Search results for "Epigenomics"

showing 10 items of 78 documents

The first European interdisciplinary ewing sarcoma research summit.

2012

This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License.-- et al.

EpigenomicsCancer ResearchAlternative medicineMedizinComputingMilieux_LEGALASPECTSOFCOMPUTINGReview ArticleBioinformatics[SDV.BBM.BM] Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologydrug screen0302 clinical medicineDrug screenCancer genomicssignallingSarcomagenesis0303 health sciencessarcomagenesisSummitgeography.geographical_feature_categoryOpinion leadershipGenomicsLaboratory resultslcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogensPrognosisanimal models3. Good healthAnimal modelsMetastatic Ewing SarcomaOncology030220 oncology & carcinogenesis[SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]EpigeneticsSarcomaImmunotherapyPrioritizationmedicine.medical_specialty[SDV.CAN]Life Sciences [q-bio]/Cancerlcsh:RC254-28203 medical and health sciences[SDV.CAN] Life Sciences [q-bio]/Cancer[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]medicinegenomics030304 developmental biologyMedical educationgeographyepigeneticsbusiness.industrybiomarkers[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry Molecular Biology/Molecular biologymedicine.diseaseClinical trialprognosisbusinessBiomarkersEwing sarcomaFrontiers in oncology
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Astrocytes and neurons share region-specific transcriptional signatures that confer regional identity to neuronal reprogramming

2021

Region-specific gene expression shared with neurons imparts to astrocytes competence for region-specific neuronal reprogramming.

EpigenomicsCellThalamusNeocortexBiology03 medical and health sciences0302 clinical medicineThalamusGene expressionmedicineEpigeneticsProgenitor cellNeural cellResearch Articles030304 developmental biologyNeurons0303 health sciencesMultidisciplinaryNeocortexSciAdv r-articlesmedicine.anatomical_structurenervous systemAstrocytesNeuroscienceReprogramming030217 neurology & neurosurgeryResearch ArticleNeuroscience
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Epigenetic biomarkers: A new perspective in laboratory diagnostics.

2012

Epigenetics comprises the study of chemical modifications in the DNA and histones that regulates the gene expression or cellular phenotype. However, during the last decade this term has evolved after the elucidation of different mechanisms (microRNAs and nuclear organization of the chromosomes) involved in regulating gene expression. Epigenetics and the new designed technologies capable to analyze epigenetic changes (e.g., methylated DNA, miRNAs expression, post-translational modifications on histones among others) have disclosed an appealing scenario that will offer for the biomedical sciences new biomarkers for the study of neurodegenerative diseases, multifactorial complex diseases, rare…

EpigenomicsClinical BiochemistryBiologyBiochemistryEpigenesis GeneticHistonesmicroRNACancer; DNA methylation; Histone; MiRNAs; Rare disease;HumansEpigeneticsPathology MolecularEpigenesisEpigenomicsCancerGeneticsEpigenetic biomarkersBiochemistry (medical)Nuclear organizationGeneral MedicineSequence Analysis DNADNA MethylationHistoneMicroRNAsHistoneDNA methylationbiology.proteinMiRNAsRare diseaseProtein Processing Post-TranslationalBiomarkersClinica chimica acta; international journal of clinical chemistry
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Value of genetic and epigenetic testing as biomarkers of response to antidepressant treatment

2013

Major depressive disorder (MDD) is one of the most prevalent and disabling psychiatric disorders worldwide and therefore an important public health priority. The selection process of antidepressant treatment is primarily guided by trial and error, and the outcomes with current antidepressant strategies are disappointing. The biological background of the disease is heterogeneous with presumably multiple biological systems involved. With the aim to individualize antidepressant treatment, multiple candidate gene and a few genome-wide association studies have been performed, but so far with very limited success. To address the dynamic changes of depressive symptoms and their response to treatme…

EpigenomicsDepressive Disorder Majormedicine.medical_specialtyCandidate genemedicine.diagnostic_testDiseasemedicine.diseaseAntidepressive AgentsPsychiatry and Mental healthPharmacogeneticsmedicineHumansBiomarker (medicine)Major depressive disorderAntidepressantGenetic TestingPsychologyPsychiatryBiomarkersPharmacogeneticsEpigenomicsGenetic testingInternational Review of Psychiatry
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Losing DNA methylation at repetitive elements and breaking bad

2021

Abstract Background DNA methylation is an epigenetic chromatin mark that allows heterochromatin formation and gene silencing. It has a fundamental role in preserving genome stability (including chromosome stability) by controlling both gene expression and chromatin structure. Therefore, the onset of an incorrect pattern of DNA methylation is potentially dangerous for the cells. This is particularly important with respect to repetitive elements, which constitute the third of the human genome. Main body Repetitive sequences are involved in several cell processes, however, due to their intrinsic nature, they can be a source of genome instability. Thus, most repetitive elements are usually meth…

