FerroReg
Identification and functional characterization of extracellular and intracellular genetic regulators of ferroptosis related processes in multiple sclerosis
Akronim / šifra: FerroReg / 7753406NIO nosilac projekta: Univerzitet u Beogradu - Institut za nuklearne nauke „Vinča“
NIO učesnici projekta: Medical Faculty of the Military Medical Academy, University of Defence in Belgrade, Serbia; University of Belgrade, Institute for Medical Research, National Institute of Republic of Serbia
Rukovodilac projekta: Maja Živković, naučni savetnik
Website projekta: https://ferroreg.vin.bg.ac.rs/
Projekat finansira: Fond za nauku Republike Srbije
Program: IDEJE
Period realizacije: 2022 - 2025.
[en] FerroReg will provide entirely new knowledge/evidence of intracellular (mRNA, miRNA, SNPs) and extracellular (exosomes) transcriptional and post-transcriptional regulation and association with metabolic indicators of the ferroptosis key processes in human disease. Multiple sclerosis, a chronic inflammatory and neurodegenerative disease with no current cure, in its etiology comprehend: increased susceptibility of CNS to oxidative damage, and mitochondrial dysfunction, impaired iron metabolism, which all lead to accumulation of lipid peroxidation products, a main driving force for ferroptosis. MS is one of leading lifelong chronic disease with neurological, cognitive and physical disability, common in young adults. Therapeutic capacities to modulate ferroptosis, recently discovered cell death, have been highlighted, in vitro, and require further research to complement lack of studies in humans. Project will integrate genetics, bioinformatics and biochemical methodology in biomedical research in humans, using high-end methodology, next-generation sequencing, gas chromatography, qPCR, and analytical methods to provide multilevel molecular data. Project will impact implementation of the Strategy of scientific and technological development of the RS (RIS3). New knowledge on the genotype-phenotype interactions and cell to cell genetic remote regulators will impact scientific excellence and relevance, therapeutic capacities, public health actions and strategies, pairing of science and scientific community with social awareness and responsibility.
Najnovije
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Association of Functional Gene Variants in DYSF–ZNF638, MTSS1 and Ferroptosis-Related Genes with Multiple Sclerosis Severity and Target Gene Expression
(International Journal of Molecular Sciences, 2025) -
The genetic pathways of ferroptosis-related processes in multiple sclerosis
(University of Belgrade : Institute of Molecular Genetics and Genetic Engineering, 2024) -
Exploring Genetic Variant Selection Algorithms for Enhanced Genotyping Assays in Personalized Medicine
(University of Belgrade : Institute of Molecular Genetics and Genetic Engineering, 2024) -
Targeted RNAseq Revealed the Gene Expression Signature of Ferroptosis-Related Processes Associated with Disease Severity in Patients with Multiple Sclerosis
(International Journal of Molecular Sciences, 2024) -
The crosstalk between circulating exosome carried miRNAs and ferroptosis related genes in multiple sclerosis
(Serbian Society for Extracellular Vesicles (SrbEVs), Austrian Society for Extracellular Vesicles (ASEV), Hungarian Section for Extracellular Vesicles (HSEV), Slovenian Netvork for Extracellular Vesicles (SiN-EV), 2023) -
Capacity of fullerenols to modulate neurodegeneration induced by ferroptosis: Focus on multiple sclerosis
(Multiple Sclerosis and Related Disorders, 2025) -
Fatty Acid Profiles Differ Between Healthy and Multiple Sclerosis-Diagnosed Adults
(Belgrade : Serbian Society for Mitochondrial and Free Radical Physiology, 2024) -
Circulatory Indicators of Lipid Peroxidation, the Driver of Ferroptosis, Reflect Differences between Relapsing–Remitting and Progressive Multiple Sclerosis
(International Journal of Molecular Sciences, 2024) -
Bioinformatic analysis predicts serum EV miRNA hsa-miR-378a-3p as potential downregulator of Ceramide signaling pathway in peripheral blood CD8+ T cells of glioblastoma patients
(Serbian Society for Extracellular Vesicles : Austrian Society for Extracellular Vesicles : Baltic Society for Extracellular Vesicles : Italian Society for Extracellular Vesicles : French Society for Extracellular Vesicles : Spanish Society for Extracellular Vesicles : German Society for Extracellular Vesicles : United Kingdom Society for Extracellular Vesicles, 2024) -
Cargo of circulating extracellular vesicles regulates CDKN1A gene expression according to the MS disease severity
(Serbian Society for Extracellular Vesicles : Austrian Society for Extracellular Vesicles : Baltic Society for Extracellular Vesicles : Italian Society for Extracellular Vesicles : French Society for Extracellular Vesicles : Spanish Society for Extracellular Vesicles : German Society for Extracellular Vesicles : United Kingdom Society for Extracellular Vesicles, 2024) -
Association of genetic variant RS3176326 residing in ferroptosis-related CDKN1A with multiple sclerosis severity
(Belgrade : Serbian Genetic Society, 2024) -
Ferroptosis-related processes gene expression and gene variants: relevance for disease severity in patients with multiple sclerosis
(Belgrade : Serbian Genetic Society, 2024) -
Essential trace element levels in multiple sclerosis: bridging demographic and clinical gaps, assessing the need for supplementation
(Journal of Trace Elements in Medicine and Biology, 2024) -
FADS2 gene variant rs174593 is associated with multiple sclerosis
(CoMBoS2 – the Second Congress of Molecular Biologists of Serbia : Book of abstracts, 2023) -
Insight in miRNome of severe multiple sclerosis: Pilot study of distinctive relapse-onset MS phenotypes
(17th World Congress on Controversies in Neurology (CONy) : e-posters, 2023) -
Leptin signalling genetic variants and insulin resistance in multiple sclerosis patients
(CONy : 17th World Congress on Controversies in Neurology : Abstract book, 2023)
