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dc.contributor.authorDuran-Sanchon, S.
dc.contributor.authorVila-Navarro, E.
dc.contributor.authorMarcuello, M.
dc.contributor.authorLozano, J. J.
dc.contributor.authorMunoz, J.
dc.contributor.authorCubiella Fernández, Joaquín 
dc.contributor.authorDiez, M. S.
dc.contributor.authorBujanda, L.
dc.contributor.authorLanas, A.
dc.contributor.authorJover, R.
dc.contributor.authorHernández Ramirez, Vicent 
dc.contributor.authorQuintero, E.
dc.contributor.authorHerreros-Villanueva, M.
dc.contributor.authorMartin, A. C.
dc.contributor.authorPerez-Palacios, R.
dc.contributor.authorArroyo, R.
dc.contributor.authorCastells, A.
dc.contributor.authorGironella, M.
dc.date.accessioned2022-01-27T10:40:00Z
dc.date.available2022-01-27T10:40:00Z
dc.date.issued2019
dc.identifier.issn2218-273x
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31877644es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/15956
dc.description.abstractBACKGROUND: Circulating microRNA (miRNA) analysis is a growing research field. However, it usually requires an endogenous control or housekeeping (HK) in order to normalize expression of specific miRNAs throughout different samples. Unfortunately, no adequate HK for circulating miRNA analysis is still known in the colorectal cancer (CRC) context whereas several have been suggested. Hence, our aims were to validate the previously suggested miR-1228-3p as HK for CRC studies, to compare its suitability with the widely used miR-16-5p, and to evaluate the influence of hemolysis on both miRNAs. METHODS: We analyzed by quantitative reverse-transcription polymerase chain reaction (qRT-PCR) the expression of miR-1228-3p, miR-16-5p and the spike-in cel-miR-39 in a set of 297 plasmas (92 CRC, 101 advanced adenomas -AA-, and 100 controls) and 213 serum samples (59 CRC, 74 AA and 80 controls). We also analyzed both miRNAs depending on the hemolysis degree in 7 plasmas and 31 serums. RESULTS: Levels of miR-1228-3p and miR-16-5p did not show significant differences between groups although miR-16-5p exhibited more variability in plasma and serum samples. Importantly, the combination of cel-miR-39 and miR-1228-3p was the most stable one. Moreover, we observed that miR-16-5p was significantly influenced by hemolysis in contrast with miR-1228-3p that exhibited no correlation with this confounding factor in both biofluids. CONCLUSION: MiR-1228-3p has been validated as an adequate endogenous control for circulating miRNA analysis in CRC and AA liquid biopsies.en
dc.language.isoenges
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshMicroRNAs*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshGenes*
dc.subject.meshGene Expression Regulation*
dc.subject.meshAged*
dc.subject.meshColorectal Neoplasms*
dc.titleValidation of miR-1228-3p as Housekeeping for MicroRNA Analysis in Liquid Biopsies from Colorectal Cancer Patientsen
dc.typeArtigoes
dc.identifier.doi10.3390/biom10010016
dc.identifier.pmid31877644
dc.identifier.sophos32659
dc.issue.number1es
dc.journal.titleBiomoleculeses
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Complexo Hospitalario Universitario de Ourense::Complexo Hospitalario Universitario de Ourensees
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Vigo - Complexo Hospitalario Universitario de Vigo::Dixestivoes
dc.relation.publisherversionhttps://res.mdpi.com/d_attachment/biomolecules/biomolecules-10-00016/article_deploy/biomolecules-10-00016-v2.pdfes
dc.rights.accessRightsopenAccesses
dc.subject.decsmicroARN*
dc.subject.decsanciano*
dc.subject.decsgenes*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decsregulación de la expresión génica*
dc.subject.decsneoplasias colorrectales*
dc.subject.keywordCHUOes
dc.subject.keywordCHUVIes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number10es


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Atribución 4.0 Internacional
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