<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Veronica Busa</submitter><organism>Heterocephalus glaber</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-13538</full_dataset_link><description>Mice are cancer-prone, whereas naked mole-rats are cancer-resistant. Because fibroblasts support the development of skin cancer, SCC25 cells were co-cultured with either mouse or naked-mole rat cells and the difference in SCC25 cells grown alone or with the different types of fibroblasts were compared. Cells were grown together for two days, then FACS-sorted and bulk-sequenced separately.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Pooled libraries were sequenced in one P3 flow cell on a Illumina  Illumina NextSeq2000 sequencer using a 100 bp paired-end read protocol.</sample_protocol><sample_protocol>Library Construction - RNA-sequencing libraries prepared using Illumina stranded total RNA Prep, Ligation with RiboZero Plus (Illimuna) following manufacturer's instructions.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted by adding 800 µl TRIzol reagent (Life Technologies). Total RNA samples were DNased treated using Turbo DNase (Life Technologies).</sample_protocol><sample_protocol>Sample Collection - For two-dimensional co-culture, SCC25-tdTomato cells were seeded in a 1:1 ratio with mouse or naked mole-rat fibroblasts in DMEM/F12 medium (11320-032, Life Technologies) supplemented with 0.05% FBS (Life Technologies), 400 ng/ml hydrocortisone (Santa Cruz Biotechnology) and 1% Penicillin-Streptomycin (PEST) and cultured in a 37°C incubator with 5% CO2. After 48 hours SCC25-tdTomato and fibroblasts were separated using FACS sorting (E-cadherin-APC staining to separate SCC25 from fibroblasts (TdTom &amp;E-cadherin-). Approximately 50,000-100,000 cells were sorted of each cell type from each condition.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Sequence Alignment - Each sample was aligned to its corresponding species' genome (GRCh38, GRCm10, HetGla_female) via STAR 2.7.10a</data_protocol><data_protocol>Data Transformation - Ortholog lists were derived from Ensembl and counts were taken from STAR output. Reads for many-to-one orthologs were summed. Counts were log-transformed and genes with no expression were excluded for downstream analysis.</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>NextSeq 2000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Heterocephalus glaber</species><pubmed_authors>Veronica Busa</pubmed_authors><pubmed_authors>Mikaela Behm</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bulk RNA-seq of co-cultured SCC25 and mouse or naked mole-rat fibroblasts</name><description>Mice are cancer-prone, whereas naked mole-rats are cancer-resistant. Because fibroblasts support the development of skin cancer, SCC25 cells were co-cultured with either mouse or naked-mole rat cells and the difference in SCC25 cells grown alone or with the different types of fibroblasts were compared. Cells were grown together for two days, then FACS-sorted and bulk-sequenced separately.</description><dates><release>2025-12-31T00:00:00Z</release><modification>2025-12-31T02:02:13.217Z</modification><creation>2023-11-16T19:19:39.038Z</creation></dates><accession>E-MTAB-13538</accession><cross_references><ENA>ERP154468</ENA><Biostudies>E-MTAB-12459</Biostudies><Biostudies>E-MTAB-12454</Biostudies><Biostudies>E-MTAB-12456</Biostudies><Biostudies>E-MTAB-12461</Biostudies><Biostudies>E-MTAB-12451</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>