PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression

Detalhes bibliográficos
Autor(a) principal: Cerutti, Janete Maria [UNIFESP]
Data de Publicação: 2011
Outros Autores: Oler, Gisele [UNIFESP], Delcelo, Rosana [UNIFESP], Gerardt, Rene, Michaluart, Pedro, Souza, Sandro J. de, Galante, Pedro A. F., Huang, Peng, Riggins, Gregory J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
dARK ID: ark:/48912/0013000013grg
DOI: 10.1210/jc.2010-1318
Texto Completo: http://dx.doi.org/10.1210/jc.2010-1318
http://repositorio.unifesp.br/handle/11600/33218
Resumo: Context: A better means to accurately identify malignant thyroid nodules and to distinguish them from benign tumors is needed. We previously identified markers for detecting thyroid malignancy, with sensitivity estimated at or close to 100%. One lingering problem with these markers was that false positives occurred with Hurthle cell adenomas (HCA) which lowered test specificity.Methods: To locate accurate diagnostic markers, we profiled in depth the transcripts of a HCA and a Hurthle cell carcinoma (HCC). From 1146 differentially expressed genes, 18 transcripts specifically expressed in HCA were tested by quantitative PCR in a wide range of thyroid tumors (n = 76). Sensibility and specificity were calculated using receiver operating characteristic (ROC). Selected markers were further validated in an independent set of thyroid tumors (n = 82) by immunohistochemistry. To define the panel that would yield best diagnostic accuracy, these markers were tested in combination with our previous identified markers.Results: Seventeen of the 18 genes showed statistical significance based on a mean relative level of expression (P < 0.05). KLK1 (sensitivity = 0.97) and PVALB (sensitivity = 0.94) were the best candidate markers. the combination of PVALB and C1orf24 increased specificity to > 97% and maintained sensitivity for detection of carcinoma.Conclusion: We identified tumor markers that can be used in combination for a more accurate preoperative diagnosis of thyroid nodules and for postoperative diagnosis of thyroid carcinoma in tumor sections. This improved test would help physicians rapidly focus treatment on true malignancies and avoid unnecessary treatment of benign tumors, simultaneously improving medical care and reducing costs. (J Clin Endocrinol Metab 96: E151-E160, 2011)
id UFSP_8ddec7a67d8d4f11d127ab993baf35d2
oai_identifier_str oai:repositorio.unifesp.br/:11600/33218
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene ExpressionContext: A better means to accurately identify malignant thyroid nodules and to distinguish them from benign tumors is needed. We previously identified markers for detecting thyroid malignancy, with sensitivity estimated at or close to 100%. One lingering problem with these markers was that false positives occurred with Hurthle cell adenomas (HCA) which lowered test specificity.Methods: To locate accurate diagnostic markers, we profiled in depth the transcripts of a HCA and a Hurthle cell carcinoma (HCC). From 1146 differentially expressed genes, 18 transcripts specifically expressed in HCA were tested by quantitative PCR in a wide range of thyroid tumors (n = 76). Sensibility and specificity were calculated using receiver operating characteristic (ROC). Selected markers were further validated in an independent set of thyroid tumors (n = 82) by immunohistochemistry. To define the panel that would yield best diagnostic accuracy, these markers were tested in combination with our previous identified markers.Results: Seventeen of the 18 genes showed statistical significance based on a mean relative level of expression (P < 0.05). KLK1 (sensitivity = 0.97) and PVALB (sensitivity = 0.94) were the best candidate markers. the combination of PVALB and C1orf24 increased specificity to > 97% and maintained sensitivity for detection of carcinoma.Conclusion: We identified tumor markers that can be used in combination for a more accurate preoperative diagnosis of thyroid nodules and for postoperative diagnosis of thyroid carcinoma in tumor sections. This improved test would help physicians rapidly focus treatment on true malignancies and avoid unnecessary treatment of benign tumors, simultaneously improving medical care and reducing costs. (J Clin Endocrinol Metab 96: E151-E160, 2011)Universidade Federal de São Paulo, Genet Bases Thyroid Tumor Lab, BR-04039032 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pathol, BR-04039032 São Paulo, BrazilUniv São Paulo, Dept Pathol, BR-04039032 São Paulo, BrazilUniv São Paulo, Dept Surg, BR-04039032 São Paulo, BrazilLudwig Inst Canc Res, Lab Computat Biol, São Paulo Branch, BR-01323903 São Paulo, BrazilJohns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21231 USAUniversidade Federal de São Paulo, Genet Bases Thyroid Tumor Lab, BR-04039032 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Pathol, BR-04039032 São Paulo, BrazilWeb of ScienceNational Institutes of HealthFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)National Institutes of Health: CA113461FAPESP: 05/60330-8Endocrine SocUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Ludwig Inst Canc ResJohns Hopkins UnivCerutti, Janete Maria [UNIFESP]Oler, Gisele [UNIFESP]Delcelo, Rosana [UNIFESP]Gerardt, ReneMichaluart, PedroSouza, Sandro J. deGalante, Pedro A. F.Huang, PengRiggins, Gregory J.2016-01-24T14:05:53Z2016-01-24T14:05:53Z2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionE151-E160http://dx.doi.org/10.1210/jc.2010-1318Journal of Clinical Endocrinology & Metabolism. Chevy Chase: Endocrine Soc, v. 96, n. 1, p. E151-E160, 2011.10.1210/jc.2010-13180021-972Xhttp://repositorio.unifesp.br/handle/11600/33218WOS:000288185400022ark:/48912/0013000013grgengJournal of Clinical Endocrinology & Metabolisminfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T12:05:53Zoai:repositorio.unifesp.br/:11600/33218Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:53:39.097189Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
title PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
spellingShingle PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
Cerutti, Janete Maria [UNIFESP]
Cerutti, Janete Maria [UNIFESP]
title_short PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
title_full PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
title_fullStr PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
title_full_unstemmed PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
title_sort PVALB, a New Hurthle Adenoma Diagnostic Marker Identified through Gene Expression
author Cerutti, Janete Maria [UNIFESP]
author_facet Cerutti, Janete Maria [UNIFESP]
Cerutti, Janete Maria [UNIFESP]
Oler, Gisele [UNIFESP]
Delcelo, Rosana [UNIFESP]
Gerardt, Rene
Michaluart, Pedro
Souza, Sandro J. de
Galante, Pedro A. F.
