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dc.contributor.authorAvecilla, Fernando
dc.contributor.authorPilon, Adhan
dc.contributor.authorRácz, Bálint
dc.contributor.authorGátszegi, Gerda T.
dc.contributor.authorSpengler, Gabriella
dc.contributor.authorRobalo, M. Paula
dc.contributor.authorEnyedy, Éva Anna
dc.contributor.authorGarcia, Maria Helena
dc.contributor.authorValente, Andreia
dc.date.accessioned2024-09-04T15:14:51Z
dc.date.available2024-09-04T15:14:51Z
dc.date.issued2023
dc.identifier.citationPilon, A., Avecilla, F., Rácz, B., Gátszegi, G. T., Spengler, G., Robalo, M. P., Enyedy, É. A., Garcia, M. H., & Valente, A. (2023). Iron(II)-cyclopentadienyl compounds are cytotoxic against colon adenocarcinoma cell lines: Ethylenebis(diphenylphosphane) vs. triphenylphosphane. Journal of Inorganic Biochemistry, 249. https://doi.org/10.1016/J.JINORGBIO.2023.112386es_ES
dc.identifier.urihttp://hdl.handle.net/2183/38859
dc.description.abstract[Abstract] Structure-activity studies aiming to understand the role of each coligand in the formulation of new metallodrugs is an important subject. In that frame, six new compounds with general formula [Fe(η5-C5H5)(dppe)(L)][CF3SO3] with L = benzonitriles (1–4) or carbon monoxide (5) and compound [Fe(η5-C5H5)(CO)(PPh3)2][CF3SO3] (6) were synthesized and compared with three other previously reported compounds [Fe(η5-C5H5)(CO)(L)(PPh3)][CF3SO3]. We were particularly interested in assessing the effect of dppe vs. (PPh3 + CO) for this set of compounds. For that, all compounds were tested against two human colon adenocarcinoma cell lines, Colo205 and the refractile Colo320 (expressing ABCB1, an efflux pump causing multidrug resistance), showing IC50 values in the micromolar range. The presence of dppe in the compound's coordination sphere over (PPh3 + CO) allows for more redox stable compounds showing higher cytotoxicity and selectivity, with improved cytotoxicity towards resistant cells that is not related to the inhibition of ABCB1. Further studies with GSH and H2O2 for selected compounds indicated that their antioxidant ability is not probably the main responsible for their cytotoxicity.es_ES
dc.description.sponsorshipThis work was funded by Fundação para a Ciência e a Tecnologia (FCT), I.P./MCTES through national funds (PIDDAC) - UIDB/00100/2020, UIDP/00100/2020 and LA/P/0056/2020. Andreia Valente acknowledges CEECIND 2017 (CEECIND/01974/2017; acknowledging FCT, as well as POPH and FSE—European Social Fund). A. P. thank FCT for his Ph.D. Grant (SFRH/BD/139412/2018 and COVID/BD/153267/2023). B.R. was supported by the Szeged Foundation for Cancer Research (Szegedi Rákkutatásért Alapítvány). G.S. was supported by the János Bolyai Research Scholarship (BO/00158/22/5) of the Hungarian Academy of Sciences and by the ÚNKP-22-5-SZTE-588 New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund.es_ES
dc.description.sponsorshipPortugal. Fundação para a Ciência e a Tecnologia; UIDB/00100/2020es_ES
dc.description.sponsorshipPortugal. Fundação para a Ciência e a Tecnologia; UIDP/00100/2020es_ES
dc.description.sponsorshipPortugal. Fundação para a Ciência e a Tecnologia; LA/P/0056/2020es_ES
dc.description.sponsorshipMagyarország. Kulturális és Innovációs Minisztérium; ÚNKP-22-5-SZTE-588es_ES
dc.description.sponsorshipMagyarország. Magyar Tudományos Akadémia; BO/00158/22/5es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.urihttps://doi.org/10.1016/j.jinorgbio.2023.112386es_ES
dc.rightsCC BY-NC-ND 4.0 Attribution-NonCommercial-NoDerivatives 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectIron(II)-cyclopentadienyles_ES
dc.subjectMetallodrugses_ES
dc.subjectAnticanceres_ES
dc.subjectABCB1es_ES
dc.subjectColon adenocarcinomaes_ES
dc.subjectRedox activityes_ES
dc.titleIron(II)-cyclopentadienyl compounds are cytotoxic against colon adenocarcinoma cell lines: Ethylenebis(diphenylphosphane) vs. triphenylphosphanees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleJournal of Inorganic Biochemistryes_ES
UDC.volume249es_ES
UDC.startPageArticle 112386es_ES
dc.identifier.doi0.1016/J.JINORGBIO.2023.112386


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