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微 RNA 表达谱有助于从细针抽吸细胞中区分良性结节和甲状腺乳头状癌。

MicroRNA expression profile helps to distinguish benign nodules from papillary thyroid carcinomas starting from cells of fine-needle aspiration.

机构信息

Department of Endocrinology, Research Center of Excellence AmbiSEN, University of Pisa, Via Paradisa 2, 56124 Pisa, Italy.

出版信息

Eur J Endocrinol. 2012 Sep;167(3):393-400. doi: 10.1530/EJE-12-0400. Epub 2012 Jun 22.

DOI:10.1530/EJE-12-0400
PMID:22728346
Abstract

OBJECTIVE

MicroRNAs (miRNAs) are small endogenous noncoding RNAs that pair with target messengers regulating gene expression. Changes in miRNA levels occur in thyroid cancer. Fine-needle aspiration (FNA) with cytological evaluation is the most reliable tool for malignancy prediction in thyroid nodules, but cytological diagnosis remains undetermined for 20% of nodules.

DESIGN

In this study, we evaluated the expression of seven miRNAs in benign nodules, papillary thyroid carcinomas (PTCs), and undetermined nodules at FNA.

METHODS

The prospective study included 141 samples obtained by FNA of thyroid nodules from 138 patients. miRNA expression was evaluated by quantitative RT-PCR and statistical analysis of data was performed. Genetic analysis of codon 600 of BRAF gene was also performed.

RESULTS

Using data mining techniques, we obtained a criterion to classify a nodule as benign or malignant on the basis of miRNA expression. The decision model based on the expression of miR-146b, miR-155, and miR-221 was valid for 86/88 nodules with determined cytology (97.73%), and adopting cross-validation techniques we obtained a reliability of 78.41%. The prediction was valid for 31/53 undetermined nodules with 16 false-positive and six false-negative predictions. The mutated form V600E of BRAF gene was demonstrated in 19/43 PTCs and in 1/53 undetermined nodules.

CONCLUSIONS

The expression profiles of three miRNAs allowed us to distinguish benign from PTC starting from FNA. When the assay was applied to discriminate thyroid nodules with undetermined cytology, a low sensitivity and specificity despite the low number of false-negative predictions was obtained, limiting the practical interest of the method.

摘要

目的

微小 RNA(miRNA)是与靶信使 RNA 配对的小型内源性非编码 RNA,调节基因表达。miRNA 水平的变化发生在甲状腺癌中。细针抽吸(FNA)和细胞学评估是预测甲状腺结节恶性肿瘤最可靠的工具,但细胞学诊断对 20%的结节仍不确定。

设计

在这项研究中,我们评估了 7 种 miRNA 在良性结节、甲状腺乳头状癌(PTC)和 FNA 不确定结节中的表达。

方法

这项前瞻性研究包括了 138 例患者的 141 个甲状腺结节的 FNA 样本。通过定量 RT-PCR 评估 miRNA 表达,并对数据进行了统计分析。还对 BRAF 基因第 600 位密码子的遗传分析。

结果

使用数据挖掘技术,我们获得了一种基于 miRNA 表达来分类结节良性或恶性的标准。基于 miR-146b、miR-155 和 miR-221 表达的决策模型对 88 个确定细胞学的结节(97.73%)有效,采用交叉验证技术,我们获得了 78.41%的可靠性。对 53 个不确定的结节进行预测,有 16 个假阳性和 6 个假阴性预测。BRAF 基因的 V600E 突变形式在 43 个 PTC 中和 1 个不确定的结节中被证明存在。

结论

从 FNA 开始,三种 miRNA 的表达谱可区分良性和 PTC。当该检测方法应用于鉴别不确定细胞学的甲状腺结节时,尽管假阴性预测较少,但获得的敏感性和特异性较低,限制了该方法的实际意义。

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