EpigenomicsGenome instabilityHeterochromatinSatellitesReviewRepetitive DNABiologyQH426-47003 medical and health sciencesLINE-10302 clinical medicineDNA hypomethylationGeneticsHumansEpigeneticsAutism spectrum disorderRepeated sequenceMolecular BiologyRepetitive Sequences Nucleic Acid030304 developmental biologyCancerGenetics0303 health sciencesHereditary diseasesDNA MethylationChromatinChromatinSettore BIO/18 - GeneticaLong Interspersed Nucleotide ElementsICF syndromeDNA methylationHuman genomeAlzheimer’s disease030217 neurology & neurosurgeryNeuropsychiatric disordersDNA hypomethylationEpigenetics & Chromatin
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Genome-wide promoter methylation analysis in neuroblastoma identifies prognostic methylation biomarkers.

2012

Background: Accurate outcome prediction in neuroblastoma, which is necessary to enable the optimal choice of risk-related therapy, remains a challenge. To improve neuroblastoma patient stratification, this study aimed to identify prognostic tumor DNA methylation biomarkers.Results: To identify genes silenced by promoter methylation, we first applied two independent genome-wide methylation screening methodologies to eight neuroblastoma cell lines. Specifically, we used re-expression profiling upon 5-aza-2'-deoxycytidine (DAC) treatment and massively parallel sequencing after capturing with a methyl-CpG-binding domain (MBD-seq). Putative methylation markers were selected from DAC-upregulated …

EpigenomicsMYCN Single CopyMedizinPrimary Neuroblastoma TumorBioinformaticsNeuroblastoma0302 clinical medicineRisk FactorsMYCN StatusDatabases GeneticPromoter MethylationGTP-Binding Protein alpha Subunits GsHazard Ratio PatientPromoter Regions GeneticEpigenomicsRegulation of gene expression0303 health sciencesMassive parallel sequencingHigh-Throughput Nucleotide SequencingMethylation3. Good healthGene Expression Regulation NeoplasticMedizinische Fakultät » Universitätsklinikum Essen » Zentrum für Kinder- und Jugendmedizin030220 oncology & carcinogenesisDNA methylationAzacitidineBiologieBiologyDecitabine03 medical and health sciencesneuroblastomaCell Line TumorNeuroblastomaBiomarkers TumorChromograninsmedicineHumansddc:61ddc:610Epigenetics030304 developmental biologyepigeneticsGenome HumanResearchBiology and Life SciencesbiomarkersSequence Analysis DNADNA MethylationHCT116 Cellsmedicine.diseaseSurvival AnalysisCancer researchHuman genomeDNA-methylation
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Blood and skeletal muscle ageing determined by epigenetic clocks and their associations with physical activity and functioning

2021

AbstractThe aim of this study was to investigate the correspondence of different biological ageing estimates (i.e. epigenetic age) in blood and muscle tissue and their associations with physical activity (PA), physical function and body composition. Two independent cohorts (N = 139 and N = 47) were included, whose age span covered adulthood (23–69 years). Whole blood and m. vastus lateralis samples were collected, and DNA methylation was analysed. Four different DNA methylation age (DNAmAge) estimates were calculated using genome-wide methylation data and publicly available online tools. A novel muscle-specific methylation age was estimated using the R-package ‘MEAT’. PA was measured with q…

EpigenomicsMale0301 basic medicineAgingmaximal oxygen consumptionbiological ageingMonozygotic twinPhysiologyEpigenesis GeneticCohort Studies0302 clinical medicinetwin studyGenetics (clinical)Whole blood0303 health sciencesDNA methylationDual-energy X-ray absorptiometryTwin studyMiddle AgedDNA-metylaatiomedicine.anatomical_structuremuscle massepigenetiikkaDNA methylationFemaledual-energy X-ray absorptiometryAdultMuscle tissueBiologyYoung Adult03 medical and health sciencesMaximal oxygen consumptionmaksimaalinen hapenottoGeneticsmedicineHumansEpigeneticsMuscle SkeletalExerciseMolecular BiologyAged030304 developmental biologykaksostutkimusMuscle strengthResearchSkeletal muscleMuscle massCardiorespiratory fitnessBiological ageingTwin studyikääntyminen030104 developmental biologylihasmassaAgeing3121 General medicine internal medicine and other clinical medicinemuscle strength030217 neurology & neurosurgerylihasvoimaDevelopmental BiologyClinical Epigenetics
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Epigenomics and metabolomics reveal the mechanism of the APOA2-saturated fat intake interaction affecting obesity

