{"database":"ENA","file_versions":[],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Histology and Embriology, Poznan University of Medical Science"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA663888"],"scientific_name":["Homo sapiens"],"long_description":["Human induced pluripotent stem cells (hiPSCs) possess the ability to differentiate into chondrocytes and produce cartilaginous matrix without the need to biopsy healthy cartilage. However, this strategy is not without risk given that those transplanted cells can be subjected to IR during Head and Neck (H&N) (re-)treatment. The main aim of this study was to investigate the microRNA expression profile after ionizing radiation (IR) treatment of chondrocyte-like cells differentiated from hiPSCs. The differentiated hiPSC into chondrocyte were irradiated in accordance with conventional therapy, hypofractionation and hyperfractionation protocols (1, 2, 3 Gy) intended for larynx region. Then, to fulfill specific objective we performed following high-throughput analysis: gene expression profile based on microarrays. Our findings allowed for the selection of crucial biological processes activated in hiPSC-derived chondrocytes after IR. Moreover, we observed decrease of expression of genes involved in e.g. cell cycle and cell division. Next, we have selected crucial microRNAs which are responsible for controlling genes of aforementioned biological processes. Microarray data were confirmed by RT-qPCR technique. We have proved that IR have a great impact on DDR mechanisms of hiPSCs differentiated towards chondrogenic lineage. Overall design: To irradiate the chondrocyte-like cells the specially modified and redesigned the Alderson Radiation Therapy phantom (ART) was used to obtain similar condition to those in patient’s larynx region treatment. Eppendorf tube with the one million of chondrocyte-like cells was used to irradiate the cells and was delineated as the quasi-Gross tumor volume (GTV), defining 1 cm geometrical margins around GTV to create the quasi-Clinical Target Volume (CTV) was done. The miRNA-enriched fraction from hiPSCs after chondrogenic differentiation were purified with miRNeasy Kit and RNeasy MinElute according to the manufacturer’s instructions (217004, Quiagen, Hilden, Germany)."],"tag":["xref:PubMed:33820914"],"repository":["ENA"],"description_synonyms":["Therapy, RNA, Chondrocyte, Chemotactic, human being, Materials, postnatal development., Fibroblast-Derived IPS Cell, Induced Pluripotent Stem Cell, IPS, stRNA, Chemotactic Cytokines, Modern, Small Temporal RNA, Fibroblast Derived IPS Cells, Gene, hiPSC, growth and development, Primary, Cistrons, IPS Cells, Cell, Human, development, Small, Cytokines, Micro RNA, Cytokine, Homo sapiens, Fibroblast Derived Induced Pluripotent Stem Cells, Chemokine, Genetic Materials, Intercrines, Intercrine, pre-miRNA, Man, IPS Cell, Chemotactic Cytokine, Genetic Material, Chondroblast, pri miRNA, Radiations, treatment, cartilage cell, Fibroblast-Derived IPS Cells, miRNAs, Small Temporal, Man (Taxonomy), Genetic, Micro, growth pattern, Temporal RNA, non-developmental growth, Fibroblast-Derived IPS, postnatal growth, Primary MicroRNA, INSDC_feature:gene, miRNA, Primary miRNA, Fibroblast-Derived, INSDC_feature:ncRNA, pri-miRNA, Treatments, human, Human Induced Pluripotent Stem Cells, Chondroblasts, Therapeutic, Material, Modern Man, Cells, disease management, Fibroblast-Derived Induced Pluripotent Stem Cells, Therapies, MicroRNA, Treatment, Cistron, Human Induced Pluripotent Stem Cell, growth, pre miRNA"],"name_synonyms":["Therapy, RNA, Chondrocyte, Chemotactic, human being, Materials, postnatal development., Fibroblast-Derived IPS Cell, Induced Pluripotent Stem Cell, IPS, stRNA, Chemotactic Cytokines, Modern, Small Temporal RNA, Fibroblast Derived IPS Cells, Gene, hiPSC, growth and development, Primary, Cistrons, IPS Cells, Cell, Human, development, Small, Cytokines, Micro RNA, Cytokine, Homo sapiens, Fibroblast Derived Induced Pluripotent Stem Cells, Chemokine, Genetic Materials, Intercrines, Intercrine, pre-miRNA, Man, IPS Cell, Chemotactic Cytokine, Genetic Material, Chondroblast, pri miRNA, Radiations, treatment, cartilage cell, Fibroblast-Derived IPS Cells, miRNAs, Small Temporal, Man (Taxonomy), Genetic, Micro, growth pattern, Temporal RNA, non-developmental growth, Fibroblast-Derived IPS, postnatal growth, Primary MicroRNA, INSDC_feature:gene, miRNA, Primary miRNA, Fibroblast-Derived, INSDC_feature:ncRNA, pri-miRNA, Treatments, human, Human Induced Pluripotent Stem Cells, Chondroblasts, Therapeutic, Material, Modern Man, Cells, disease management, Fibroblast-Derived Induced Pluripotent Stem Cells, Therapies, MicroRNA, Treatment, Cistron, Human Induced Pluripotent Stem Cell, growth, pre miRNA"],"additional_accession":[]},"is_claimable":false,"name":"microRNA from Ionizing radiation treatment of chondrocyte-like cells derived from human induced pluripotent stem cells: gene and microRNA expression profile and high-throughput screening of secreted cytokines, chemokines, and growth factors","description":"microRNA from Ionizing radiation treatment of chondrocyte-like cells derived from human induced pluripotent stem cells: gene and microRNA expression profile and high-throughput screening of secreted cytokines, chemokines, and growth factors","dates":{"last_updated":"2025-09-24","first_public":"2021-04-16"},"accession":"PRJNA663888","cross_references":{"GEO":["GSE158072"],"taxon":["9606"],"PubMed":["33820914"]}}