High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1210/jc.2014-4053 http://hdl.handle.net/11449/164900 |
Resumo: | Context: Thyroid nodules are common in adult population and papillary thyroid carcinoma (PTC) is the most frequent malignant finding. The natural history of PTC remains poorly understood and current diagnostic methods limitations are responsible for a significant number of potentially avoidable surgeries. Objective: This study aimed to identify molecular markers to improve the diagnosis of thyroid lesions. Design: Gene expression profiling was performed using microarray in 61 PTC and 13 surrounding normal tissues (NT). A reliable gene list was established using cross-study validation (138 matched PTC/NT from external databases). Results were collectively interpreted by in silico analysis. A panel of 28 transcripts was evaluated by RT-qPCR, including benign thyroid lesions (BTL) and other follicular cell-derived thyroid carcinomas (OFDTC). Adiagnostic algorithm was developed (training set: 23 NT, 8 BTL, and 86 PTC), validated (independent set: 10 NT, 140 BTL, 120 PTC, and 12 OFDTC) and associated with clinical features. Results: GABRB2 was ranked as the most frequently up-regulated gene in PTC (cross-study validation). Altered genes in PTC suggested a loss of T-4 responsiveness and dysregulation of retinoic acid metabolism, highlighting the putative activation of EZH2 and histone deacetylases (predicted in silico). An algorithm combining CLDN10, HMGA2, and LAMB3 transcripts was able to discriminate tumors from BTL samples (94% sensitivity and 96% specificity in validation set). High algorithm scores were associated with regional lymph node metastases. Conclusions: A promising tool with high performance for PTC diagnosis based on three transcripts was designed with the potential to predict lymph node metastasis risk. |
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Repositório Institucional da UNESP |
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High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid CarcinomaContext: Thyroid nodules are common in adult population and papillary thyroid carcinoma (PTC) is the most frequent malignant finding. The natural history of PTC remains poorly understood and current diagnostic methods limitations are responsible for a significant number of potentially avoidable surgeries. Objective: This study aimed to identify molecular markers to improve the diagnosis of thyroid lesions. Design: Gene expression profiling was performed using microarray in 61 PTC and 13 surrounding normal tissues (NT). A reliable gene list was established using cross-study validation (138 matched PTC/NT from external databases). Results were collectively interpreted by in silico analysis. A panel of 28 transcripts was evaluated by RT-qPCR, including benign thyroid lesions (BTL) and other follicular cell-derived thyroid carcinomas (OFDTC). Adiagnostic algorithm was developed (training set: 23 NT, 8 BTL, and 86 PTC), validated (independent set: 10 NT, 140 BTL, 120 PTC, and 12 OFDTC) and associated with clinical features. Results: GABRB2 was ranked as the most frequently up-regulated gene in PTC (cross-study validation). Altered genes in PTC suggested a loss of T-4 responsiveness and dysregulation of retinoic acid metabolism, highlighting the putative activation of EZH2 and histone deacetylases (predicted in silico). An algorithm combining CLDN10, HMGA2, and LAMB3 transcripts was able to discriminate tumors from BTL samples (94% sensitivity and 96% specificity in validation set). High algorithm scores were associated with regional lymph node metastases. Conclusions: A promising tool with high performance for PTC diagnosis based on three transcripts was designed with the potential to predict lymph node metastasis risk.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)AC Camargo Canc Ctr, Int Res Ctr, BR-01509010 Sao Paulo, SP, BrazilSao Paulo State Univ, Fac Med, BR-18618970 Botucatu, SP, BrazilSao Paulo State Univ, Fac Med, BR-18618970 Botucatu, SP, BrazilFAPESP: 2008/57887-9CNPq: CNPq 573589/08-9FAPESP: 2010/09526-7FAPESP: 2010/18370-0Endocrine SocAC Camargo Canc CtrUniversidade Estadual Paulista (Unesp)Barros-Filho, Mateus CamargoMarchi, Fabio AlbuquerquePinto, Clovis AntonioRogatto, Silvia Regina [UNESP]Kowalski, Luiz Paulo2018-11-27T00:48:00Z2018-11-27T00:48:00Z2015-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleE890-E899application/pdfhttp://dx.doi.org/10.1210/jc.2014-4053Journal Of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 100, n. 6, p. E890-E899, 2015.0021-972Xhttp://hdl.handle.net/11449/16490010.1210/jc.2014-4053WOS:000360840000009WOS000360840000009.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Clinical Endocrinology & Metabolisminfo:eu-repo/semantics/openAccess2024-09-03T14:30:11Zoai:repositorio.unesp.br:11449/164900Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T14:30:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
