<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Carl MANN</submitter><organism>Homo sapiens</organism><software>Salmon and tximeta</software><software>EdgeR and Limma</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16030</full_dataset_link><description>Transcriptomic analysis of inflammatory gene expression in a human mammary fibroblast cell line in proliferation and IR-induced senescence, with and without IL1-alpha treatment (10 pg/ml for 24 hours). Cells were induced into senescence by irradiation with 40 Gy of 120 kV X-rays and then incubated 9 days before treating with IL1-alpha.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Paired-End 42 nucleotides in an Illumina NextSeq 500 sequencer.</sample_protocol><sample_protocol>Growth Protocol - DMEM + glutamine + pyruvate + pen/strep in 5% O2 + 5% CO2 incubator.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was extracted with the Macherey-Nagel Nucleospin RNA Plus.</sample_protocol><sample_protocol>Sample Collection - Cell monolayers were trypsinized, neutralized with medium, washed with PBS, and centrifuged. Washed cell pellets were resuspended in Macherey-Nagel Nucleospin RNA Plus Lysis Buffer.</sample_protocol><sample_protocol>Library Construction - NEBNext Ultra II Directional RNA Library Kit with PolyA RNA selection</sample_protocol><sample_protocol>Sample Treatment - Proliferating cells were treated with 10 pg/ml Interleukin-alpha (Sigma I2778)for 24 hours. M168 cells were induced into senescence by irradiating with 40 Gy of 120 KV X-rays produced by a Faxitron 43855D generator. Cells were incubated for 10 days post irradiation before harvesting for RNA isolation. For IL1-alpha treatment of irradiated cells, the cells were irradiated with 40 Gy of 120 KV X-rays as above and cells were incubated for 9 days and then treated for 24 hours with 10 pg/ml of IL1-alpha (Sigma I2778).</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Data were normalized with EdgeR and Limma voom</data_protocol><data_protocol>Sequence Alignment - Fastq sequences were mappled to the human transcriptome using the Salmon transcriptome alignment software.</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>NextSeq 550</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><pubmed_authors>Carl MANN</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of a human mammary fibroblast cell line in proliferation and IR-induced senescence with and without IL1-alpha treatment.</name><description>Transcriptomic analysis of inflammatory gene expression in a human mammary fibroblast cell line in proliferation and IR-induced senescence, with and without IL1-alpha treatment (10 pg/ml for 24 hours). Cells were induced into senescence by irradiation with 40 Gy of 120 kV X-rays and then incubated 9 days before treating with IL1-alpha.</description><dates><release>2026-01-01T00:00:00Z</release><modification>2026-01-02T02:03:17.382Z</modification><creation>2025-11-06T12:48:18.069Z</creation></dates><accession>E-MTAB-16030</accession><cross_references><ENA>ERP183775</ENA><Biostudies>E-MTAB-14265</Biostudies><Biostudies>E-MTAB-14201</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>