Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors

Detalhes bibliográficos
Autor(a) principal: Galrao, Ana Luiza Resende
Data de Publicação: 2014
Outros Autores: Camargo, Rosalinda Yossie Asato de, Friguglietti, Celso Ubirajara, Moraes, Lais de Sousa [UNIFESP], Cerutti, Janete Maria [UNIFESP], Serrano-Nascimento, Caroline, Suzuki, Miriam Fussae, Medeiros-Neto, Geraldo, Rubio, Ileana Gabriela Sanchez de [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://dx.doi.org/10.1210/jc.2013-1450
https://repositorio.unifesp.br/handle/11600/37804
Resumo: Context: in thyroid tumors, reduced radioiodine uptake is associated with worse patient outcome concomitantly with low sodium/iodide symporter (NIS) mRNA expression. Previous studies showed that CpG-island methylation in the NIS proximal promoter does not correlate with mRNA expression.Objectives: the aim of the study was to identify new CpG-islands within the NIS 5' region and investigate the involvement of their methylation in NIS expression.Design: DNA was obtained from 30 pairs of thyroid samples: tumor (T) and surrounding nontumor (NT) samples. All T samples had reduced NIS mRNA expression compared to NT samples.Main Outcome Measures: Methylation degree was quantified by bisulfite sequencing, and NIS expression by real-time PCR and Western blot. Reporter gene assays were performed to determine CpG-island functionality. Tumor cell cultures were treated with 5-Aza demethylating agent to determine NIS expression, methylation status, and I-125 uptake.Results: We identified a new CpG-island2 with 14 CpG sites, located -2152/-1887 relative to ATG site. CpG-island2 was hypermethylated in T compared to NT samples, in both benign and malignant tumor groups. There was a significant inverse correlation between NIS mRNA expression and degree of CpG-island2 methylation in NT and T samples. This sequence increased the expression of a reporter gene; thus, it was considered a new enhancer. Cell culture treatments with 5-Aza reduced CpG-island2 methylation levels concomitantly with restoration of NIS mRNA and protein expression and I-125 uptake.Conclusions: We identified a new distal enhancer, NIS distal enhancer, that regulates gene expression through DNA methylation. This enhancer is hypermethylated in T compared to NT samples and is associated with decreased NIS expression in tumors. This epigenetic deregulation may be an early event in tumorigenesis.
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spelling Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid TumorsContext: in thyroid tumors, reduced radioiodine uptake is associated with worse patient outcome concomitantly with low sodium/iodide symporter (NIS) mRNA expression. Previous studies showed that CpG-island methylation in the NIS proximal promoter does not correlate with mRNA expression.Objectives: the aim of the study was to identify new CpG-islands within the NIS 5' region and investigate the involvement of their methylation in NIS expression.Design: DNA was obtained from 30 pairs of thyroid samples: tumor (T) and surrounding nontumor (NT) samples. All T samples had reduced NIS mRNA expression compared to NT samples.Main Outcome Measures: Methylation degree was quantified by bisulfite sequencing, and NIS expression by real-time PCR and Western blot. Reporter gene assays were performed to determine CpG-island functionality. Tumor cell cultures were treated with 5-Aza demethylating agent to determine NIS expression, methylation status, and I-125 uptake.Results: We identified a new CpG-island2 with 14 CpG sites, located -2152/-1887 relative to ATG site. CpG-island2 was hypermethylated in T compared to NT samples, in both benign and malignant tumor groups. There was a significant inverse correlation between NIS mRNA expression and degree of CpG-island2 methylation in NT and T samples. This sequence increased the expression of a reporter gene; thus, it was considered a new enhancer. Cell culture treatments with 5-Aza reduced CpG-island2 methylation levels concomitantly with restoration of NIS mRNA and protein expression and I-125 uptake.Conclusions: We identified a new distal enhancer, NIS distal enhancer, that regulates gene expression through DNA methylation. This enhancer is hypermethylated in T compared to NT samples and is associated with decreased NIS expression in tumors. This epigenetic deregulation may be an early event in tumorigenesis.Univ São Paulo, Sch Med FM USP, Cellular & Mol Endocrine Lab, Thyroid Unit, BR-01246903 São Paulo, BrazilHead & Neck Surg Santa Catarina Hosp, BR-01310000 São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Dept Morphol & Genet, Div Genet, Genet Bases Thyroid Tumors Lab, BR-04039032 São Paulo, BrazilUniv São Paulo, Inst Biomed Sci, Dept Physiol & Biophys, BR-05508900 São Paulo, BrazilIPEN CNEN SP, Inst Pesquisas Energet & Nucl, Ctr Biotechnol, BR-05508000 São Paulo, BrazilUNIFESP, Dept Biol Sci, BR-09972270 Diadema, SP, BrazilUniversidade Federal de São Paulo UNIFESP, Dept Morphol & Genet, Div Genet, Genet Bases Thyroid Tumors Lab, BR-04039032 São Paulo, BrazilUNIFESP, Dept Biol Sci, BR-09972270 Diadema, SP, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Instituto da Tiroide, São Paulo, BrazilFAPESP: 2007/51235-7FAPESP: 2007/51236-3FAPESP: 2009/52517-1Endocrine SocUniversidade de São Paulo (USP)Head & Neck Surg Santa Catarina HospUniversidade Federal de São Paulo (UNIFESP)IPEN CNEN SPGalrao, Ana Luiza ResendeCamargo, Rosalinda Yossie Asato deFriguglietti, Celso UbirajaraMoraes, Lais de Sousa [UNIFESP]Cerutti, Janete Maria [UNIFESP]Serrano-Nascimento, CarolineSuzuki, Miriam FussaeMedeiros-Neto, GeraldoRubio, Ileana Gabriela Sanchez de [UNIFESP]2016-01-24T14:37:20Z2016-01-24T14:37:20Z2014-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionE944-E952https://dx.doi.org/10.1210/jc.2013-1450Journal of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 99, n. 6, p. E944-E952, 2014.10.1210/jc.2013-14500021-972Xhttps://repositorio.unifesp.br/handle/11600/37804WOS:000342340500002engJournal of Clinical Endocrinology & Metabolisminfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-10T20:50:57Zoai:repositorio.unifesp.br/:11600/37804Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-10T20:50:57Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
title Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
spellingShingle Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
Galrao, Ana Luiza Resende
title_short Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
title_full Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
title_fullStr Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
title_full_unstemmed Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
title_sort Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
author Galrao, Ana Luiza Resende
author_facet Galrao, Ana Luiza Resende
Camargo, Rosalinda Yossie Asato de
Friguglietti, Celso Ubirajara
Moraes, Lais de Sousa [UNIFESP]
Cerutti, Janete Maria [UNIFESP]
Serrano-Nascimento, Caroline
Suzuki, Miriam Fussae
Medeiros-Neto, Geraldo
Rubio, Ileana Gabriela Sanchez de [UNIFESP]
author_role author
author2 Camargo, Rosalinda Yossie Asato de
Friguglietti, Celso Ubirajara
Moraes, Lais de Sousa [UNIFESP]
Cerutti, Janete Maria [UNIFESP]
Serrano-Nascimento, Caroline
Suzuki, Miriam Fussae
Medeiros-Neto, Geraldo
Rubio, Ileana Gabriela Sanchez de [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Head & Neck Surg Santa Catarina Hosp
Universidade Federal de São Paulo (UNIFESP)
IPEN CNEN SP
dc.contributor.author.fl_str_mv Galrao, Ana Luiza Resende
Camargo, Rosalinda Yossie Asato de
Friguglietti, Celso Ubirajara
Moraes, Lais de Sousa [UNIFESP]
Cerutti, Janete Maria [UNIFESP]
Serrano-Nascimento, Caroline
Suzuki, Miriam Fussae
Medeiros-Neto, Geraldo
Rubio, Ileana Gabriela Sanchez de [UNIFESP]
description Context: in thyroid tumors, reduced radioiodine uptake is associated with worse patient outcome concomitantly with low sodium/iodide symporter (NIS) mRNA expression. Previous studies showed that CpG-island methylation in the NIS proximal promoter does not correlate with mRNA expression.Objectives: the aim of the study was to identify new CpG-islands within the NIS 5' region and investigate the involvement of their methylation in NIS expression.Design: DNA was obtained from 30 pairs of thyroid samples: tumor (T) and surrounding nontumor (NT) samples. All T samples had reduced NIS mRNA expression compared to NT samples.Main Outcome Measures: Methylation degree was quantified by bisulfite sequencing, and NIS expression by real-time PCR and Western blot. Reporter gene assays were performed to determine CpG-island functionality. Tumor cell cultures were treated with 5-Aza demethylating agent to determine NIS expression, methylation status, and I-125 uptake.Results: We identified a new CpG-island2 with 14 CpG sites, located -2152/-1887 relative to ATG site. CpG-island2 was hypermethylated in T compared to NT samples, in both benign and malignant tumor groups. There was a significant inverse correlation between NIS mRNA expression and degree of CpG-island2 methylation in NT and T samples. This sequence increased the expression of a reporter gene; thus, it was considered a new enhancer. Cell culture treatments with 5-Aza reduced CpG-island2 methylation levels concomitantly with restoration of NIS mRNA and protein expression and I-125 uptake.Conclusions: We identified a new distal enhancer, NIS distal enhancer, that regulates gene expression through DNA methylation. This enhancer is hypermethylated in T compared to NT samples and is associated with decreased NIS expression in tumors. This epigenetic deregulation may be an early event in tumorigenesis.
publishDate 2014
dc.date.none.fl_str_mv 2014-06-01
2016-01-24T14:37:20Z
2016-01-24T14:37:20Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://dx.doi.org/10.1210/jc.2013-1450
Journal of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 99, n. 6, p. E944-E952, 2014.
10.1210/jc.2013-1450
0021-972X
https://repositorio.unifesp.br/handle/11600/37804
WOS:000342340500002
url https://dx.doi.org/10.1210/jc.2013-1450
https://repositorio.unifesp.br/handle/11600/37804
identifier_str_mv Journal of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 99, n. 6, p. E944-E952, 2014.
10.1210/jc.2013-1450
0021-972X
WOS:000342340500002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Clinical Endocrinology & Metabolism
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv E944-E952
dc.publisher.none.fl_str_mv Endocrine Soc
publisher.none.fl_str_mv Endocrine Soc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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