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Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer

BACKGROUND: BRAF is the most frequently mutated gene in differentiated thyroid cancer (DTC). Previous studies on DTC have well documented high rates of the BRAF(V600E) mutation in patients of mixed ages. Previous studies either included a mix of pediatric and adult patients or pediatric patients onl...

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Autores principales: Murugan, Avaniyapuram Kannan, Qasem, Ebtesam, Al-Hindi, Hindi, Shi, Yufei, Alzahrani, Ali S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936197/
https://www.ncbi.nlm.nih.gov/pubmed/27387551
http://dx.doi.org/10.1186/s12967-016-0958-x
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author Murugan, Avaniyapuram Kannan
Qasem, Ebtesam
Al-Hindi, Hindi
Shi, Yufei
Alzahrani, Ali S.
author_facet Murugan, Avaniyapuram Kannan
Qasem, Ebtesam
Al-Hindi, Hindi
Shi, Yufei
Alzahrani, Ali S.
author_sort Murugan, Avaniyapuram Kannan
collection PubMed
description BACKGROUND: BRAF is the most frequently mutated gene in differentiated thyroid cancer (DTC). Previous studies on DTC have well documented high rates of the BRAF(V600E) mutation in patients of mixed ages. Previous studies either included a mix of pediatric and adult patients or pediatric patients only. However, the prevalence of hotspot and non-hotspot BRAF mutations and its significance in pure adult DTCs is not yet well determined. In this study we determine the frequency of this classical BRAF mutation and other rare BRAF mutations in pure adult DTCs. METHODS: A total of 204 adult DTC samples (Age >18 years) were analyzed for mutations in exon 15 of the BRAF gene by performing polymerase chain reaction (PCR) amplification of tumor genomic DNAs and direct sequencing of amplicons using Sanger sequencing. Obtained results were correlated to clinical and pathological characteristics of DTCs. Statistical analyses were performed using SPSS (The Statistical Package for Social Sciences) version 20 software. RESULTS: Overall, BRAF mutations were identified in 48.5 % (99/204) of adult DTCs. Three rare non-hotspot mutations (T599I, T599dup and K601E) were detected in four tumor samples (2 %). One (K601E) of these non-hotspot mutations occurred in conventional papillary thyroid cancer (CPTC) and other three (T599I, T599dup and K601E) were found in follicular variant PTC. We found significant association between BRAF(V600E) mutation and age (P < 0.0001), extrathyroidal invasion (P = 0.017), lymph node metastasis (P = 0.038) and TNM stage III/IV (P = 0.001). CONCLUSIONS: Our study is the first to report BRAF mutations in a pure adult sample of DTCs of Saudi Arabian ethnicity. Our results show a high rate and a strong prognostic role of the classical BRAF(V600E) mutation and also suggest a common occurrence of non-hot spot mutations in adult DTC from this highly inbred population.
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spelling pubmed-49361972016-07-07 Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer Murugan, Avaniyapuram Kannan Qasem, Ebtesam Al-Hindi, Hindi Shi, Yufei Alzahrani, Ali S. J Transl Med Research BACKGROUND: BRAF is the most frequently mutated gene in differentiated thyroid cancer (DTC). Previous studies on DTC have well documented high rates of the BRAF(V600E) mutation in patients of mixed ages. Previous studies either included a mix of pediatric and adult patients or pediatric patients only. However, the prevalence of hotspot and non-hotspot BRAF mutations and its significance in pure adult DTCs is not yet well determined. In this study we determine the frequency of this classical BRAF mutation and other rare BRAF mutations in pure adult DTCs. METHODS: A total of 204 adult DTC samples (Age >18 years) were analyzed for mutations in exon 15 of the BRAF gene by performing polymerase chain reaction (PCR) amplification of tumor genomic DNAs and direct sequencing of amplicons using Sanger sequencing. Obtained results were correlated to clinical and pathological characteristics of DTCs. Statistical analyses were performed using SPSS (The Statistical Package for Social Sciences) version 20 software. RESULTS: Overall, BRAF mutations were identified in 48.5 % (99/204) of adult DTCs. Three rare non-hotspot mutations (T599I, T599dup and K601E) were detected in four tumor samples (2 %). One (K601E) of these non-hotspot mutations occurred in conventional papillary thyroid cancer (CPTC) and other three (T599I, T599dup and K601E) were found in follicular variant PTC. We found significant association between BRAF(V600E) mutation and age (P < 0.0001), extrathyroidal invasion (P = 0.017), lymph node metastasis (P = 0.038) and TNM stage III/IV (P = 0.001). CONCLUSIONS: Our study is the first to report BRAF mutations in a pure adult sample of DTCs of Saudi Arabian ethnicity. Our results show a high rate and a strong prognostic role of the classical BRAF(V600E) mutation and also suggest a common occurrence of non-hot spot mutations in adult DTC from this highly inbred population. BioMed Central 2016-07-07 /pmc/articles/PMC4936197/ /pubmed/27387551 http://dx.doi.org/10.1186/s12967-016-0958-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Murugan, Avaniyapuram Kannan
Qasem, Ebtesam
Al-Hindi, Hindi
Shi, Yufei
Alzahrani, Ali S.
Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title_full Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title_fullStr Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title_full_unstemmed Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title_short Classical V600E and other non-hotspot BRAF mutations in adult differentiated thyroid cancer
title_sort classical v600e and other non-hotspot braf mutations in adult differentiated thyroid cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936197/
https://www.ncbi.nlm.nih.gov/pubmed/27387551
http://dx.doi.org/10.1186/s12967-016-0958-x
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