title |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
spellingShingle |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma Barros-Filho, Mateus Camargo |
title_short |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
title_full |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
title_fullStr |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
title_full_unstemmed |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
title_sort |
High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma |
author |
Barros-Filho, Mateus Camargo |
author_facet |
Barros-Filho, Mateus Camargo Marchi, Fabio Albuquerque Pinto, Clovis Antonio Rogatto, Silvia Regina [UNESP] Kowalski, Luiz Paulo |
author_role |
author |
author2 |
Marchi, Fabio Albuquerque Pinto, Clovis Antonio Rogatto, Silvia Regina [UNESP] Kowalski, Luiz Paulo |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
AC Camargo Canc Ctr Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Barros-Filho, Mateus Camargo Marchi, Fabio Albuquerque Pinto, Clovis Antonio Rogatto, Silvia Regina [UNESP] Kowalski, Luiz Paulo |
description |
Context: Thyroid nodules are common in adult population and papillary thyroid carcinoma (PTC) is the most frequent malignant finding. The natural history of PTC remains poorly understood and current diagnostic methods limitations are responsible for a significant number of potentially avoidable surgeries. Objective: This study aimed to identify molecular markers to improve the diagnosis of thyroid lesions. Design: Gene expression profiling was performed using microarray in 61 PTC and 13 surrounding normal tissues (NT). A reliable gene list was established using cross-study validation (138 matched PTC/NT from external databases). Results were collectively interpreted by in silico analysis. A panel of 28 transcripts was evaluated by RT-qPCR, including benign thyroid lesions (BTL) and other follicular cell-derived thyroid carcinomas (OFDTC). Adiagnostic algorithm was developed (training set: 23 NT, 8 BTL, and 86 PTC), validated (independent set: 10 NT, 140 BTL, 120 PTC, and 12 OFDTC) and associated with clinical features. Results: GABRB2 was ranked as the most frequently up-regulated gene in PTC (cross-study validation). Altered genes in PTC suggested a loss of T-4 responsiveness and dysregulation of retinoic acid metabolism, highlighting the putative activation of EZH2 and histone deacetylases (predicted in silico). An algorithm combining CLDN10, HMGA2, and LAMB3 transcripts was able to discriminate tumors from BTL samples (94% sensitivity and 96% specificity in validation set). High algorithm scores were associated with regional lymph node metastases. Conclusions: A promising tool with high performance for PTC diagnosis based on three transcripts was designed with the potential to predict lymph node metastasis risk. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-06-01 2018-11-27T00:48:00Z 2018-11-27T00:48:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1210/jc.2014-4053 Journal Of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 100, n. 6, p. E890-E899, 2015. 0021-972X http://hdl.handle.net/11449/164900 10.1210/jc.2014-4053 WOS:000360840000009 WOS000360840000009.pdf |
url |
http://dx.doi.org/10.1210/jc.2014-4053 http://hdl.handle.net/11449/164900 |
identifier_str_mv |
Journal Of Clinical Endocrinology & Metabolism. Washington: Endocrine Soc, v. 100, n. 6, p. E890-E899, 2015. 0021-972X 10.1210/jc.2014-4053 WOS:000360840000009 WOS000360840000009.pdf |
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 |
E890-E899 application/pdf |
dc.publisher.none.fl_str_mv |
Endocrine Soc |
publisher.none.fl_str_mv |
Endocrine Soc |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021393567318016 |