Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/136253
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dc.creatorDuarte, D
dc.creatorAmaro, F
dc.creatorSilva, I
dc.creatorSilva, D
dc.creatorFresco, P
dc.creatorOliveira, JC
dc.creatorReguengo, H
dc.creatorGonçalves, J
dc.creatorVale, N
dc.date.accessioned2021-09-20T10:52:24Z-
dc.date.available2021-09-20T10:52:24Z-
dc.date.issued2019
dc.identifier.issn2218-273X
dc.identifier.urihttps://hdl.handle.net/10216/136253-
dc.description.abstractCarbidopa is used for the treatment of Parkinson’s disease (PD) as an inhibitor of DOPA decarboxylase, and PD patients taking carbidopa have a lower incidence of various tumors, except for breast cancer andmelanoma. Recently, itwas shown that carbidopa inhibits tryptophan-2,3-dioxygenase (TDO) and kynureninase enzymes. In the present study, the effect of carbidopa on the viability and metabolic profile of breast cancer MCF-7 and melanoma A375 cells was investigated. Carbidopa was not effective in inhibiting MCF-7 and A375 proliferation. Liquid chromatography and mass spectrometry revealed a new compound, identified as indole-3-acetonitrile (IAN), which promoted a concentration-dependent increase in the viability of both cell lines. The results suggest that treatment with carbidopa may alter tryptophan (Trp) metabolism in breast cancer and melanoma leading to the formation of a pro-proliferative Trp metabolite, which may contribute to its failure in reducing breast cancers and melanoma incidence in PD patients taking carbidopa.
dc.description.sponsorshipThis work was financed by FEDER—Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020—OperationalProgramme for Competitiveness and Internationalisation (POCI), Portugal 2020, and by Portuguese funds through FCT, in the framework of the project “Institute for Research and Innovation in Health Sciences” (POCI-01-0145-FEDER-007274).” NV thanks FCT for IF position, Fundação Manuel António da Mota (FMAM, Portugal) for support. The contents of this report are solely the responsibility of the authors and do not necessarily represent the official views of the FCT and FMAM. This work was financed by Portuguese founds from Fundação para a Ciência e a Tecnologia (FCT), grant number IF/00092/2014/CP1255/CT0004.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofBiomolecules, vol.9(9):409
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectA375 cell line
dc.subjectCarbidopa
dc.subjectIndole-3-acetonitrile
dc.subjectMCF-7 cell line
dc.subjectTryptophan
dc.subject.meshBreast Neoplasms / metabolism
dc.subject.meshBreast Neoplasms / pathology
dc.subject.meshCarbidopa / pharmacology
dc.subject.meshCell Line, Tumor
dc.subject.meshCell Proliferation / drug effects
dc.subject.meshCell Survival / drug effects
dc.subject.meshChromatography, High Pressure Liquid
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshIndoles / analysis
dc.subject.meshIndoles / metabolism
dc.subject.meshMelanoma / metabolism
dc.subject.meshMelanoma / pathology
dc.subject.meshSkin Neoplasms / metabolism
dc.subject.meshSkin Neoplasms / pathology
dc.subject.meshSpectrometry, Mass, Electrospray Ionization
dc.subject.meshTryptophan / metabolism
dc.titleCarbidopa alters tryptophan metabolism in breast cancer and melanoma cells leading to the formation of indole-3-acetonitrile, a pro-proliferative metabolite
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde
dc.identifier.doi10.3390/biom9090409
dc.relation.publisherversionhttps://www.mdpi.com/2218-273X/9/9/409
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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