<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Massey V</submitter><funding>NIDDK NIH HHS</funding><funding>Medical Research Council</funding><funding>NIAAA NIH HHS</funding><pagination>1725-1740.e2</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8613537</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>160(5)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>We recently showed that alcoholic hepatitis (AH) is characterized by dedifferentiation of hepatocytes and loss of mature functions. Glucose metabolism is tightly regulated in healthy hepatocytes. We hypothesize that AH may lead to metabolic reprogramming of the liver, including dysregulation of glucose metabolism.&lt;h4>Methods&lt;/h4>We performed integrated metabolomic and transcriptomic analyses of liver tissue from patients with AH or alcoholic cirrhosis or normal liver tissue from hepatic resection. Focused analyses of chromatin immunoprecipitation coupled to DNA sequencing was performed. Functional in vitro studies were performed in primary rat and human hepatocytes and HepG2 cells.&lt;h4>Results&lt;/h4>Patients with AH exhibited specific changes in the levels of interme</pubmed_abstract><journal>Gastroenterology</journal><pubmed_title>Integrated Multiomics Reveals Glucose Use Reprogramming and Identifies a Novel Hexokinase in Alcoholic Hepatitis.</pubmed_title><pmcid>PMC8613537</pmcid><funding_grant_id>P30 DK120531</funding_grant_id><funding_grant_id>R24 AA025017</funding_grant_id><funding_grant_id>R01 AA018873</funding_grant_id><funding_grant_id>F31 AA024969</funding_grant_id><funding_grant_id>U01 AA026972</funding_grant_id><funding_grant_id>MR/R023026/1</funding_grant_id><funding_grant_id>U01 AA021908</funding_grant_id><funding_grant_id>R01 DK110355</funding_grant_id><funding_grant_id>U01 AA026264</funding_grant_id><funding_grant_id>P50 AA027054</funding_grant_id><funding_grant_id>U01 AA026978</funding_grant_id><funding_grant_id>T32 AA007463</funding_grant_id><pubmed_authors>Morales-Arraez D</pubmed_authors><pubmed_authors>Altamirano J</pubmed_authors><pubmed_authors>Massey V</pubmed_authors><pubmed_authors>Cameron A</pubmed_authors><pubmed_authors>Argemi J</pubmed_authors><pubmed_authors>Caballeria J</pubmed_authors><pubmed_authors>Vadigepalli R</pubmed_authors><pubmed_authors>Dubuquoy L</pubmed_authors><pubmed_authors>Louvet A</pubmed_authors><pubmed_authors>Odena G</pubmed_authors><pubmed_authors>Shah V</pubmed_authors><pubmed_authors>Villanueva C</pubmed_authors><pubmed_authors>Millan C</pubmed_authors><pubmed_authors>Mello A</pubmed_authors><pubmed_authors>Bataller R</pubmed_authors><pubmed_authors>Garcia-Rocha M</pubmed_authors><pubmed_authors>Sancho-Bru P</pubmed_authors><pubmed_authors>Parrish A</pubmed_authors><pubmed_authors>Sun Z</pubmed_authors><pubmed_authors>Mathurin P</pubmed_authors><pubmed_authors>Adrover A</pubmed_authors><pubmed_authors>Morgan TR</pubmed_authors><pubmed_authors>Mann J</pubmed_authors><pubmed_authors>Alvarado-Tapias E</pubmed_authors><pubmed_authors>Morales-Ibanez O</pubmed_authors><pubmed_authors>Affo S</pubmed_authors><pubmed_authors>Cao S</pubmed_authors><pubmed_authors>Moreno M</pubmed_authors><pubmed_authors>Martinez C</pubmed_authors><pubmed_authors>Snider N</pubmed_authors><pubmed_authors>Guinovart J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integrated Multiomics Reveals Glucose Use Reprogramming and Identifies a Novel Hexokinase in Alcoholic Hepatitis.</name><description>&lt;h4>Background &amp; aims&lt;/h4>We recently showed that alcoholic hepatitis (AH) is characterized by dedifferentiation of hepatocytes and loss of mature functions. Glucose metabolism is tightly regulated in healthy hepatocytes. We hypothesize that AH may lead to metabolic reprogramming of the liver, including dysregulation of glucose metabolism.&lt;h4>Methods&lt;/h4>We performed integrated metabolomic and transcriptomic analyses of liver tissue from patients with AH or alcoholic cirrhosis or normal liver tissue from hepatic resection. Focused analyses of chromatin immunoprecipitation coupled to DNA sequencing was performed. Functional in vitro studies were performed in primary rat and human hepatocytes and HepG2 cells.&lt;h4>Results&lt;/h4>Patients with AH exhibited specific changes in the levels of interme</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-05-09T04:12:58.096Z</modification><creation>2025-02-18T23:36:04.246Z</creation></dates><accession>S-EPMC8613537</accession><cross_references><pubmed>33309778</pubmed><doi>10.1053/j.gastro.2020.12.008</doi></cross_references></HashMap>