(−)-UB006: A new fatty acid synthase inhibitor and cytotoxic agent without anorexic side effects

dc.contributor.authorMakowski, Kamil
dc.contributor.authorMir Bonnín, Joan Francesc
dc.contributor.authorMera Nanín, Paula
dc.contributor.authorAriza Piquer, Xavier
dc.contributor.authorAsins Muñoz, Guillermina
dc.contributor.authorHegardt, Fausto
dc.contributor.authorHerrero Rodríguez, Laura
dc.contributor.authorGarcía Gómez, Jordi
dc.contributor.authorSerra i Cucurull, Dolors
dc.date.accessioned2017-03-29T16:45:45Z
dc.date.available2017-03-29T16:45:45Z
dc.date.issued2017-03-12
dc.date.updated2017-03-29T16:45:45Z
dc.description.abstractC75 is a synthetic anticancer drug that inhibits fatty acid synthase (FAS) and shows a potent anorexigenic side effect. In order to find new cytotoxic compounds that do not impact food intake, we synthesized a new family of C75 derivatives. The most promising anticancer compound among them was UB006 ((4SR,5SR)-4-(hydroxymethyl)-3-methylene-5-octyldihydrofuran-2(3H)-one). The effects of this compound on cytotoxicity, food intake and body weight were studied in UB006 racemic mixture and in both its enantiomers separately. The results showed that both enantiomers inhibit FAS activity and have potent cytotoxic effects in several tumour cell lines, such as the ovarian cell cancer line OVCAR-3. The (−)-UB006 enantiomer's cytotoxic effect on OVCAR-3 was 40-fold higher than that of racemic C75, and 2- and 38-fold higher than that of the racemic mixture and its opposite enantiomer, respectively. This cytotoxic effect on the OVCAR-3 cell line involves mechanisms that reduce mitochondrial respiratory capacity and ATP production, DDIT4/REDD1 upregulation, mTOR activity inhibition, and caspase-3 activation, resulting in apoptosis. In addition, central and peripheral administration of (+)-UB006 or (−)-UB006 into rats and mice did not affect food intake or body weight. Altogether, our data support the discovery of a new potential anticancer compound (−)-UB006 that has no anorexigenic side effects.
dc.format.extent15 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec670544
dc.identifier.issn0223-5234
dc.identifier.pmid28324785
dc.identifier.urihttps://hdl.handle.net/2445/109130
dc.language.isoeng
dc.publisherElsevier Masson SAS
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.ejmech.2017.03.012
dc.relation.ispartofEuropean Journal of Medicinal Chemistry, 2017, vol. 131, p. 207-221
dc.relation.urihttps://doi.org/10.1016/j.ejmech.2017.03.012
dc.rights(c) Elsevier Masson SAS, 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Química Inorgànica i Orgànica)
dc.subject.classificationÀcids grassos
dc.subject.classificationInhibidors enzimàtics
dc.subject.classificationCàncer d'ovari
dc.subject.classificationEnantiòmers
dc.subject.otherFatty acids
dc.subject.otherEnzyme inhibitors
dc.subject.otherOvarian cancer
dc.subject.otherEnantiomers
dc.title(−)-UB006: A new fatty acid synthase inhibitor and cytotoxic agent without anorexic side effects
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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