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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69436
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dc.contributor.authorJasiulionis, Miriam G.-
dc.contributor.authorLuchessi, Augusto D.-
dc.contributor.authorMoreira, Andreia G.-
dc.contributor.authorSouza, Pedro P. C.-
dc.contributor.authorSuenaga, Ana P. M.-
dc.contributor.authorCorrea, Mariangela-
dc.contributor.authorCosta, Carlos A. S.-
dc.contributor.authorCuri, Rui-
dc.contributor.authorCosta-Neto, Claudio M.-
dc.date.accessioned2014-05-27T11:22:21Z-
dc.date.accessioned2016-10-25T18:23:24Z-
dc.date.available2014-05-27T11:22:21Z-
dc.date.available2016-10-25T18:23:24Z-
dc.date.issued2007-01-01-
dc.identifierhttp://dx.doi.org/10.1002/cbf.1351-
dc.identifier.citationCell Biochemistry and Function, v. 25, n. 1, p. 109-114, 2007.-
dc.identifier.issn0263-6484-
dc.identifier.issn1099-0844-
dc.identifier.urihttp://hdl.handle.net/11449/69436-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69436-
dc.description.abstractThe eukaryotic translation initiation factor 5A (eIF5A) undergoes a specific post-translational modification called hypusination. This modification is required for the functionality of this protein. The compound N1-guanyl-1,7-diaminoheptane (GC7) is a potent and selective inhibitor of deoxyhypusine synthase, which catalyses the first step of eIF5A hypusination process. In the present study, the effects of GC7 on cell death were investigated using two cell lines: melan-a murine melanocytes and Tm5 marine melanoma. In vitro treatment with GC7 increased by 3-fold the number of cells presenting DNA fragmentation in Tm5 cells. Exposure to GC7 also decreased viability to both cell lines. This study also describes, for the first time, the in vivo antitumour effect of GC7, as indicated by impaired melanoma growth in C57BL/6 mice. Copyright © 2006 John Wiley & Sons, Ltd.en
dc.format.extent109-114-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCell proliferation-
dc.subjectCytotoxicity-
dc.subjecteIF-5A-
dc.subjecteIF5A-
dc.subjectGC7-
dc.subjectHypusine-
dc.subjectMelanoma-
dc.subjectTumour growth-
dc.subjectenzyme inhibitor-
dc.subjectinitiation factor 5A-
dc.subjectn1 guanyl 1,7 diaminoheptane-
dc.subjectunclassified drug-
dc.subjectanimal cell-
dc.subjectantineoplastic activity-
dc.subjectcancer growth-
dc.subjectcancer inhibition-
dc.subjectcatalysis-
dc.subjectcell death-
dc.subjectcell viability-
dc.subjectcontrolled study-
dc.subjecthypusination-
dc.subjectmelanoma-
dc.subjectmelanoma cell-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectprotein function-
dc.subjectprotein processing-
dc.subjectAnimals-
dc.subjectCell Line, Tumor-
dc.subjectCell Survival-
dc.subjectDNA Fragmentation-
dc.subjectFemale-
dc.subjectGuanine-
dc.subjectMice-
dc.subjectMice, Inbred C57BL-
dc.subjectMolecular Structure-
dc.subjectPeptide Initiation Factors-
dc.subjectProtein Processing, Post-Translational-
dc.subjectRNA-Binding Proteins-
dc.subjectEukaryota-
dc.subjectMurinae-
dc.subjectMus-
dc.titleInhibition of eukaryotic translation initiation factor 5A (eIF5A) hypusination impairs melanoma growthen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Micro-Immuno-Parasitology Federal University of São Paulo, 04023-062, São Paulo-
dc.description.affiliationDepartment of Physiology and Biophysics Institute of Biomedical Sciences University of São Paulo, 05508-900, São Paulo-
dc.description.affiliationDepartment of Biochemistry and Immunology Faculty of Medicine of Ribeirão Preto University of São Paulo, 14049-900, Ribeirão Preto-
dc.description.affiliationDepartment of Physiology and Pathology Faculty of Dentistry of Araraquara UNESP, 14801-903, Araraquara-
dc.description.affiliationDepartment of Biochemistry and Immunology Faculty of Medicine of Ribeirão Preto University of São Paulo, Av. Bandeirantes 3900, 14049-900, Ribeirao-Preto-
dc.description.affiliationUnespDepartment of Physiology and Pathology Faculty of Dentistry of Araraquara UNESP, 14801-903, Araraquara-
dc.identifier.doi10.1002/cbf.1351-
dc.identifier.wosWOS:000243581300012-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofCell Biochemistry and Function-
dc.identifier.scopus2-s2.0-33846292223-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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