In vitro and in silico validation of CA3 and FHL1 downregulation in oral cancer.
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
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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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 |
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Empresa Brasileira de Pesquisa Agropecuária (Embrapa) |
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EMBRAPA |
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EMBRAPA |
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Repositório Institucional da EMBRAPA (Repository Open Access to Scientific Information from EMBRAPA - Alice) |
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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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1794503487261769728 |