Allele Percentage of the BRAF V600E Mutation in Papillary Thyroid Carcinomas and Corresponding Lymph Node Metastases: No Evidence for a Role in Tumor Progression
Context:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as...
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Published in | The journal of clinical endocrinology and metabolism Vol. 98; no. 5; pp. E934 - E942 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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United States
Oxford University Press
01.05.2013
Copyright by The Endocrine Society |
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Online Access | Get full text |
ISSN | 0021-972X 1945-7197 1945-7197 |
DOI | 10.1210/jc.2012-3930 |
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Abstract | Context:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy.Objective:We aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs.Study Design:The presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs.Results:No significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions.Conclusions:In this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs. |
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AbstractList | Context:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy.Objective:We aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs.Study Design:The presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs.Results:No significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions.Conclusions:In this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs. CONTEXT:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy. OBJECTIVE:We aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs. STUDY DESIGN:The presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs. RESULTS:No significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions. CONCLUSIONS:In this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs. The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy.CONTEXTThe relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy.We aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs.OBJECTIVEWe aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs.The presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs.STUDY DESIGNThe presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs.No significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions.RESULTSNo significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions.In this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs.CONCLUSIONSIn this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs. The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has been associated with several clinicopathological features, but the lack of consistency among data does not support its usefulness as marker of tumor aggressiveness and poorer outcome. Due to the genetic heterogeneity of the tumor, both the occurrence and the allele percentage of the BRAF mutation should be considered to unravel this controversy. We aimed to evaluate the impact of the BRAF V600E mutation occurrence and the allele percentage on the metastatic process in PTCs. The presence and allele percentage of the BRAF mutation were determined by pyrosequencing in 132 cases of well-differentiated PTCs with (n = 37) or without lymph node metastases (LNMs) (n = 95) and in 40 LNMs matched with 35 PTCs. No significant differences were observed in either the occurrence or the allele percentage of V600E mutation between the 2 groups of PTCs with or without LNMs. The LNMs were heterogeneous for the V600E mutation as the primary lesions. In this study, the occurrence and percentage of the BRAF V600E mutated allele was not preferentially associated with the development of metastases and the average mutated allele percentage decreased as the tumor progresses from the primary site to the lymph node metastatic sites. These observations support the need to reevaluate the role of the BRAF V600E mutation as a negative prognostic marker in PTCs. |
Author | Frasoldati, Andrea Piana, Simonetta Ragazzi, Moira Gandolfi, Greta Ciarrocchi, Alessia Torricelli, Federica Sancisi, Valentina |
AuthorAffiliation | Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), Department of Oncology, Pathology Unit (M.R., S.P.), Department of Oncology, and Endocrinology Unit (A.F.), Department of Surgery, Arcispedale S. Maria Nuova-Istituto di Ricovero e Cura a Carattere Scientifico, 42123 Reggio Emilia, Italy |
AuthorAffiliation_xml | – name: Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), Department of Oncology, Pathology Unit (M.R., S.P.), Department of Oncology, and Endocrinology Unit (A.F.), Department of Surgery, Arcispedale S. Maria Nuova-Istituto di Ricovero e Cura a Carattere Scientifico, 42123 Reggio Emilia, Italy |
Author_xml | – sequence: 1 givenname: Greta surname: Gandolfi fullname: Gandolfi, Greta organization: 1Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), 42123 Reggio Emilia, Italy – sequence: 2 givenname: Valentina surname: Sancisi fullname: Sancisi, Valentina organization: 1Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), 42123 Reggio Emilia, Italy – sequence: 3 givenname: Federica surname: Torricelli fullname: Torricelli, Federica organization: 1Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), 42123 Reggio Emilia, Italy – sequence: 4 givenname: Moira surname: Ragazzi fullname: Ragazzi, Moira organization: 2Department of Oncology, Pathology Unit (M.R., S.P.), 42123 Reggio Emilia, Italy – sequence: 5 givenname: Andrea surname: Frasoldati fullname: Frasoldati, Andrea organization: 3Department of Oncology, and Endocrinology Unit (A.F.), Department of Surgery, Arcispedale S. Maria Nuova-Istituto di Ricovero e Cura a Carattere Scientifico, 42123 Reggio Emilia, Italy – sequence: 6 givenname: Simonetta surname: Piana fullname: Piana, Simonetta organization: 2Department of Oncology, Pathology Unit (M.R., S.P.), 42123 Reggio Emilia, Italy – sequence: 7 givenname: Alessia surname: Ciarrocchi fullname: Ciarrocchi, Alessia email: Alessia.Ciarrocchi@asmn.re.it organization: 1Laboratory of Molecular Biology (G.G., V.S., F.T., A.C.), 42123 Reggio Emilia, Italy |
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Snippet | Context:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This... CONTEXT:The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This... The relevance of the BRAF V600E mutation in papillary thyroid carcinoma (PTC) as a negative prognostic factor is a subject of intense debate. This mutation has... |
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SubjectTerms | Adolescent Adult Aged Alleles Amino Acid Substitution Carcinoma - genetics Carcinoma - metabolism Carcinoma - pathology Carcinoma - physiopathology Carcinoma, Papillary - genetics Carcinoma, Papillary - metabolism Carcinoma, Papillary - physiopathology Carcinoma, Papillary - secondary Disease Progression DNA Mutational Analysis Exons Female Follow-Up Studies Gene Frequency Genetic Association Studies Humans Italy Lymph nodes Lymphatic Metastasis Lymphatic system Male Metastases Metastasis Middle Aged Mutation Papillary thyroid carcinoma Proto-Oncogene Proteins B-raf - chemistry Proto-Oncogene Proteins B-raf - genetics Proto-Oncogene Proteins B-raf - metabolism Thyroid Cancer, Papillary Thyroid gland Thyroid Neoplasms - genetics Thyroid Neoplasms - metabolism Thyroid Neoplasms - pathology Thyroid Neoplasms - physiopathology Tumors Young Adult |
Title | Allele Percentage of the BRAF V600E Mutation in Papillary Thyroid Carcinomas and Corresponding Lymph Node Metastases: No Evidence for a Role in Tumor Progression |
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