The flavoprotein FOXRED2 reductively activates nitro-chloromethylbenzindolines and other hypoxia-targeting prodrugs

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dc.contributor.author Hunter, Francis en
dc.contributor.author Jaiswal, Jagdish en
dc.contributor.author Hurley, DG en
dc.contributor.author Liyanage, HDS en
dc.contributor.author McManaway, Sarah en
dc.contributor.author Gu, Yongchuan en
dc.contributor.author Richter, S en
dc.contributor.author Wang, Jingli en
dc.contributor.author Tercel, Moana en
dc.contributor.author Print, Cristin en
dc.contributor.author Wilson, William en
dc.contributor.author Pruijn, Frederik en
dc.date.accessioned 2018-10-15T03:56:21Z en
dc.date.issued 2014-05-15 en
dc.identifier.citation Biochemical Pharmacology, 2014, 89 (2), pp. 224 - 235 en
dc.identifier.issn 0006-2952 en
dc.identifier.uri http://hdl.handle.net/2292/41708 en
dc.description.abstract The nitro-chloromethylbenzindoline prodrug SN29428 has been rationally designed to target tumour hypoxia. SN29428 is metabolised to a DNA minor groove alkylator via oxygen-sensitive reductive activation initiated by unknown one-electron reductases. The present study sought to identify reductases capable of activating SN29428 in tumours. Expression of candidate reductases in cell lines was modulated using forced expression and, for P450 (cytochrome) oxidoreductase (POR), by zinc finger nuclease-mediated gene knockout. Affymetrix microarray mRNA expression of flavoreductases was correlated with SN29428 activation in a panel of 23 cancer cell lines. Reductive activation and cytotoxicity of prodrugs were measured using mass spectrometry and antiproliferative assays, respectively. SN29428 activation under hypoxia was strongly attenuated by the pan-flavoprotein inhibitor diphenyliodonium, but less so by knockout of POR suggesting other flavoreductases contribute. Forced expression of 5-methyltetrahydrofolate-homocysteine methyltransferase reductase (MTRR), as well as POR, increased activation of SN29428 in hypoxic HCT 116 cells. SN29428 activation strongly correlated with expression of POR and also FAD-dependent oxidoreductase domain containing 2 (FOXRED2), in cancer cell lines. This association persisted after removing the effect of POR enzyme activity using first-order partial correlation. Forced expression of FOXRED2 increased SN29428 activation and cytotoxicity in hypoxic HEK293 cells and also increased activation of hypoxia-targeted prodrugs PR-104A, tirapazamine and SN30000, and increased cytotoxicity of the clinical-stage prodrug TH-302. Thus this study has identified three flavoreductases capable of enzymatically activating SN29428, one of which (FOXRED2) has not previously been implicated in xenobiotic metabolism. These results will inform future development of biomarkers predictive of SN29428 sensitivity. en
dc.relation.ispartofseries Biochemical Pharmacology en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/ en
dc.title The flavoprotein FOXRED2 reductively activates nitro-chloromethylbenzindolines and other hypoxia-targeting prodrugs en
dc.type Journal Article en
dc.identifier.doi 10.1016/j.bcp.2014.03.001 en
pubs.issue 2 en
pubs.begin-page 224 en
pubs.volume 89 en
dc.rights.holder Copyright Elsevier en
dc.identifier.pmid 24632291 en
pubs.author-url http://www.sciencedirect.com/science/article/pii/S0006295214001592 en
pubs.end-page 235 en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Article en
pubs.elements-id 429419 en
pubs.org-id Medical and Health Sciences en
pubs.org-id Medical Sciences en
pubs.org-id Auckland Cancer Research en
pubs.org-id Molecular Medicine en
pubs.org-id Science en
pubs.org-id Science Research en
pubs.org-id Maurice Wilkins Centre (2010-2014) en
dc.identifier.eissn 1873-2968 en
pubs.record-created-at-source-date 2014-03-02 en
pubs.dimensions-id 24632291 en


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