2018

BACKGROUND: The putative functional variant −265T>C (rs5082) within the APOA2 promoter has shown consistent interactions with saturated fatty acid (SFA) intake to influence the risk of obesity. OBJECTIVE: The aim of this study was to implement an integrative approach to characterize the molecular basis of this interaction. DESIGN: We conducted an epigenome-wide scan on 80 participants carrying either the rs5082 CC or TT genotypes and consuming either a low-SFA (C genotype, promoting an APOA2 expression difference between APOA2 genotypes on a high-SFA diet, and modulating BCAA and tryptophan metabolic pathways. These findings identify potential mechanisms by which this highly reproducible ge…

EpigenomicsMale0301 basic medicineGenotypeMedicine (miscellaneous)030204 cardiovascular system & hematologyBiologyBioinformatics03 medical and health sciences0302 clinical medicineFramingham Heart StudyMetabolomicsGenotypemedicineHumansMetabolomicsDrug InteractionsObesityEpigeneticsAgedEpigenomicsNutrition and DieteticsApolipoprotein A-Ifood and beveragesGenetic VariationEpigenomeDNA MethylationMiddle AgedLipid Metabolismmedicine.diseaseDietary FatsObesityOriginal Research Communications030104 developmental biologyGene Expression RegulationSaturated fatty acidCpG IslandsFemaleApolipoprotein A-IIThe American Journal of Clinical Nutrition
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Science and Healthy Meals in the World: Nutritional Epigenomics and Nutrigenetics of the Mediterranean Diet

2020

The Mediterranean Diet (MD), UNESCO Intangible Cultural Heritage of Humanity, has become a scientific topic of high interest due to its health benefits. The aim of this review is to pick up selected studies that report nutrigenomic or nutrigenetic data and recapitulate some of the biochemical/genomic/genetic aspects involved in the positive health effects of the MD. These include (i) the antioxidative potential of its constituents with protective effects against several diseases; (ii) the epigenetic and epigenomic effects exerted by food components, such as Indacaxanthin, Sulforaphane, and 3-Hydroxytyrosol among others, and their involvement in the modulation of miRNA expression; (iii) the …

EpigenomicsMale0301 basic medicineIntangible cultural heritageMediterranean dietHealth StatusGene Expressionlcsh:TX341-641030209 endocrinology & metabolismReviewnutrigenomicHealth benefitsBiologyDiet MediterraneanXanthineAntioxidantsNutrigeneticsEating03 medical and health sciences0302 clinical medicinenutrigenomicsIsothiocyanatesSettore BIO/10 - BiochimicaMediterranean dietEnvironmental healthHumansFood componentsSettore BIO/06 - Anatomia Comparata E CitologianutrigeneticsEpigenomics030109 nutrition & dieteticsNutrition and DieteticsCooking methodsPhenylethyl AlcoholMicroRNAsSettore BIO/18 - GeneticaNutrigenomicsNutrigeneticSulfoxidesFemaleDiet Healthylcsh:Nutrition. Foods and food supplyFood AnalysisFood ScienceNutrients
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Metabolic and Vascular Effect of the Mediterranean Diet

2019

Several studies indicated how dietary patterns that were obtained from nutritional cluster analysis can predict disease risk or mortality. Low-grade chronic inflammation represents a background pathogenetic mechanism linking metabolic risk factors to increased risk of chronic degenerative diseases. A Mediterranean diet (MeDi) style has been reported as associated with a lower degree of inflammation biomarkers and with a protective role on cardiovascular and cerebrovascular events. There is heterogeneity in defining the MedDiet, and it can, owing to its complexity, be considered as an exposome with thousands of nutrients and phytochemicals. Recently, it has been reported a novel positive ass…

EpigenomicsMale0301 basic medicineMediterranean dietPhysiologyBlood lipidsBlood PressureReview030204 cardiovascular system & hematologyDiet MediterraneanBody Mass IndexEpigenesis Geneticlcsh:ChemistryTranscriptome0302 clinical medicineMedicinelcsh:QH301-705.5SpectroscopyRandomized Controlled Trials as TopicEpigenomicsIncidenceGeneral MedicineLipidLipidsComputer Science ApplicationsFemaledietary patternWaist CircumferenceHumancardiovascular riskExposomeEpigenomicCatalysisInorganic Chemistry03 medical and health sciencesDiabetes mellitusHumansPhysical and Theoretical ChemistryMolecular BiologyAgedHeart Failurebusiness.industryMechanism (biology)Organic Chemistrymediterranean dietBiomarkermedicine.disease030104 developmental biologylcsh:Biology (General)lcsh:QD1-999businessBody mass indexBiomarkersInternational Journal of Molecular Sciences
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