<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter/><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-15132</full_dataset_link><description>This study investigates the preclinical effects of Tumor Treating Fields (TTFields) in pancreatic ductal adenocarcinoma (PDAC).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - For cDNA libraries preparation, the polyA fraction (mRNA) was purified, followed by fragmentation and generation of double-stranded cDNA. Agencourt AMPure XP beads (Beckman Coulter) were used for cleanup, followed by end repair, UMIs addition, adapter ligation and PCR amplification steps.</sample_protocol><sample_protocol>Sample Collection - Samples were fresh frozen in TRIzol</sample_protocol><sample_protocol>Sample Treatment - TTFields were applied to cells using the inovitroTM system as previously described (Kirson, E.D., et al., Disruption of cancer cell replication by alternating electric fields. Cancer Res, 2004. 64(9): p. 3288-95.) With frequency of 150 kHz and intensity of 1.7 V/cm RMS for 24 and 48 hours.</sample_protocol><sample_protocol>Nucleic Acid Extraction - RNA was purified with TRI reagent as previously described [ Rio, D.C., et al., Purification of RNA Using TRIzol (TRI Reagent). Cold Spring Harbor Protocols, 2010. 2010(6): p. pdb.prot5439. ]</sample_protocol><sample_protocol>Growth Protocol - Grown in a 37 °C humidified incubator in RPMI1640 media supplemented with 10% FBS. All media were further supplemented with 2 mM L-glutamine and 50 μg/ml penicillin/streptomycin.</sample_protocol><sample_protocol>Sequencing - Sequencing was done on Illumina NovoSeq 6000 system.</sample_protocol><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>organisation</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><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>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of coding RNA</study_type><species>Homo sapiens</species><additional_accession>ERP172427</additional_accession><pubmed_authors>Kerem Wainer Katsir</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-seq of pancreatic cell lines AsPC1 and BxPC3 treated with Tumor Treating Fields (TTFields) compared to control samples</name><description>This study investigates the preclinical effects of Tumor Treating Fields (TTFields) in pancreatic ductal adenocarcinoma (PDAC).</description><dates><release>2025-12-30T00:00:00Z</release><modification>2025-12-30T02:02:11.666Z</modification><creation>2025-05-08T14:35:39.958Z</creation></dates><accession>E-MTAB-15132</accession><cross_references><ENA>ERP172427</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003738</EFO><EFO>EFO_0004184</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>