{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Knowles LM"],"funding":["NCRR NIH HHS","NHLBI NIH HHS","NCI NIH HHS"],"pagination":["31378-84"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2581575"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["283(46)"],"pubmed_abstract":["Fatty-acid synthase (FAS) is up-regulated in a broad range of cancers, including those of the breast, prostate, and ovaries. In tumor cells, the inhibition of FAS elicits cell cycle arrest and apoptosis, so it is considered a potential drug target for oncology. Results from this study show that inhibition of FAS, by either knockdown with small interfering RNA or inhibition with the small molecule drug orlistat, leads to activation of the receptor-mediated apoptotic cascade (caspase-8-mediated) and ultimately to cell death. However, knockdown of two enzymes upstream of FAS, acetyl-CoA carboxylase-alpha and ATP-citrate lyase, fails to activate caspase-8 or to elicit apoptosis in tumor cells, even though palmitate synthesis was suppressed. Using differential gene analysis, we traced the uniqu"],"journal":["The Journal of biological chemistry"],"pubmed_title":["Inhibition of fatty-acid synthase induces caspase-8-mediated tumor cell apoptosis by up-regulating DDIT4."],"pmcid":["PMC2581575"],"funding_grant_id":["RR020843","HL080718","CA6982713","CA69306","CA108959"],"pubmed_authors":["Knowles LM","Smith JW","Osterman A","Yang C"],"additional_accession":[]},"is_claimable":false,"name":"Inhibition of fatty-acid synthase induces caspase-8-mediated tumor cell apoptosis by up-regulating DDIT4.","description":"Fatty-acid synthase (FAS) is up-regulated in a broad range of cancers, including those of the breast, prostate, and ovaries. In tumor cells, the inhibition of FAS elicits cell cycle arrest and apoptosis, so it is considered a potential drug target for oncology. Results from this study show that inhibition of FAS, by either knockdown with small interfering RNA or inhibition with the small molecule drug orlistat, leads to activation of the receptor-mediated apoptotic cascade (caspase-8-mediated) and ultimately to cell death. However, knockdown of two enzymes upstream of FAS, acetyl-CoA carboxylase-alpha and ATP-citrate lyase, fails to activate caspase-8 or to elicit apoptosis in tumor cells, even though palmitate synthesis was suppressed. Using differential gene analysis, we traced the uniqu","dates":{"release":"2008-01-01T00:00:00Z","publication":"2008 Nov","modification":"2026-03-16T16:39:02.888Z","creation":"2019-03-27T00:19:17Z"},"accession":"S-EPMC2581575","cross_references":{"pubmed":["18796435"],"doi":["10.1074/jbc.m803384200","10.1074/jbc.M803384200"]}}