TY - JOUR T1 - Inhibition of the polyamine synthesis enzyme ornithine decarboxylase sensitizes triple-negative breast cancer cells to cytotoxic chemotherapy JF - bioRxiv DO - 10.1101/2020.01.08.899492 SP - 2020.01.08.899492 AU - Renee C. Geck AU - Jackson R. Foley AU - Tracy R. Murray Stewart AU - John M. Asara AU - Robert A. Casero, Jr. AU - Alex Toker Y1 - 2020/01/01 UR - http://biorxiv.org/content/early/2020/01/09/2020.01.08.899492.abstract N2 - Treatment of triple-negative breast cancer (TNBC) is limited by a lack of effective molecular targeted therapies. Recent studies have identified metabolic alterations in cancer cells that can be targeted to improve responses to standard-of-care chemotherapy regimens. We found that exposure of TNBC cells to cytotoxic chemotherapy drugs leads to alterations in arginine and polyamine metabolites due to a reduction in the levels and activity of a rate-limiting polyamine biosynthetic enzyme ornithine decarboxylase (ODC). The reduction in ODC was mediated by its negative regulator, antizyme, targeting ODC to the proteasome for degradation. Treatment with the ODC inhibitor DFMO sensitized TNBC cells to chemotherapy, but this was not observed in receptor-positive breast cancer cells. Moreover, TNBC cell lines showed greater sensitivity to single-agent DFMO, and ODC levels were elevated in TNBC patient samples. Alterations in polyamine metabolism in response to chemotherapy, as well as preferential sensitization of TNBC cells to chemotherapy by DFMO, suggest that ODC may be a targetable metabolic vulnerability in TNBC.ARG2Arginase 2ASS1Argininosuccinate SynthaseAZIantizyme inhibitor (protein)AZINantizyme inhibitor (gene/transcript)CDDPcisplatinDFMOα-difluoromethylornithineDOXOdoxorubicinNOHANω-hydroxy-nor-arginineOAZ1antizyme 1 (gene/transcript)ODCOrnithine DecarboxylasePBTpolyamine blocking therapySAMS-adenosyl methionineArgL-arginineOrnornithinePutputrescineSAMS-adenosyl-L-methionineSpmspermineSpdspermidineTNBCtriple-negative breast cancer ER -