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dc.contributor.CRUESPUniversidade Estadual de Campinaspt_BR
dc.typeArtigo de periódicopt_BR
dc.titleLeucine modulates the effect of Walker factor, a proteolysis-inducing factor-like protein from Walker tumours, on gene expression and cellular activity in C2C12 myotubespt_BR
dc.contributor.authorGoncalves, EMpt_BR
dc.contributor.authorSalomao, EMpt_BR
dc.contributor.authorGomes-Marcondes, MCCpt_BR
unicamp.author.emailcintgoma@unicamp.brpt_BR
unicamp.authorGoncalves, Estela Maria Salomao, Emilianne Miguel Cintra Gomes-Marcondes, Maria Cristina State Univ Campinas UNICAMP, Inst Biol, Dept Struct & Funct Biol, BR-13083970 Campinas, SP, Brazilpt_BR
dc.subjectCancer cachexiapt_BR
dc.subjectLeucinept_BR
dc.subjectProteolysis-inducing factorpt_BR
dc.subjectWalker factorpt_BR
dc.subjectWalker 256 tumourpt_BR
dc.subject.wosSkeletal-muscle Proteolysispt_BR
dc.subject.wosCancer Cachectic Factorpt_BR
dc.subject.wosUbiquitin-dependent Proteolysispt_BR
dc.subject.wosBearing Ratspt_BR
dc.subject.wosAmino-acidspt_BR
dc.subject.wosWeight-losspt_BR
dc.subject.wosIn-vitropt_BR
dc.subject.wosTranslation Initiationpt_BR
dc.subject.wosIntestinal-absorptionpt_BR
dc.subject.wosProteasome Activitypt_BR
dc.description.abstractCancer-cachexia causes severe weight loss, particularly from the wasting of skeletal muscle, which occurs due to increased protein catabolism and/or decreased protein synthesis. The muscle protein degradation observed in cancer patients is mediated by a specific cytokine, proteolysis-inducing factor (PIF), which is produced by the tumour. This protein increases the ubiquitin-proteasome pathway activity, and the synthesis of muscle protein in these patients can be affected by several factors, including nutrient-related signalling. Some nutrients, such as leucine, can decrease the ubiquitin-proteasome pathway activity and increase the skeletal muscle protein content in cachectic animals. In this study, we investigated the effects of leucine on cell viability, morphology, functional proteasome activity, enzymatic activity, and protein synthesis and degradation in C2C12 myotubes exposed to the proteolysis-inducing factor (PIF)-like protein purified from Walker tumour-bearing rats. Walker factor (WF) had no cytotoxic effects on myotube cells and morphological characteristics were not altered in the presence of WF and/or leucine. However, increased alkaline phosphatase activity was observed. At higher WE concentrations, chymotrypsin-like activity, cathepsin B activity and 20S proteasome gene expression increased. Treating myotubes with leucine before exposure to WF causes leads to a decrease in proteasome activity as well as the activity of chymotrypsin and cathepsin enzymes. Total protein synthesis decreased in WF-treated cells concomitantly as protein degradation increased. After leucine exposure, the observed effects of WF were minimal or even reverted in some cases. Taken together, these results suggest an important modulatory effect for leucine on the effects of WF in C2C12 myotube cells. (C) 2013 Elsevier Ltd. All rights reserved.pt
dc.relation.ispartofCytokinept_BR
dc.relation.ispartofabbreviationCytokinept_BR
dc.publisher.cityLondonpt_BR
dc.publisher.countryInglaterrapt_BR
dc.publisherAcademic Press Ltd- Elsevier Science Ltdpt_BR
dc.date.issued2013pt_BR
dc.date.monthofcirculationOCTpt_BR
dc.identifier.citationCytokine. Academic Press Ltd- Elsevier Science Ltd, v. 64, n. 1, n. 343, n. 350, 2013.pt_BR
dc.language.isoenpt_BR
dc.description.volume64pt_BR
dc.description.issuenumber1pt_BR
dc.description.firstpage343pt_BR
dc.description.lastpage350pt_BR
dc.rightsfechadopt_BR
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policypt_BR
dc.sourceWeb of Sciencept_BR
dc.identifier.issn1043-4666pt_BR
dc.identifier.eissn1096-0023pt_BR
dc.identifier.wosidWOS:000325442700050pt_BR
dc.identifier.doi10.1016/j.cyto.2013.05.018pt_BR
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsorship1Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorship1Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt_BR
dc.description.sponsordocumentnumberFAPESP [2010/00260-4, 2010/11328-9]pt
dc.description.sponsordocumentnumberCNPq [304604/2010-0, 502915/2007-2]pt
dc.date.available2014-08-01T18:34:01Z
dc.date.available2015-11-26T18:03:19Z-
dc.date.accessioned2014-08-01T18:34:01Z
dc.date.accessioned2015-11-26T18:03:19Z-
dc.description.provenanceMade available in DSpace on 2014-08-01T18:34:01Z (GMT). No. of bitstreams: 0 Previous issue date: 2013en
dc.description.provenanceMade available in DSpace on 2015-11-26T18:03:19Z (GMT). No. of bitstreams: 0 Previous issue date: 2013en
dc.identifier.urihttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/80864
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/80864-
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