Abstract

BackgroundPapillary thyroid cancer is the most common endocrine malignancy. The most sensitive and specific diagnostic tool for thyroid nodule diagnosis is fine-needle aspiration (FNA) biopsy with cytological evaluation. Nevertheless, FNA biopsy is not always decisive leading to “indeterminate” or “suspicious” diagnoses in 10 %–30 % of cases. BRAF V600E detection is currently used as molecular test to improve the diagnosis of thyroid nodules, yet it lacks sensitivity. The aim of the present study was to identify novel molecular markers/computational models to improve the discrimination between benign and malignant thyroid lesions.MethodsWe collected 118 pre-operative thyroid FNA samples. All 118 FNA samples were characterized for the presence of the BRAF V600E mutation (exon15) by pyrosequencing and further assessed for mRNA expression of four genes (KIT, TC1, miR-222, miR-146b) by quantitative polymerase chain reaction. Computational models (Bayesian Neural Network Classifier, discriminant analysis) were built, and their ability to discriminate benign and malignant tumors were tested. Receiver operating characteristic (ROC) analysis was performed and principal component analysis was used for visualization purposes.ResultsIn total, 36/70 malignant samples carried the V600E mutation, while all 48 benign samples were wild type for BRAF exon15. The Bayesian neural network (BNN) and discriminant analysis, including the mRNA expression of the four genes (KIT, TC1, miR-222, miR-146b) showed a very strong predictive value (94.12 % and 92.16 %, respectively) in discriminating malignant from benign patients. The discriminant analysis showed a correct classification of 100 % of the samples in the malignant group, and 95 % by BNN. KIT and miR-146b showed the highest diagnostic accuracy of the ROC curve, with area under the curve values of 0.973 for KIT and 0.931 for miR-146b.ConclusionsThe four genes model proposed in this study proved to be highly discriminative of the malignant status compared with BRAF assessment alone. Its implementation in clinical practice can help in identifying malignant/benign nodules that would otherwise remain suspicious.Electronic supplementary materialThe online version of this article (doi:10.1186/s12885-015-1917-2) contains supplementary material, which is available to authorized users.

Highlights

  • Papillary thyroid cancer is the most common endocrine malignancy

  • It stills generates a percentage of suspicious papillary thyroid carcinoma (SPTC) and indeterminate follicular proliferation (IFP) diagnoses

  • Since the presence of BRAFV600E assures the malignancy of the thyroid nodule, whereas wild-type BRAF cannot determine a specific diagnosis by itself, we aimed at the evaluation, by quantitative polymerase chain reaction and a computational model, of the expression signature of four genes as a new genetic model to be added to the routine BRAF diagnostic test

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Summary

Introduction

Papillary thyroid cancer is the most common endocrine malignancy. The most sensitive and specific diagnostic tool for thyroid nodule diagnosis is fine-needle aspiration (FNA) biopsy with cytological evaluation. Since the presence of BRAFV600E assures the malignancy of the thyroid nodule, whereas wild-type BRAF cannot determine a specific diagnosis by itself, we aimed at the evaluation, by quantitative polymerase chain reaction (qPCR) and a computational model, of the expression signature of four genes as a new genetic model to be added to the routine BRAF diagnostic test. We propose this model when BRAF is wild-type in order to improve FNA diagnostic accuracy, especially for the nodules that would otherwise remain suspicious. Our four-gene model was characterized by a lower number of molecular markers compared with the previously developed models, resulting in more practical and usefulness at a clinical level

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