<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nam DE</submitter><funding>National Institutes of Health</funding><pagination>e0306345</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11210754</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(6)</volume><pubmed_abstract>Chronic liver diseases are caused by hepatic viral infection, chemicals, and metabolic stress. The protein Grb2-associated binder 1 (Gab1) binds to various growth factor receptors, and triggers cell differentiation/survival signaling pathways. To identify signaling molecules involved in the progression of liver diseases, we performed reverse-phase protein microarray (RPMA)-based screening of hepatocytes isolated from humanized mice after acute HCV infection. Acute viral infection in humanized liver mice significantly decreased the level of hepatocyte p-Gab1. Moreover, hepatoma cells upon HCV infection decreased Gab1 mRNA at later times of infection (D3 to D5) and p-Gab1 level was inversely related to the production of TGF-β. In contrast, the level of p-Gab1 was increased in CCL4-induced fi</pubmed_abstract><journal>PloS one</journal><pubmed_title>Activated Gab1 drives hepatocyte proliferation and anti-apoptosis in liver fibrosis via potential involvement of the HGF/c-Met signaling axis.</pubmed_title><pmcid>PMC11210754</pmcid><funding_grant_id>R42 AI122666-03</funding_grant_id><funding_grant_id>R01 Dk122737</funding_grant_id><pubmed_authors>Hakami RM</pubmed_authors><pubmed_authors>Nam DE</pubmed_authors><pubmed_authors>Um E</pubmed_authors><pubmed_authors>Omole S</pubmed_authors><pubmed_authors>Hahn YS</pubmed_authors><pubmed_authors>Park SJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Activated Gab1 drives hepatocyte proliferation and anti-apoptosis in liver fibrosis via potential involvement of the HGF/c-Met signaling axis.</name><description>Chronic liver diseases are caused by hepatic viral infection, chemicals, and metabolic stress. The protein Grb2-associated binder 1 (Gab1) binds to various growth factor receptors, and triggers cell differentiation/survival signaling pathways. To identify signaling molecules involved in the progression of liver diseases, we performed reverse-phase protein microarray (RPMA)-based screening of hepatocytes isolated from humanized mice after acute HCV infection. Acute viral infection in humanized liver mice significantly decreased the level of hepatocyte p-Gab1. Moreover, hepatoma cells upon HCV infection decreased Gab1 mRNA at later times of infection (D3 to D5) and p-Gab1 level was inversely related to the production of TGF-β. In contrast, the level of p-Gab1 was increased in CCL4-induced fi</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-19T18:35:47.103Z</modification><creation>2025-04-19T18:35:47.103Z</creation></dates><accession>S-EPMC11210754</accession><cross_references><pubmed>38935609</pubmed><doi>10.1371/journal.pone.0306345</doi></cross_references></HashMap>