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dc.contributor.authorLopes, Tiago Falcónpt_BR
dc.contributor.authorFreitas, Martiela Vaz dept_BR
dc.contributor.authorMello, Ana Carolina de Moraespt_BR
dc.contributor.authorCoutinho, Laura Bezerrapt_BR
dc.contributor.authorÁlvares-da-Silva, Mário Reispt_BR
dc.contributor.authorMatte, Ursula da Silveirapt_BR
dc.date.accessioned2018-10-27T03:12:23Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn2314-6141pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/184033pt_BR
dc.description.abstractHepatocellular carcinoma (HCC) is the prevalent type of primary liver malignancy. Different noncoding RNAs (ncRNAs) that negatively regulate gene expression, such as the microRNAs and the long ncRNAs (lncRNAs), have been associated with cell invasiveness and cell dissemination, tumor recurrence, and metastasis inHCC.To evaluatewhich regulatory ncRNAsmight be good candidates to disrupt HCC proliferation pathways, we performed both unsupervised and supervised analyses of HCC expression data, comparing samples of solid tumor tissue (TP) and adjacent tissue (NT) of a set of patients, focusing on ncRNAs and searching for common mechanisms that may shed light in future therapeutic options. All analyses were performed using the R software. Differential expression (total RNA and miRNA) and enrichment analyses (Gene Ontology + Pathways) were performed using the package TCGABiolinks. As a result, we improved the set of lncRNAs that could be the target of future studies in HCC, highlighting the potential of FAM170B-AS1 and TTN-AS1.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofBiomed research international. New York. Vol. 2018 (2018), 2864120, 9 p.pt_BR
dc.rightsOpen Accessen
dc.subjectCarcinoma hepatocelularpt_BR
dc.subjectExpressão gênicapt_BR
dc.subjectRNA longo não codificantept_BR
dc.subjectHepaciviruspt_BR
dc.subjectVirus da hepatite Bpt_BR
dc.titleAnalysis of the cancer genome atlas data reveals novel putative ncRNAs targets in hepatocellular carcinomapt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001078974pt_BR
dc.type.originEstrangeiropt_BR


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