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dc.rights.licenseopenen_US
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorSEREN, Seda
dc.contributor.authorJOLY, Jean-Patrick
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorVOISIN, Pierre
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorBOUCHAUD, Véronique
dc.contributor.authorAUDRAN, Gérard
dc.contributor.authorMARQUE, Sylvain R A
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorMELLET, Philippe
dc.date.accessioned2022-11-30T15:56:29Z
dc.date.available2022-11-30T15:56:29Z
dc.date.issued2022-07-14
dc.identifier.issn1520-4804en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170440
dc.description.abstractEnCurrent chemotherapies suffer low specificity and sometimes drug resistance. Neutrophil elastase activity in cancer is associated with poor prognosis and metastasis settlement. More generally, tumors harbor various and persistent protease activities unseen in healthy tissues. In an attempt to be more specific, we designed prodrugs that are activatable by neutrophil elastase. Upon activation, these alkoxyamine-based drugs release cytotoxic alkyl radicals that act randomly to prevent drug resistance. As a result, U87 glioblastoma cells displayed high level caspase 3/7 activation during the first hour of exposure in the presence of human neutrophil elastase and the prodrug in vitro. The apoptosis process and cell death occurred between 24 and 48 h after exposure with a half lethal concentration of 150 μM. These prodrugs are versatile and easy to synthetize and can be adapted to many enzymes.
dc.language.isoENen_US
dc.subject.enAntineoplastic Agents
dc.subject.enGlioblastoma
dc.subject.enHumans
dc.subject.enLeukocyte Elastase
dc.subject.enNeutrophils
dc.subject.enProdrugs
dc.title.enNeutrophil Elastase-Activatable Prodrugs Based on an Alkoxyamine Platform to Deliver Alkyl Radicals Cytotoxic to Tumor Cells.
dc.title.alternativeJ Med Chemen_US
dc.typeArticle de revueen_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed35764297en_US
bordeaux.journalJournal of Medicinal Chemistryen_US
bordeaux.page9253-9266en_US
bordeaux.volume65en_US
bordeaux.hal.laboratoriesCentre de Résonance Magnétique des Systèmes Biologiques (CRMSB) - UMR 5536en_US
bordeaux.issue13en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03879852
hal.version1
hal.date.transferred2022-11-30T15:56:32Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Medicinal%20Chemistry&rft.date=2022-07-14&rft.volume=65&rft.issue=13&rft.spage=9253-9266&rft.epage=9253-9266&rft.eissn=1520-4804&rft.issn=1520-4804&rft.au=SEREN,%20Seda&JOLY,%20Jean-Patrick&VOISIN,%20Pierre&BOUCHAUD,%20V%C3%A9ronique&AUDRAN,%20G%C3%A9rard&rft.genre=article


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