{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["19(3)"],"submitter":["Liu Z"],"pubmed_abstract":["Alcohol-related liver disease (ALD) is the most common chronic liver disease worldwide; however, no effective treatment to prevent the progression of alcohol-related liver fibrosis (ALF) is available. CD73/NT5E, a nucleotidase, controls cellular homeostasis by combining extracellular purinergic signaling with intracellular kinase activity and gene transcription and is associated with cell proliferation, differentiation, and death. In this study, we demonstrated that CD73/NT5E had a more significant regulatory effect on the activation, proliferation, and apoptosis of HSCs compared with that of CD39/ENTPD1. We examined the expression of CD73/NT5E in the normal and fibrotic human livers. The absence of CD73/NT5E was protective in mouse models of ALF. In addition, Kyoto Encyclopedia of Genes a"],"journal":["International journal of biological sciences"],"pagination":["950-966"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9909992"],"repository":["biostudies-literature"],"pubmed_title":["CD73/NT5E-mediated ubiquitination of AURKA regulates alcohol-related liver fibrosis via modulating hepatic stellate cell senescence."],"pmcid":["PMC9909992"],"pubmed_authors":["Sheng X","Lv X","Cai J","Wu B","Zhu H","Zhang M","Xu J","Liu X","Liu Z","Xu T","Du J","Xia G","Wu X"],"additional_accession":[]},"is_claimable":false,"name":"CD73/NT5E-mediated ubiquitination of AURKA regulates alcohol-related liver fibrosis via modulating hepatic stellate cell senescence.","description":"Alcohol-related liver disease (ALD) is the most common chronic liver disease worldwide; however, no effective treatment to prevent the progression of alcohol-related liver fibrosis (ALF) is available. CD73/NT5E, a nucleotidase, controls cellular homeostasis by combining extracellular purinergic signaling with intracellular kinase activity and gene transcription and is associated with cell proliferation, differentiation, and death. In this study, we demonstrated that CD73/NT5E had a more significant regulatory effect on the activation, proliferation, and apoptosis of HSCs compared with that of CD39/ENTPD1. We examined the expression of CD73/NT5E in the normal and fibrotic human livers. The absence of CD73/NT5E was protective in mouse models of ALF. In addition, Kyoto Encyclopedia of Genes a","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023","modification":"2025-05-29T21:48:01.493Z","creation":"2025-05-29T21:48:01.493Z"},"accession":"S-EPMC9909992","cross_references":{"pubmed":["36778123"],"doi":["10.7150/ijbs.80461"]}}