{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10"],"submitter":["Meier-Menches SM"],"pubmed_abstract":["Acute promyelocytic leukaemia (APL) can be cured by the co-administration of arsenic trioxide (ATO) and all-<i>trans</i> retinoic acid (ATRA). These small molecules relieve the differentiation blockade of the transformed promyelocytes and trigger their maturation into functional neutrophils, which are physiologically primed for apoptosis. This normalization therapy represents a compelling alternative to cytotoxic anticancer chemotherapy, but lacks an <i>in vitro</i> model system for testing the efficiency of novel combination treatments consisting of inducers of differentiation and metallopharmaceuticals. Here, using proteome profiling we present an experimental framework that enables characterising the differentiation- and metal-specific effects of the combination treatment in a panel of "],"journal":["Frontiers in chemistry"],"pagination":["826346"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8844467"],"repository":["biostudies-literature"],"pubmed_title":["A Proteomic Platform Enables to Test for AML Normalization <i>In Vitro</i>."],"pmcid":["PMC8844467"],"pubmed_authors":["Gerner C","Meier-Menches SM","Janker L","Schmetterer KG","Neuditschko B","Reichle A","Gerner MC"],"additional_accession":[]},"is_claimable":false,"name":"A Proteomic Platform Enables to Test for AML Normalization <i>In Vitro</i>.","description":"Acute promyelocytic leukaemia (APL) can be cured by the co-administration of arsenic trioxide (ATO) and all-<i>trans</i> retinoic acid (ATRA). These small molecules relieve the differentiation blockade of the transformed promyelocytes and trigger their maturation into functional neutrophils, which are physiologically primed for apoptosis. This normalization therapy represents a compelling alternative to cytotoxic anticancer chemotherapy, but lacks an <i>in vitro</i> model system for testing the efficiency of novel combination treatments consisting of inducers of differentiation and metallopharmaceuticals. Here, using proteome profiling we present an experimental framework that enables characterising the differentiation- and metal-specific effects of the combination treatment in a panel of ","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-04-18T16:34:44.03Z","creation":"2025-04-07T03:52:25.23Z"},"accession":"S-EPMC8844467","cross_references":{"pubmed":["35178376"],"doi":["10.3389/fchem.2022.826346"]}}