemia Complementation Group E ProteinComplementationKineticsenzymes and coenzymes (carbohydrates)Fanconi Anemiachemistry030220 oncology & carcinogenesisPremature chromosome condensationMutationCancer researchChromatidTumor Suppressor p53-Binding Protein 1DNADNA Repair
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Lentiviral-Mediated Gene Therapy in Fanconi Anemia-A Mice Reveals Long-Term Engraftment and Continuous Turnover of Corrected HSCs

2015

International audience; Fanconi anemia is a DNA repair-deficiency syndrome mainly characterized by cancer predisposition and bone marrow failure. Trying to restore the hematopoietic function in these patients, lentiviral vector-mediated gene therapy trials have recently been proposed. However, because no insertional oncogenesis studies have been conducted so far in DNA repair-deficiency syndromes such as Fanconi anemia, we have carried out a genome-wide screening of lentiviral insertion sites after the gene correction of Fanca-/- hematopoietic stem cells (HSCs), using LAM-PCR and 454-pyrosequencing. Our studies first demonstrated that transduction of Fanca-/- HSCs with a lentiviral vector d…

DNA RepairDNA repair[SDV]Life Sciences [q-bio]Genetic enhancementGenetic VectorsBiologymedicine.disease_causePolymerase Chain ReactionViral vectorCell LineMiceFanconi anemiaTransduction Genetichemic and lymphatic diseasesDrug DiscoveryGeneticsmedicineAnimalsMolecular BiologyGenetics (clinical)Mice KnockoutFanconi Anemia Complementation Group A ProteinLentivirusBone marrow failureGenetic Therapymedicine.diseaseHematopoietic Stem CellsFANCA3. Good health[SDV] Life Sciences [q-bio]Fanconi AnemiaCancer researchMolecular MedicineStem cellCarcinogenesis
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Oxidative stress in Fanconi anaemia: from cells and molecules towards prospects in clinical management.

2011

Abstract Fanconi anaemia (FA) is a genetic disease featuring bone marrow failure, proneness to malignancies, and chromosomal instability. A line of studies has related FA to oxidative stress (OS). This review attempts to evaluate the evidence for FA-associated redox abnormalities in the literature from 1981 to 2010. Among 2170 journal articles on FA evaluated, 162 related FA with OS. Early studies reported excess oxygen toxicity in FA cells that accumulated oxidative DNA damage. Prooxidant states were found in white blood cells and body fluids from FA patients as excess luminol-dependent chemiluminescence, 8-hydroxy-deoxyguanosine, reduced glutathione/oxidized glutathione imbalance, and tum…

DNA damageClinical BiochemistryBRIP1MitochondrionBiologymedicine.disease_causeBiochemistryFANCAPRDX3Oxidative StressFanconi AnemiaBiochemistryFANCGFANCD2Cancer researchmedicineAnimalsHumansMolecular BiologyOxidative stressBiological chemistry
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Impact of a Three Amino Acid Deletion in the CH2 Domain of Murine IgG1 on Fc-Associated Effector Functions

2008

Abstract Four murine IgG subclasses display markedly different Fc-associated effector functions because of their differential binding to three activating IgG Fc receptors (FcγRI, FcγRIII, and FcγRIV) and C1q. Previous analysis of IgG subclass switch variants of 34-3C anti-RBC monoclonal autoantibodies revealed that the IgG1 subclass, which binds only to FcγRIII and fails to activate complement, displayed the poorest pathogenic potential. This could be related to the presence of a three amino acid deletion at positions 233–235 in the CH2 domain uniquely found in this subclass. To address this question, IgG1 insertion and IgG2b deletion mutants at positions 233–235 of 34-3C anti-RBC Abs were …

Deletion mutantImmunologyAntibody AffinityDown-Regulationddc:616.07BiologySubclassProtein Structure Tertiary/geneticsMiceAnimalsImmunology and AllergyAmino AcidsEffector functionsSequence DeletionMice Knockoutchemistry.chemical_classificationMice Inbred BALB CMice Inbred NZBAnemia Hemolytic Autoimmune/genetics/immunologyReceptors IgGAutoantibodyAmino Acids/chemistry/genetics/metabolismIgg subclassesReceptors IgG/antagonists & inhibitors/genetics/metabolismPathogenicityProtein Structure TertiaryImmunoglobulin G/genetics/metabolismImmunoglobulin Switch RegionCell biologyAmino acidImmunoglobulin Heavy Chains/biosynthesis/genetics/metabolismAntibody Affinity/geneticsBiochemistrychemistryImmunoglobulin GMonoclonalMutagenesis Site-DirectedAnemia Hemolytic AutoimmuneDown-Regulation/genetics/immunologyImmunoglobulin Heavy ChainsThe Journal of Immunology
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Estudio epidemiológico de las parasitosis intestinales detectadas en la población infantil de Ruanda (África Central)