Huang, Peng
Riggins, Gregory J.
Oler, Gisele [UNIFESP]
Delcelo, Rosana [UNIFESP]
Gerardt, Rene
Michaluart, Pedro
Souza, Sandro J. de
Galante, Pedro A. F.
Huang, Peng
Riggins, Gregory J.
author_role author
author2 Oler, Gisele [UNIFESP]
Delcelo, Rosana [UNIFESP]
Gerardt, Rene
Michaluart, Pedro
Souza, Sandro J. de
Galante, Pedro A. F.
Huang, Peng
Riggins, Gregory J.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Ludwig Inst Canc Res
Johns Hopkins Univ
dc.contributor.author.fl_str_mv Cerutti, Janete Maria [UNIFESP]
Oler, Gisele [UNIFESP]
Delcelo, Rosana [UNIFESP]
Gerardt, Rene
Michaluart, Pedro
Souza, Sandro J. de
Galante, Pedro A. F.
Huang, Peng
Riggins, Gregory J.
description Context: A better means to accurately identify malignant thyroid nodules and to distinguish them from benign tumors is needed. We previously identified markers for detecting thyroid malignancy, with sensitivity estimated at or close to 100%. One lingering problem with these markers was that false positives occurred with Hurthle cell adenomas (HCA) which lowered test specificity.Methods: To locate accurate diagnostic markers, we profiled in depth the transcripts of a HCA and a Hurthle cell carcinoma (HCC). From 1146 differentially expressed genes, 18 transcripts specifically expressed in HCA were tested by quantitative PCR in a wide range of thyroid tumors (n = 76). Sensibility and specificity were calculated using receiver operating characteristic (ROC). Selected markers were further validated in an independent set of thyroid tumors (n = 82) by immunohistochemistry. To define the panel that would yield best diagnostic accuracy, these markers were tested in combination with our previous identified markers.Results: Seventeen of the 18 genes showed statistical significance based on a mean relative level of expression (P < 0.05). KLK1 (sensitivity = 0.97) and PVALB (sensitivity = 0.94) were the best candidate markers. the combination of PVALB and C1orf24 increased specificity to > 97% and maintained sensitivity for detection of carcinoma.Conclusion: We identified tumor markers that can be used in combination for a more accurate preoperative diagnosis of thyroid nodules and for postoperative diagnosis of thyroid carcinoma in tumor sections. This improved test would help physicians rapidly focus treatment on true malignancies and avoid unnecessary treatment of benign tumors, simultaneously improving medical care and reducing costs. (J Clin Endocrinol Metab 96: E151-E160, 2011)
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01
2016-01-24T14:05:53Z
2016-01-24T14:05:53Z
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 http://dx.doi.org/10.1210/jc.2010-1318
Journal of Clinical Endocrinology & Metabolism. Chevy Chase: Endocrine Soc, v. 96, n. 1, p. E151-E160, 2011.
10.1210/jc.2010-1318
0021-972X
http://repositorio.unifesp.br/handle/11600/33218
WOS:000288185400022
dc.identifier.dark.fl_str_mv ark:/48912/0013000013grg
url http://dx.doi.org/10.1210/jc.2010-1318
http://repositorio.unifesp.br/handle/11600/33218
identifier_str_mv Journal of Clinical Endocrinology & Metabolism. Chevy Chase: Endocrine Soc, v. 96, n. 1, p. E151-E160, 2011.
10.1210/jc.2010-1318
0021-972X
WOS:000288185400022
ark:/48912/0013000013grg
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 E151-E160
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_ 1822252113046011904
dc.identifier.doi.none.fl_str_mv 10.1210/jc.2010-1318