High Diagnostic Accuracy Based on CLDN10, HMGA2, and LAMB3 Transcripts in Papillary Thyroid Carcinoma

Detalhes bibliográficos
Autor(a) principal: Barros-Filho, Mateus Camargo
Data de Publicação: 2015
Outros Autores: Marchi, Fabio Albuquerque, Pinto, Clovis Antonio, Rogatto, Silvia Regina [UNESP], Kowalski, Luiz Paulo
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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spelling 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
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