2016

La presente Tesis Doctoral tiene por objetivo conocer el estado del parasitismo intestinal y su correlación con diferentes factores intrínsecos y extrínsecos en la población infantil ruandesa. Para ello, se ha estudiado un total de 674 escolares (330 niños y 344 niñas) del Colegio Nemba I (Nemba, Gakenke, Província Norte de Ruanda), con edades comprendidas entre los 6 y 18 años de edad. Se ha detectado un espectro parasitario de 17 especies (10 de protozoos y 7 de helmintos), con una prevalencia total de parasitación del 94,9% (94,5% para protozoos y 18,1% para helmintos). Las especies más prevalentes fueron: Endolimax nana (91,1%), Blastocystis hominis (89,9%) y Entamoeba coli (57,2%). Se …

DesnutriciónÁfricaEnteroparásitosEosinofiliaAnemiaHelmintos:CIENCIAS MÉDICAS [UNESCO]:CIENCIAS DE LA VIDA [UNESCO]ProtozoosRuandaUNESCO::CIENCIAS MÉDICASUNESCO::CIENCIAS DE LA VIDAEpidemiologíaPrevalenciaPoblación infantil
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Diagnosis of chronic anaemia in gastrointestinal disorders: a guideline by the Italian Association of Hospital Gastroenterologists and Endoscopists (…

2019

Anaemia is a common pathologic condition, present in almost 5% of the adult population. Iron deficiency is the most common cause; other mechanisms can be involved, making anaemia a multi-factorial disorder in most cases. Anaemia being a frequent manifestation in the diseases of the gastrointestinal tract, patients are often referred to gastroenterologists. Furthermore, upper and lower endoscopy and enteroscopy are pivotal to the diagnostic roadmap of anaemia. In spite of its relevance in the daily clinical practice, there is a limited number of gastroenterological guidelines dedicated to the diagnosis of anaemia. For this reason, the Italian Association of Hospital Gastroenterologists and E…

EnteroscopyAdultmedicine.medical_specialtySettore MED/09 - Medicina InternaGastrointestinal DiseasesAdult populationAnaemiaInflammatory bowel diseaseEndoscopy Gastrointestinal03 medical and health sciences0302 clinical medicinePaediatric gastroenterologyhemic and lymphatic diseasesInternal medicinemedicineCeliac diseaseHumansIntensive care medicineChildSocieties MedicalHepatologyAnemia Iron-Deficiencybusiness.industryIron deficiencyGastroenterologyEndoscopyAnemiaGuidelineHepatologySmall bowelClinical PracticeChronic anaemiaItalyanaemia; celiac disease; endoscopy; h. pylori; inflammatory bowel disease; iron deficiency; small bowel030220 oncology & carcinogenesisAnaemia; Celiac disease; Endoscopy; H. pylori; Inflammatory bowel disease; Iron deficiency; Small bowel; Hepatology; Gastroenterology030211 gastroenterology & hepatologybusinessH. pyloriBiomarkers
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Markers of Anemia in Children with Type 1 Diabetes

2018

Aim. The aim of the study was to assess markers of anemia in type 1 diabetes (T1D) children, compare them to results obtained in the control group, and estimate their relation to BMI SDS. Methods. 94 (59% ♀) T1D children without other autoimmune disorders, aged 12.5 ± 4.1 years, T1D duration: 4.2 ± 3.6 years, HbA1c 7.3 ± 1.5% (57 ± 12.6 mmol/mol). Sex- and age-matched controls (43 children). In all children, anthropometric measurements, the blood count, iron turnover parameters, and vitamin B12 concentration were taken. Results. T1DM children had significantly higher red cell distribution width (RDW) (13.6 versus 12.6%; p<0.001), hepcidin (0.25 versus 0.12 ng/ml; p<0.001), and vitamin…

Erythrocyte IndicesMalemedicine.medical_specialtyArticle SubjectAdolescentAnemiaEndocrinology Diabetes and Metabolism030209 endocrinology & metabolismLogistic regressionlcsh:Diseases of the endocrine glands. Clinical endocrinologyGastroenterologyBody Mass IndexYoung Adult03 medical and health sciences0302 clinical medicineEndocrinologyHepcidinsHepcidin030225 pediatricsInternal medicinemedicineHumansVitamin B12ChildGlycated HemoglobinType 1 diabeteslcsh:RC648-665biologyMean corpuscular hemoglobin concentrationmedicine.diagnostic_testbusiness.industrynutritional and metabolic diseasesAnemiaRed blood cell distribution widthAnthropometrymedicine.diseaseBlood Cell CountVitamin B 12Diabetes Mellitus Type 1Child Preschoolbiology.proteinFemalebusinessBiomarkersResearch ArticleJournal of Diabetes Research
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Association of erythrocyte deformability with red blood cell distribution width in metabolic diseases and thalassemia trait.

