Department of Endocrinology, Metabolism and Internal Diseases, Poznan University of Medical Sciences, 60-355 Poznań, Poland.
Department of Nuclear Medicine, University Hospital Marburg, 35043 Marburg, Germany.
Int J Mol Sci. 2019 Jun 26;20(13):3126. doi: 10.3390/ijms20133126.
We aimed to identify differences in mutational status between follicular thyroid adenoma (FTA) and follicular thyroid cancer (FTC). The study included 35 patients with FTA and 35 with FTC. DNA was extracted from formalin-fixed paraffin-embedded (FFPE) samples from thyroidectomy. Next-generation sequencing (NGS) was performed with the 50-gene Ion AmpliSeq Cancer Hotspot Panel v2. Potentially pathogenic mutations were found in 14 (40%) FTA and 24 (69%) FTC patients (OR (95%CI) = 3.27 (1.22-8.75)). The number of mutations was higher in patients with FTC than FTA (-value = 0.03). and mutations were present only in patients with FTA, while defects in , , , , , , and were detected exclusively in FTC patients. mutations increased the risk of FTC; OR (95%CI) = 29.24 (1.64-522.00); -value = 0.001. -positivity was higher in FTC than in the FTA group (51.4% vs. 28.6%; -value = 0.051). The presence of and with no mutations increased FTC detectability by 17.1%, whereas the absence of and with a presence of mutations increased FTA detectability by 5.7%. and are candidate markers for detecting malignancy in follicular lesions. The best model to predict FTA and FTC may consist of , , and mutations considered together.
我们旨在确定滤泡状甲状腺腺瘤(FTA)和滤泡状甲状腺癌(FTC)之间的突变状态差异。该研究纳入了 35 例 FTA 和 35 例 FTC 患者。从甲状腺切除术的福尔马林固定石蜡包埋(FFPE)样本中提取 DNA。采用 50 基因 Ion AmpliSeq Cancer Hotspot Panel v2 进行下一代测序(NGS)。在 14 例(40%)FTA 和 24 例(69%)FTC 患者中发现了潜在致病性突变(OR(95%CI)=3.27(1.22-8.75))。与 FTA 相比,FTC 患者的突变数量更高(-值=0.03)。和 突变仅存在于 FTA 患者中,而在 FTC 患者中仅检测到 、 、 、 、 、 和 缺陷。 突变增加 FTC 的风险;OR(95%CI)=29.24(1.64-522.00);-值=0.001。FTC 组的 阳性率高于 FTA 组(51.4% vs. 28.6%;-值=0.051)。不存在 且存在 突变可使 FTC 的检出率提高 17.1%,而不存在 且存在 突变可使 FTA 的检出率提高 5.7%。和 是检测滤泡性病变恶性肿瘤的候选标志物。预测 FTA 和 FTC 的最佳模型可能由 、 、 和 突变共同组成。