{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Chi Y"],"funding":["Natural Science Foundation of Beijing Municipality","National Natural Science Foundation of China"],"pagination":["1746-1758"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6378191"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["23(3)"],"pubmed_abstract":["FAM3B, also known as PANcreatic DERived factor (PANDER), promotes gluconeogenesis and lipogenesis in hepatocytes. However, the underlying mechanism(s) still remains largely unclear. This study determined the mechanism of PANDER-induced FOXO1 activation in hepatocytes. In mouse livers and cultured hepatocytes, PANDER protein is located in both the cytoplasm and nucleus. Nuclear PANDER distribution was increased in the livers of obese mice. In cultured mouse and human hepatocytes, PANDER was co-localized with FOXO1 in the nucleus. PANDER directly interacted with FOXO1 in mouse and human hepatocytes. PANDER overexpression enhanced PANDER-FOXO1 interaction, and detained FOXO1 in the nucleus upon insulin stimulation in hepatocytes. With the increase in PANDER-FOXO1 interaction, PANDER overexpre"],"journal":["Journal of cellular and molecular medicine"],"pubmed_title":["FAM3B (PANDER) functions as a co-activator of FOXO1 to promote gluconeogenesis in hepatocytes."],"pmcid":["PMC6378191"],"funding_grant_id":["7171006","81471035","81670748","81670787"],"pubmed_authors":["Zhang W","Yang W","Wu Z","Yang J","Geng B","Wang D","Tie L","Chi Y","Meng Y","Wang J","Gao F","Li M"],"additional_accession":[]},"is_claimable":false,"name":"FAM3B (PANDER) functions as a co-activator of FOXO1 to promote gluconeogenesis in hepatocytes.","description":"FAM3B, also known as PANcreatic DERived factor (PANDER), promotes gluconeogenesis and lipogenesis in hepatocytes. However, the underlying mechanism(s) still remains largely unclear. This study determined the mechanism of PANDER-induced FOXO1 activation in hepatocytes. In mouse livers and cultured hepatocytes, PANDER protein is located in both the cytoplasm and nucleus. Nuclear PANDER distribution was increased in the livers of obese mice. In cultured mouse and human hepatocytes, PANDER was co-localized with FOXO1 in the nucleus. PANDER directly interacted with FOXO1 in mouse and human hepatocytes. PANDER overexpression enhanced PANDER-FOXO1 interaction, and detained FOXO1 in the nucleus upon insulin stimulation in hepatocytes. With the increase in PANDER-FOXO1 interaction, PANDER overexpre","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Mar","modification":"2026-07-16T19:39:38.786Z","creation":"2019-08-04T07:57:15Z"},"accession":"S-EPMC6378191","cross_references":{"pubmed":["30488666"],"doi":["10.1111/jcmm.14073"]}}