Contribution of the BRAF oncogene in the pre-operative phase of thyroid carcinoma

Numerous experiments have been conducted over the last few years aiming to identify molecular markers that show the diagnostic accuracy of fine-needle aspiration (FNA), particularly in thyroid lesions that are considered indeterminate. Using certain search arguments and previously defined criteria,...

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Veröffentlicht in:Oncology letters 2013-07, Vol.6 (1), p.191-196
Hauptverfasser: RODRIGUES, HOMERO GUSTAVO CORREIA, DE PONTES, ALANA ABRANTES NOGUEIRA, ADAN, LUIS FERNANDO
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container_title Oncology letters
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creator RODRIGUES, HOMERO GUSTAVO CORREIA
DE PONTES, ALANA ABRANTES NOGUEIRA
ADAN, LUIS FERNANDO
description Numerous experiments have been conducted over the last few years aiming to identify molecular markers that show the diagnostic accuracy of fine-needle aspiration (FNA), particularly in thyroid lesions that are considered indeterminate. Using certain search arguments and previously defined criteria, 37 studies reporting experiments with the BRAF mutation in pre-operative FNA of the thyroid were selected from the electronic databases PUBMED, MEDLINE, SCOPUS and LILACS, in order to gather evidence with regard to the possible contribution of BRAF in the management of thyroid carcinoma. There were no cases positive for BRAF in follicular carcinomas (FTCs), Hürthle cell carcinomas (HCCs) or medullary thyroid carcinomas (MTCs). Among the 11 cases of anaplastic thyroid carcinomas (ATC), three showed positive results for the BRAF mutation. The number of cases positive for BRAF among the benign lesions was not significant. The average prevalence of BRAF-positive cases in papillary carcinomas (PTC) was 58.6%, while in follicular variants of papillary carcinoma (FVPTC), the average prevalence was 29.6%. For lesions diagnosed as indeterminate or suspicious, the average prevalence of BRAF positivity in PTC was 48.5%. The experiments included in the present study indicated a specificity of almost 100% and a high predominance of the BRAF mutation in PTC, distinguishing the marker in the planning and medical management of papillary carcinoma of the thyroid.
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The experiments included in the present study indicated a specificity of almost 100% and a high predominance of the BRAF mutation in PTC, distinguishing the marker in the planning and medical management of papillary carcinoma of the thyroid.</description><subject>Age</subject><subject>BRAF mutation</subject><subject>Experiments</subject><subject>fine-needle aspiration</subject><subject>Gender</subject><subject>Hospital costs</subject><subject>Mutation</subject><subject>Oncology</subject><subject>papillary thyroid carcinoma</subject><subject>Proteins</subject><subject>Studies</subject><subject>Surgery</subject><subject>Thyroid cancer</subject><issn>1792-1074</issn><issn>1792-1082</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkd1LHDEUxUOpVFHffC4DQulDZ5ubTGaSl8J20VYQpKLPIZvJupHZ3GkyI_jfm_3oVg2BfNxfDvfkEHIGdMKlYt-xmzAKfAJcqA_kCBrFSqCSfdzvm-qQnKb0SPMQNUhZfyKHjKuqlpQdkT8zDEP083HwGApcFMPSFT9vp5cFBosPLrjCh81lH12JvYtm8E_5tDTJbfnniL4trInWB1yZE3KwMF1yp7v1mNxfXtzNfpfXN7-uZtPr0lYVH0porLJCNcrNBae1FKwRglmmuHOtBdZKMLYyrZE0F6QF7hYAopFzYLRVgh-TH1vdfpyv8hOXfZhO99GvTHzWaLx-Wwl-qR_wSfOmYjWvssDXnUDEv6NLg175ZF3XmeBwTBokq0VurFIZPX-HPuIYQ7anQXGWv7XZUN-2lI2YUnSLfTNA9ToujZ1ex6XXcWX882sDe_hfOBn4sgVSb0LrW0z_3XUlrUsKeSrgL_tUm8g</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>RODRIGUES, HOMERO GUSTAVO CORREIA</creator><creator>DE PONTES, ALANA ABRANTES NOGUEIRA</creator><creator>ADAN, LUIS FERNANDO</creator><general>D.A. 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source Spandidos Publications Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Age
BRAF mutation
Experiments
fine-needle aspiration
Gender
Hospital costs
Mutation
Oncology
papillary thyroid carcinoma
Proteins
Studies
Surgery
Thyroid cancer
title Contribution of the BRAF oncogene in the pre-operative phase of thyroid carcinoma
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