TCF21/POD-1, a transcritional regulator of SF-1/NR5A1, as a potential prognosis marker in adult and pediatric adrenocortical tumors

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dc.contributor(LETA) Lab. Toxinologia Aplicadapt_BR
dc.contributor.authorPassaia, Barbara dos Santospt_BR
dc.contributor.authorDias, Matheus Henriquept_BR
dc.contributor.authorKremer, Jean Lucaspt_BR
dc.contributor.authorRauber Antonini, Sonir Robertopt_BR
dc.contributor.authorde Almeida, Madson Queirozpt_BR
dc.contributor.authorBarisson Villares Fragoso, Maria Candidapt_BR
dc.contributor.authorPacicco Lotfi, Claudimara Ferinipt_BR
dc.date.accessioned2020-07-09T21:19:28Z-
dc.date.available2020-07-09T21:19:28Z-
dc.date.issued2018pt_BR
dc.identifier.citationPassaia BS, Dias MH, Kremer JL, Rauber Antonini SR, de Almeida MQ, Barisson Villares Fragoso MC, et al. TCF21/POD-1, a transcritional regulator of SF-1/NR5A1, as a potential prognosis marker in adult and pediatric adrenocortical tumors. Front Endocrinol. 2018 Feb;9:38. doi:10.3389/fendo.2018.00038.pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/2421-
dc.description.abstractWith recent progress in understanding the pathogenesis of adrenocortical tumors (ACTs), identification of molecular markers to predict their prognosis has become possible. Transcription factor 21 (TCF21)/podocyte-expressed 1 (POD1) is a transcriptional regulatory protein expressed in mesenchymal cells at sites of epithelial-mesenchymal transition during the development of different systems. Adult carcinomas express less TCF21 than adenomas, in addition, the KEGG pathway analysis has shown that BUB1B, among others genes, is negatively correlated with TCF21 expression. The difference between BUB1B and PTEN-induced putative kinase 1 (PINK1) expression has been described previously to be associated with survival in adult but not in pediatric carcinomas. Here, we analyzed the gene expression of TCF21, BUB1B, PINK1, and NR5A1 in adult and pediatric ACTs. We found a negative correlation between the relative expression levels of TCF21 and BUB1B in adult ACTs, but the relative expression levels of TCF21, BUB1B, PINK1, and NR5A1 were similar in childhood ACTs. In addition, we propose using the subtracted expression levels of the TCF21/POD-1 genes as a predictor of overall survival (OS) in adult carcinomas and TCF21-NR5A1 as a predictor of malignancy for pediatric tumors in patients aged <5 years. These results require further validation in different cohorts of both adult and pediatric samples. Finally, we observed that the OS for patients aged <5 years was markedly favorable compared with that for patients >5 years as well as adult patients with carcinoma. In summary, we propose TCF21/POD-1 as a new prognostic marker in adult and pediatric ACTs.pt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.format.extent38pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofFrontiers in Endocrinologypt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleTCF21/POD-1, a transcritional regulator of SF-1/NR5A1, as a potential prognosis marker in adult and pediatric adrenocortical tumorspt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.identifier.doi10.3389/fendo.2018.00038pt_BR
dc.contributor.external(USP) Universidade de São Paulopt_BR
dc.identifier.citationvolume9pt_BR
dc.subject.keywordadrenocortical tumorspt_BR
dc.subject.keywordadult and pediatric tumorspt_BR
dc.subject.keywordtranscription factor 21pt_BR
dc.subject.keywordpodocyte-expressed 1pt_BR
dc.subject.keywordBUB1Bpt_BR
dc.subject.keywordPTEN-induced putative kinase 1pt_BR
dc.subject.keywordnuclear receptor subfamily 5 group A member 1pt_BR
dc.subject.keywordCRISPR/dCas9pt_BR
dc.relation.ispartofabbreviatedFront Endocrinolpt_BR
dc.identifier.citationabntv. 9, 38, fev. 2018pt_BR
dc.identifier.citationvancouver2018 Feb;9:38pt_BR
dc.contributor.butantanDias, Matheus Henrique|:Aluno|:(LETA) Lab. Toxinologia Aplicada|:pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2013/235481pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2011/07656-3pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2015/014199-9pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
item.fulltextCom Texto completo-
item.openairetypeArticle-
item.languageiso639-1English-
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