{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Yang B"],"funding":["U.S. Department of Health & Human Services | National Institutes of Health (NIH)"],"pagination":["8388"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11436801"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(1)"],"pubmed_abstract":["Methionine adenosyltransferase 2 A (MAT2A) and MAT2B are essential for hepatic stellate cells (HSCs) activation. Forkhead box M1 (FOXM1) transgenic mice develop liver inflammation and fibrosis. Here we examine if they crosstalk in male mice. We found FOXM1/MAT2A/2B are upregulated after bile duct ligation (BDL) and carbon tetrachloride (CCl<sub>4</sub>) treatment in hepatocytes, HSCs and Kupffer cells (KCs). FDI-6, a FOXM1 inhibitor, attenuates the development and reverses the progression of CCl<sub>4</sub>-induced fibrosis while lowering the expression of FOXM1/MAT2A/2B, which exert reciprocal positive regulation on each other transcriptionally. Knocking down any of them lowers HSCs and KCs activation. Deletion of FOXM1 in hepatocytes, HSCs, and KCs protects from BDL-mediated inflammation"],"journal":["Nature communications"],"pubmed_title":["The role of forkhead box M1-methionine adenosyltransferase 2 A/2B axis in liver inflammation and fibrosis."],"pmcid":["PMC11436801"],"funding_grant_id":["P01CA233452"],"pubmed_authors":["Yang H","Fan W","Lu SC","Zhang J","Mavila N","Cao D","Barbier-Torres L","Yang B","Xiong T","Tsuchiya T","Kalinichenko VV","Chhimwal J","Liu T","Wang J","Ramani K","Mato JM","Peng H","Yang X","Lu L","Tomasi ML","Sinha S","Seki E","Han J"],"additional_accession":[]},"is_claimable":false,"name":"The role of forkhead box M1-methionine adenosyltransferase 2 A/2B axis in liver inflammation and fibrosis.","description":"Methionine adenosyltransferase 2 A (MAT2A) and MAT2B are essential for hepatic stellate cells (HSCs) activation. Forkhead box M1 (FOXM1) transgenic mice develop liver inflammation and fibrosis. Here we examine if they crosstalk in male mice. We found FOXM1/MAT2A/2B are upregulated after bile duct ligation (BDL) and carbon tetrachloride (CCl<sub>4</sub>) treatment in hepatocytes, HSCs and Kupffer cells (KCs). FDI-6, a FOXM1 inhibitor, attenuates the development and reverses the progression of CCl<sub>4</sub>-induced fibrosis while lowering the expression of FOXM1/MAT2A/2B, which exert reciprocal positive regulation on each other transcriptionally. Knocking down any of them lowers HSCs and KCs activation. Deletion of FOXM1 in hepatocytes, HSCs, and KCs protects from BDL-mediated inflammation","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Sep","modification":"2025-04-04T01:54:47.728Z","creation":"2025-04-04T01:54:47.728Z"},"accession":"S-EPMC11436801","cross_references":{"pubmed":["39333125"],"doi":["10.1038/s41467-024-52527-8"]}}