Data on novel DNA methylation changes induced by valproic acid in human hepatocytes
| Autor: | Jarno E J Wolters, SandraM Claessen, JosCS Kleinjans, TheoMCM de Kok, SimoneGJ van Breda |
|---|---|
| Přispěvatelé: | RS: GROW - R1 - Prevention, Promovendi ODB, Toxicogenomics, RS: FHML MaCSBio, RS: FPN MaCSBio, RS: FSE MaCSBio |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Steatosis Valproic acid (VPA) Primary human hepatocytes (PHHs) Pharmacology Biology lcsh:Computer applications to medicine. Medical informatics 03 medical and health sciences chemistry.chemical_compound medicine lcsh:Science (General) EP300 Cytotoxicity Gene Genetics Genomics and Molecular Biology Valproic Acid DNA methylation Multidisciplinary Methylated DNA Immuno-Precipitation-sequencing (MeDIP-seq) Methylation MEDIP-SEQ medicine.disease 030104 developmental biology chemistry Biochemistry lcsh:R858-859.7 lipids (amino acids peptides and proteins) DNA lcsh:Q1-390 medicine.drug |
| Zdroj: | Data in brief, 16, 161-171. Elsevier Science Data in Brief, Vol 16, Iss, Pp 161-171 (2018) Data in Brief |
| ISSN: | 2352-3409 |
| DOI: | 10.1016/j.dib.2017.11.031 |
| Popis: | Valproic acid (VPA) is a widely prescribed antiepileptic drug in the world. Despite its pharmacological importance, it may cause liver toxicity and steatosis. However the exact mechanism of the steatosis formation is unknown. The data presented in this DIB publication is used to further investigate the VPA-induced mechanisms of steatosis by analyzing changes in patterns of methylation. Therefore, primary human hepatocytes (PHHs) were exposed to VPA at a concentration which was shown to cause steatosis without inducing overt cytotoxicity. VPA was administered for 5 days daily to PHHs. Furthermore, after 5 days VPA-treatment parts of the PHHs were followed for a 3 days washout. Differentially methylated DNA regions (DMRs) were identified by using the ‘Methylated DNA Immuno-Precipitation - sequencing’ (MeDIP-seq) method. The data presented in this DIB demonstrate induced steatosis pathways by all DMRs during VPA-treatment, covering interesting drug-induced steatosis genes (persistent DMRs upon terminating VPA treatment and the EP300 network). This was illustrated in our associated article (Wolters et al., 2017) [1]. MeDIP-seq raw data are available on ArrayExpress (accession number: E-MTAB-4437). Keywords: DNA methylation, Methylated DNA Immuno-Precipitation-sequencing (MeDIP-seq), Primary human hepatocytes (PHHs), Steatosis, Valproic acid (VPA) |
| Databáze: | OpenAIRE |
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