In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.

Detalhes bibliográficos
Autor(a) principal: PEREIRA, C. M.
Data de Publicação: 2018
Outros Autores: CARVALHO, A. C. de, SILVA, F. R. da, MELENDEZ, M. E., LESSA, R. C., ANDRADE, V. C. C., KOWALSKI, L. P., VETTORE, A. L., CARVALHO, A. L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
Texto Completo: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692
https://doi.org/10.1186/s12885-018-4077-3
Resumo: Abstract. 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.
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spelling In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.Expressão gênicaORESTESCarcinogêneseValidação in vitroValidação in silicoOpen reading expressed sequence tagsOral squamous cell carcinomaMetilaçãoGene expressionMethylationAbstract. 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.Article number: 193.CLÁUDIA 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.PEREIRA, C. M.CARVALHO, A. C. deSILVA, F. R. daMELENDEZ, M. E.LESSA, R. C.ANDRADE, V. C. C.KOWALSKI, L. P.VETTORE, A. L.CARVALHO, A. L.2020-01-07T18:10:32Z2020-01-07T18:10:32Z2019-02-0720182020-01-07T18:10:32Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleBMC Cancer, v. 18, p. 1-10, 2018.http://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692https://doi.org/10.1186/s12885-018-4077-3enginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)instacron:EMBRAPA2020-01-07T18:10:38Zoai:www.alice.cnptia.embrapa.br:doc/1105692Repositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestopendoar:21542020-01-07T18:10:38falseRepositório InstitucionalPUBhttps://www.alice.cnptia.embrapa.br/oai/requestcg-riaa@embrapa.bropendoar:21542020-01-07T18:10:38Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)false
dc.title.none.fl_str_mv In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
title In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
spellingShingle In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
PEREIRA, C. M.
Expressão gênica
ORESTES
Carcinogênese
Validação in vitro
Validação in silico
Open reading expressed sequence tags
Oral squamous cell carcinoma
Metilação
Gene expression
Methylation
title_short In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
title_full In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
title_fullStr In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
title_full_unstemmed In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
title_sort In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
author PEREIRA, C. M.
author_facet PEREIRA, C. M.
CARVALHO, A. C. de
SILVA, F. R. da
MELENDEZ, M. E.
LESSA, R. C.
ANDRADE, V. C. C.
KOWALSKI, L. P.
VETTORE, A. L.
CARVALHO, A. L.
author_role author
author2 CARVALHO, A. C. de
SILVA, F. R. da
MELENDEZ, M. E.
LESSA, R. C.
ANDRADE, V. C. C.
KOWALSKI, L. P.
VETTORE, A. L.
CARVALHO, A. L.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv CLÁUDIA 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.
dc.contributor.author.fl_str_mv PEREIRA, C. M.
CARVALHO, A. C. de
SILVA, F. R. da
MELENDEZ, M. E.
LESSA, R. C.
ANDRADE, V. C. C.
KOWALSKI, L. P.
VETTORE, A. L.
CARVALHO, A. L.
dc.subject.por.fl_str_mv Expressão gênica
ORESTES
Carcinogênese
Validação in vitro
Validação in silico
Open reading expressed sequence tags
Oral squamous cell carcinoma
Metilação
Gene expression
Methylation
topic Expressão gênica
ORESTES
Carcinogênese
Validação in vitro
Validação in silico
Open reading expressed sequence tags
Oral squamous cell carcinoma
Metilação
Gene expression
Methylation
description Abstract. 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.
publishDate 2018
dc.date.none.fl_str_mv 2018
2019-02-07
2020-01-07T18:10:32Z
2020-01-07T18:10:32Z
2020-01-07T18:10:32Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv BMC Cancer, v. 18, p. 1-10, 2018.
http://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692
https://doi.org/10.1186/s12885-018-4077-3
identifier_str_mv BMC Cancer, v. 18, p. 1-10, 2018.
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1105692
https://doi.org/10.1186/s12885-018-4077-3
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
instname:Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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instname_str Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
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reponame_str Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
collection Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice)
repository.name.fl_str_mv Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) - Empresa Brasileira de Pesquisa Agropecuária (Embrapa)
repository.mail.fl_str_mv cg-riaa@embrapa.br
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