Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

Dataset Information

0

Human liver biopsy of different phases from control to NASH


ABSTRACT: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder in industrialized countries. Liver samples from morbidly obese patients (N=45) with all stages of NAFLD and controls (N=18) were analysed by array-based DNA methylation and mRNA expression profiling. NAFLD-specific expression and methylation differences were seen for nine genes coding for key enzymes in intermediate metabolism (including PC, ACLY, PLCG1) and insulin/insulin-like signalling (including IGF1, IGFBP2, PRKCE) and replicated by bisulfite pyrosequening (independent N=39). Transcription factor binding sites at NAFLD-specific CpG sites were >1000-fold enriched for ZNF274, PGC1A and SREBP2. Intra-individual comparison of liver biopsies before and after bariatric surgery showed NAFLD-associated methylation changes to be partially reversible. Post-bariatric and NAFLD-specific methylation signatures were clearly distinct both in gene-ontology and transcription factor binding site analyses, with >400-fold enrichment of NRF1, HSF1 and ESRRA sites. Our findings provide one of the first examples of treatment-induced epigenetic organ remodelling in humans. 73 samples of human liver grouped into C (control=14), H (healthy obese=27), S (steatosis=14) and N (nash=18). This dataset is part of the TransQST collection.

ORGANISM(S): Homo sapiens

SUBMITTER: Timo Itzel 

PROVIDER: E-GEOD-48452 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

altmetric image

Publications


Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder in industrialized countries. Liver samples from morbidly obese patients (n = 45) with all stages of NAFLD and controls (n = 18) were analyzed by array-based DNA methylation and mRNA expression profiling. NAFLD-specific expression and methylation differences were seen for nine genes coding for key enzymes in intermediate metabolism (including PC, ACLY, and PLCG1) and insulin/insulin-like signaling (including IGF1,  ...[more]

Similar Datasets

2013-08-08 | GSE48452 | GEO
2017-07-11 | GSE83452 | GEO
2013-08-08 | E-GEOD-48325 | biostudies-arrayexpress
2020-12-07 | GSE155973 | GEO
2015-07-02 | E-GEOD-59045 | biostudies-arrayexpress
2014-09-17 | E-GEOD-61446 | biostudies-arrayexpress
2013-08-08 | GSE48325 | GEO
2018-03-15 | E-MTAB-4856 | biostudies-arrayexpress
2014-09-17 | GSE61446 | GEO
2015-11-01 | E-GEOD-46300 | biostudies-arrayexpress