2016

Abstract Increased red blood distribution width (RDW) in anemia is related to disturbances in the cellular surface/volume ratio, usually accompanied by morphological alterations, while it has been shown in inflammatory diseases that the activity of pro-inflammatory cytokines disturbing erythropoiesis increases RDW. Recently it has been reported that higher RDW is related with decreased erythrocyte deformability, and that it could be related with the association of RDW and increased risk of cardiovascular diseases. In order to analyze the influence of morphological alterations and proinflammatory status on the relationship between RDW and erythrocyte deformability, we analyzed erythrocyte de…

Erythrocyte IndicesMalemedicine.medical_specialtyErythrocytesPhysiologyAnemiaThalassemia030204 cardiovascular system & hematologyBiologyProinflammatory cytokine03 medical and health sciences0302 clinical medicinePhysiology (medical)Internal medicineErythrocyte DeformabilitymedicineErythrocyte deformabilityHumansMetabolic SyndromeRed blood cell distribution widthHematologymedicine.diseaseEndocrinology030220 oncology & carcinogenesisImmunologyErythrocyte CountErythropoiesisAnisocytosisThalassemiaMetabolic syndromeCardiology and Cardiovascular MedicineClinical hemorheology and microcirculation
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Crucial role of aspartic acid at position 265 in the CH2 domain for murine IgG2a and IgG2b Fc-associated effector functions.

2008

Abstract Replacement of aspartic acid by alanine at position 265 (D265A) in mouse IgG1 results in a complete loss of interaction between this isotype and low-affinity IgG Fc receptors (FcγRIIB and FcγRIII). However, it has not yet been defined whether the D265A substitution could exhibit similar effects on the interaction with two other FcγR (FcγRI and FcγRIV) and on the activation of complement. To address this question, 34-3C anti-RBC IgG2a and IgG2b switch variants bearing the D265A mutation were generated, and their effector functions and in vivo pathogenicity were compared with those of the respective wild-type Abs. The introduction of the D265A mutation almost completely abolished the…

ErythrocytesAspartic Acid/genetics/physiologyAntibodies Monoclonal/toxicityImmunologyMutantReceptors Fcddc:616.07Complement Activation/genetics/immunologyAlanine/geneticsMiceStructure-Activity RelationshipProtein structureImmunoglobulin G/chemistry/metabolismProtein Isoforms/chemistry/deficiency/genetics/physiologyAspartic acidImmunology and AllergyAnimalsProtein IsoformsErythrocytes/immunologyReceptorComplement ActivationAutoantibodiesAlanineMice KnockoutAspartic AcidMice Inbred BALB CAlaninebiologyAnemia Hemolytic Autoimmune/genetics/immunologyAntibodies MonoclonalReceptors Fc/chemistry/deficiency/genetics/physiologyFragment crystallizable regionIsotypeAmino Acid Substitution/genetics/physiologySialic Acids/geneticsProtein Structure TertiaryMice Inbred C57BLBiochemistryAmino Acid SubstitutionImmunoglobulin Gbiology.proteinSialic AcidsAutoantibodies/toxicityAnemia Hemolytic AutoimmuneAntibodyProtein Structure Tertiary/genetics/physiologyJournal of immunology (Baltimore, Md. : 1950)
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Anti-Eryptotic Activity of Food-Derived Phytochemicals and Natural Compounds

2022

Human red blood cells (RBCs), senescent or damaged due to particular stress, can be removed by programmed suicidal death, a process called eryptosis. There are various molecular mechanisms underlying eryptosis. The most frequent is the increase in the cytoplasmic concentration of Ca2+ ions, later exposure of erythrocytes to oxidative stress, hyperosmotic shock, ceramide formation, stimulation of caspases, and energy depletion. Phosphatidylserine (PS) exposed by eryptotic RBCs due to interaction with endothelial CXC-Motiv-Chemokin-16/Scavenger-receptor, causes the RBCs to adhere to vascular wall with consequent damage to the microcirculation. Eryptosis can be triggered by various xenobiotics…

ErythrocytesOrganic ChemistryPhytochemicalsEryptosisAnemiaGeneral MedicinePhosphatidylserinesRed blood cellsCatalysisPhenolic compoundsComputer Science ApplicationsInorganic ChemistryOxidative StressAlkaloidsSettore BIO/10 - BiochimicaFood-derived compoundAnimalsHumansCalciumPhysical and Theoretical ChemistryMolecular BiologySpectroscopy
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