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In Japanese patients with papillary thyroid carcinoma, TERT promoter mutation is associated with poor prognosis, in contrast to BRAF (V600E) mutation

机译:与BRAF(V600E)突变相反,在日本甲状腺乳头状癌患者中,TERT启动子突变与预后不良相关

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The prognostic value of BRAF (V600E) and TERT promoter mutation in papillary thyroid carcinoma (PTC) is controversial. We examined alterations in BRAF (V600E) and TERT promoter by PCR-direct sequencing in PTC of 144 Japanese patients. Alternative lengthening of telomeres was examined as another mechanism of telomere maintenance by immunohistochemical staining for ATRX and DAXX. Of the clinicopathological characteristics, regional lymph node metastasis, extra-thyroid extension, multifocality/intrathyroidal spread, and advanced stage (III/V) were associated with shorter disease-free survival rate (DFSR). TERT promoter mutation was found in eight patients (6 %), and this was significantly associated with total thyroidectomy, multifocality/intrathyroidal spread, lymph node metastasis and advanced stage. The BRAF (V600E) mutation was found in 53 patients (38.2 %) but was not associated with any clinicopathological factors. TERT mutations were not correlated with BRAF (V600E) mutation status. TERT mutation-positive tumors (TERT+) showed lower DFSR than BRAF (V600E) -mutation-positive tumors (BRAF (V600E) +), and TERT+/BRAF (V600E) + tumors showed lower DFSR than BRAF (V600E) + tumors. No cases showed loss of ATRX/DAXX expression by immunohistochemistry. TERT promoter mutations showed a lower prevalence in our series and appeared to be associated with aggressive behavior. In PTCs, telomerase activation by TERT promoter mutation might be more important than alternative lengthening of telomeres.
机译:BRAF(V600E)和TERT启动子突变在甲状腺乳头状癌(PTC)中的预后价值存在争议。我们通过PCR直接测序在144例日本患者中检查了BRAF(V600E)和TERT启动子的变化。通过对ATRX和DAXX进行免疫组织化学染色,检查端粒的替代性延长是端粒维持的另一种机制。在临床病理特征中,区域淋巴结转移,甲状腺外扩展,多灶性/甲状腺内扩散和晚期(III / V)与较短的无病生存期(DFSR)相关。在8例患者(6%)中发现了TERT启动子突变,这与全甲状腺切除术,多灶性/甲状腺内扩散,淋巴结转移和晚期显着相关。在53例患者(38.2%)中发现了BRAF(V600E)突变,但与任何临床病理因素无关。 TERT突变与BRAF(V600E)突变状态无关。 TERT突变阳性肿瘤(TERT +)的DFSR低于BRAF(V600E)-突变阳性肿瘤(BRAF(V600E)+),而TERT + / BRAF(V600E)+肿瘤的DFSR低于BRAF(V600E)+肿瘤。没有病例显示免疫组织化学检测到ATRX / DAXX表达丢失。 TERT启动子突变在我们的系列中显示出较低的流行率,并且似乎与攻击行为有关。在PTC中,通过TERT启动子突变激活端粒酶可能比端粒的替代延长更为重要。

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