Hypermethylation of a New Distal Sodium/Iodide Symporter (NIS) Enhancer (NDE) Is Associated With Reduced NIS Expression in Thyroid Tumors
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , |
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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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 |
_version_ |
1814268401236836352 |