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dc.contributor.authorOtaegui Bichot, David
dc.contributor.authorBaranzini, Sergio E.
dc.contributor.authorArmañanzas Arnedillo, Rubén
dc.contributor.authorCalvo Molinos, Borja ORCID
dc.contributor.authorMuñoz-Culla, Maider
dc.contributor.authorKhankhanian, Puya
dc.contributor.authorInza Cano, Iñaki ORCID
dc.contributor.authorLozano Alonso, José Antonio
dc.contributor.authorCastillo Triviño, Tamara
dc.contributor.authorAsensio, Ana
dc.contributor.authorOlaskoaga, Javier
dc.contributor.authorLópez de Munain Arregui, Adolfo José
dc.date.accessioned2011-06-13T15:01:48Z
dc.date.available2011-06-13T15:01:48Z
dc.date.issued2009-07-20
dc.identifier.citationPLoS ONE 4(7) : (2009) // e6309es
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/4193
dc.description9 p.es
dc.description.abstractDifferences in gene expression patterns have been documented not only in Multiple Sclerosis patients versus healthy controls but also in the relapse of the disease. Recently a new gene expression modulator has been identified: the microRNA or miRNA. The aim of this work is to analyze the possible role of miRNAs in multiple sclerosis, focusing on the relapse stage. We have analyzed the expression patterns of 364 miRNAs in PBMC obtained from multiple sclerosis patients in relapse status, in remission status and healthy controls. The expression patterns of the miRNAs with significantly different expression were validated in an independent set of samples. In order to determine the effect of the miRNAs, the expression of some predicted target genes of these were studied by qPCR. Gene interaction networks were constructed in order to obtain a co-expression and multivariate view of the experimental data. The data analysis and later validation reveal that two miRNAs (hsa-miR-18b and hsa-miR-599) may be relevant at the time of relapse and that another miRNA (hsa-miR-96) may be involved in remission. The genes targeted by hsa-miR-96 are involved in immunological pathways as Interleukin signaling and in other pathways as wnt signaling. This work highlights the importance of miRNA expression in the molecular mechanisms implicated in the disease. Moreover, the proposed involvement of these small molecules in multiple sclerosis opens up a new therapeutic approach to explore and highlight some candidate biomarker targets in MS.es
dc.description.sponsorshipThis work was funded by the ILUNDAIN Fundazioa, by a grant from the Departamento de Sanidad, Gobierno Vasco (2007111054) and by a grant from the Diputación de Gipuzkoa. The computational part of this work has been partially supported by the 2007-2012 Etortek, Saiotek and Research Group (IT-242-07) programs (Basque Government), TIN2005-06815-CO1 and Consolider Ingenio 2010 - CSD2007-00018 projects (Spanish Ministry of Education and Science) and the COMBIOMED network in computational biomedicine (Carlos III Health Institute). R. Armañanzas would like to thank the Basque Government for funding his research (Grant AE-BFI-05/430). M. Muñoz has a fellowship from the ILUNDAIN Fundatioa.es
dc.language.isoenges
dc.publisherPublic Library of Sciencees
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.titleDifferential Micro RNA Expression in PBMC from Multiple Sclerosis Patientses
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2009 Otaegui et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.relation.publisherversionhttp://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0006309es
dc.identifier.doi10.1371/journal.pone.0006309
dc.departamentoesCiencia de la computación e inteligencia artificiales_ES
dc.departamentoeuKonputazio zientziak eta adimen artifizialaes_ES
dc.subject.categoriaAGRICULTURAL AND BIOLOGICAL SCIENCES
dc.subject.categoriaMEDICINE
dc.subject.categoriaBIOCHEMISTRY AND MOLECULAR BIOLOGY


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