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dc.contributor.authorBerdasco, María
dc.contributor.authorGómez, Antonio
dc.contributor.authorRubio, Marcos J
dc.contributor.authorCatalà-Mora, Jaume
dc.contributor.authorZanón-Moreno, Vicente
dc.contributor.authorLopez, Miguel
dc.contributor.authorHernández, Cristina
dc.contributor.authorYoshida, Shigeo
dc.contributor.authorNakama, Takahito
dc.contributor.authorIshikawa, Keijiro
dc.contributor.authorIshibashi, Tatsuro
dc.contributor.authorBoubekeur, Amina M
dc.contributor.authorLouhibi, Lotfi
dc.contributor.authorPujana, Miguel A
dc.contributor.authorSayols, Sergi
dc.contributor.authorSetien, Fernando
dc.contributor.authorCorella, Dolores
dc.contributor.authorde Torres, Carmen
dc.contributor.authorParareda, Andreu
dc.contributor.authorMora, Jaume
dc.contributor.authorZhao, Ling
dc.contributor.authorZhang, Kang
dc.contributor.authorLleonart, Matilde E
dc.contributor.authorAlonso, Javier 
dc.contributor.authorSimó, Rafael
dc.contributor.authorCaminal, Josep M
dc.contributor.authorEsteller, Manel
dc.date.accessioned2020-02-26T17:42:09Z
dc.date.available2020-02-26T17:42:09Z
dc.date.issued2017
dc.identifier.citationSci Rep. 2017 Sep 18;7(1):11762.es_ES
dc.identifier.issn2045-2322es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/9150
dc.description.abstractThis work provides a comprehensive CpG methylation landscape of the different layers of the human eye that unveils the gene networks associated with their biological functions and how these are disrupted in common visual disorders. Herein, we firstly determined the role of CpG methylation in the regulation of ocular tissue-specification and described hypermethylation of retinal transcription factors (i.e., PAX6, RAX, SIX6) in a tissue-dependent manner. Second, we have characterized the DNA methylome of visual disorders linked to internal and external environmental factors. Main conclusions allow certifying that crucial pathways related to Wnt-MAPK signaling pathways or neuroinflammation are epigenetically controlled in the fibrotic disorders involved in retinal detachment, but results also reinforced the contribution of neurovascularization (ETS1, HES5, PRDM16) in diabetic retinopathy. Finally, we had studied the methylome in the most frequent intraocular tumors in adults and children (uveal melanoma and retinoblastoma, respectively). We observed that hypermethylation of tumor suppressor genes is a frequent event in ocular tumors, but also unmethylation is associated with tumorogenesis. Interestingly, unmethylation of the proto-oncogen RAB31 was a predictor of metastasis risk in uveal melanoma. Loss of methylation of the oncogenic mir-17-92 cluster was detected in primary tissues but also in blood from patients.es_ES
dc.description.sponsorshipThe research leading to these results was supported by European Research Council Advanced Grant EPINORC, RecerCaixa Foundation, Federación Española de Enfermedades Raras (FEDER), Federación Española de Enfermedades Neuromusculares (ASEM), Fundación Isabel Gemio, COST CM1406, Instituto de Salud Carlos III (PI/00816) and Health and Sciences Departments of the Catalan Government (Generalitat de Catalunya). M.E. is an Institució Catalana de Recerca i Estudis Avançats (ICREA) Research Professor. We thank the staff of the Biobank Facility at the Bellvitge Biomedical Research Institute (IDIBELL), Spanish National Cancer Research Center (CNIO), Institute of Rare Diseases Research (BioNER-ISCIII), Vall d’Hebron Research Institute (VHIR) and Banc de Sang i Teixits (BST) of the Catalan Ministry of Health. We also thank Dr. Mercedes Hurtado (Department of Ophthalmology, University and Polytechnic Hospital La Fe) and Dr. Dolores Pinazo (Department of Ophthalmology, Dr. Peset University Hospital) for obtaining samples from glaucomatous patients. We thank the patients and their families.es_ES
dc.language.isoenges_ES
dc.publisherNature Researches_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAdult es_ES
dc.subject.meshChild es_ES
dc.subject.meshChild, Preschool es_ES
dc.subject.meshEye Neoplasms es_ES
dc.subject.meshFemale es_ES
dc.subject.meshHumans es_ES
dc.subject.meshMale es_ES
dc.subject.meshDNA Methylation es_ES
dc.subject.meshDNA, Neoplasm es_ES
dc.subject.meshDiabetic Retinopathy es_ES
dc.subject.meshEpigenesis, Genetices_ES
dc.subject.meshEye es_ES
dc.subject.meshEye Proteins es_ES
dc.subject.meshGene Expression Regulation, Neoplastic es_ES
dc.subject.meshMAP Kinase Signaling System es_ES
dc.subject.meshNeoplasm Proteins es_ES
dc.subject.meshRetinal Neovascularization es_ES
dc.titleDNA Methylomes Reveal Biological Networks Involved in Human Eye Development, Functions and Associated Disorderses_ES
dc.typeArtículoes_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID28924151es_ES
dc.format.volume7es_ES
dc.format.number1es_ES
dc.format.page11762es_ES
dc.identifier.doi10.1038/s41598-017-12084-1es_ES
dc.contributor.funderRecercaixaes_ES
dc.contributor.funderFederación Española de Enfermedades Rarases_ES
dc.contributor.funderInstituto de Salud Carlos III - ISCIIIes_ES
dc.contributor.funderGeneralitat de Catalunyaes_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn2045-2322es_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41598-017-12084-1es_ES
dc.identifier.journalScientific reportses_ES
dc.repisalud.centroISCIII::Instituto de Investigación de Enfermedades Rarases_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI/00816es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Atribución 4.0 Internacional
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