Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692
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dc.contributor.authorPEREIRA, C. M.eng
dc.contributor.authorCARVALHO, A. C. deeng
dc.contributor.authorSILVA, F. R. daeng
dc.contributor.authorMELENDEZ, M. E.eng
dc.contributor.authorLESSA, R. C.eng
dc.contributor.authorANDRADE, V. C. C.eng
dc.contributor.authorKOWALSKI, L. P.eng
dc.contributor.authorVETTORE, A. L.eng
dc.contributor.authorCARVALHO, A. L.eng
dc.date.accessioned2020-01-07T18:10:32Z-
dc.date.available2020-01-07T18:10:32Z-
dc.date.created2019-02-07
dc.date.issued2018
dc.identifier.citationBMC Cancer, v. 18, p. 1-10, 2018.eng
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692-
dc.descriptionAbstract. Background: Aberrant methylation is a frequent event in oral cancer. Methods: In order to better characterize these alterations, a search for genes downregulated by aberrant methylation in oral squamous cell carcinoma (OSCC) was conducted through the mining of ORESTES dataset. Findings were further validated in OSCC cell lines and patients? samples and confirmed using TCGA data. Differentially expressed genes were identified in ORESTES libraries and validated in vitro using RT-PCR in HNSCC cell-lines and OSCC tumor samples. Further confirmation of these results was performed using mRNA expression and methylation data from The Cancer Genome Atlas (TCGA) data. Results: From the set of genes selected for validation, CA3 and FHL1 were downregulated in 60% (12/20) and 75% (15/20) of OSCC samples, respectively, and in HNSCC cell lines. The treatment of cell lines JHU-13 and FaDu with the demethylating agent 5'-aza-dC was efficient in restoring CA3 and FHL1 expression. TCGA expression and methylation data on OSCC confirms the downregulation of these genes in OSCC samples and also suggests that expression of CA3 and FHL1 is probably regulated by methylation. The downregulation of CA3 and FHL1 observed in silico was validated in HNSCC cell lines and OSCC samples, showing the feasibility of integrating different datasets to select differentially expressed genes in silico. Conclusions: These results showed that the downregulation of CA3 and FHL1 data observed in the ORESTES libraries was validated in HNSCC cell lines and OSCC samples and in a large cohort of samples from the TCGA database. Moreover, it suggests that expression of CA3 and FHL1 could probably be regulated by methylation having an important role the oral carcinogenesis.eng
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectExpressão gênicaeng
dc.subjectORESTESeng
dc.subjectCarcinogêneseeng
dc.subjectValidação in vitroeng
dc.subjectValidação in silicoeng
dc.subjectOpen reading expressed sequence tagseng
dc.subjectOral squamous cell carcinomaeng
dc.titleIn vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.eng
dc.typeArtigo de periódicoeng
dc.date.updated2020-01-07T18:10:32Z
dc.subject.thesagroMetilaçãoeng
dc.subject.nalthesaurusGene expressioneng
dc.subject.nalthesaurusMethylationeng
dc.description.notesArticle number: 193.eng
riaa.ainfo.id1105692eng
riaa.ainfo.lastupdate2020-01-07
dc.identifier.doihttps://doi.org/10.1186/s12885-018-4077-3eng
dc.contributor.institutionCLÁUDIA MARIA PEREIRA, A. C. Camargo Cancer Hospital, Ludwig Institute for Cancer Research, São Paulo; ANA CAROLINA DE CARVALHO, Barretos Cancer Hospital, Unifesp; FELIPE RODRIGUES DA SILVA, CNPTIA; MATIAS ELISEO MELENDEZ, Barretos Cancer Hospital; ROBERTA CARDIM LESSA, A. C. Camargo Cancer Hospital, Ludwig Institute for Cancer Research; VALÉRIA CRISTINA C. ANDRADE, Unifesp; LUIZ PAULO KOWALSKI, A. C. Camargo Cancer Hospital; ANDRÉ L. VETTORE, Ludwig Institute for Cancer Research, Unifesp; ANDRÉ LOPES CARVALHO, A. C. Camargo Cancer Hospital, Barretos Cancer Hospital, Barretos.eng
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