Brain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Korea.
Departments of Internal Medicine, Open NBI Convergence Technology Research Laboratory, Yonsei University College of Medicine, Seoul, Korea.
Eur J Endocrinol. 2019 Aug;181(2):139-149. doi: 10.1530/EJE-18-1025.
Tumor location in papillary thyroid microcarcinoma (PTMC) might determine tumor outgrowth from the thyroid gland. However, the clinical implications of tumor location and minimal extrathyroid extension (mETE) have not been well elucidated. We aimed to investigate the relationship between tumor location and mETE to predict the aggressiveness of PTMC.
A total of 858 patients with PTMC were grouped according to tumor location on ultrasonography: central (cPTMC) and peripheral PTMC (pPTMC). PTMC without mETE (PTMC-mETE(-)) was divided further according to margin shape: encapsulated (E-) or infiltrative (I-). To understand the molecular biologic characteristics of PTMC presenting with an I-margin and mETE, transcriptome data from TCGA-THCA were analyzed using Gene Set Enrichment Analysis (GSEA).
pPTMC (n = 807, 94.1%) accounted for the majority of cases; mETE was identified only in pPTMC (403/807; 49.9%). pPTMC-mETE(+) showed aggressive clinical characteristics that increased the odds ratio (OR) for lymph node metastasis (LNM). Interestingly, subgroup analysis of PTMC-mETE(-) revealed that the I-margin also increased the OR for LNM, independent of other clinical factors. GSEA of TCGA-THCA data suggested coordinated upregulation of genes related to epithelial-mesenchymal transition (EMT) in PTC with mETE. Immunohistochemical staining for laminin subunit gamma 2 (LAMC2), CD59, E-cadherin and vimentin showed that these markers of EMT were associated with progressive changes in E-margin PTMC-mETE(-), I-margin PTMC-mETE(-) and pPTMC-mETE(+).
mETE related to peripheral location of PTMC is an important predictor of tumor invasiveness, as is the I-margin, which presents with EMT features similar to mETE. I-margin PTMC-mETE(-) and pPTMC-mETE(+) might reflect the pattern of invasive PTMC.
甲状腺乳头状微小癌(PTMC)的肿瘤位置可能决定肿瘤是否从甲状腺中生长出来。然而,肿瘤位置和最小甲状腺外扩展(mETE)的临床意义尚未得到很好的阐明。我们旨在研究肿瘤位置与 mETE 之间的关系,以预测 PTMC 的侵袭性。
根据超声检查的肿瘤位置,将 858 例 PTMC 患者分为中央型(cPTMC)和外周型(pPTMC)。无 mETE 的 PTMC(PTMC-mETE(-))进一步根据边缘形状分为包膜完整(E-)或浸润性(I-)。为了了解 mETE 为 I 型边缘的 PTMC 的分子生物学特征,使用基因集富集分析(GSEA)对 TCGA-THCA 的转录组数据进行分析。
pPTMC(n=807,94.1%)占多数;仅在 pPTMC 中发现 mETE(403/807;49.9%)。pPTMC-mETE(+) 表现出侵袭性临床特征,增加了淋巴结转移(LNM)的比值比(OR)。有趣的是,PTMC-mETE(-)的亚组分析表明,I 型边缘也增加了 LNM 的 OR,独立于其他临床因素。TCGA-THCA 数据的 GSEA 表明,伴有 mETE 的 PTC 中与上皮间质转化(EMT)相关的基因呈协同上调。免疫组织化学染色显示层粘连蛋白亚基γ2(LAMC2)、CD59、E-钙黏蛋白和波形蛋白这些 EMT 标志物与 E 型边缘 PTMC-mETE(-)、I 型边缘 PTMC-mETE(-)和 pPTMC-mETE(+)的进展性变化相关。
与 PTMC 外周位置相关的 mETE 是肿瘤侵袭性的重要预测因子,而 I 型边缘具有与 mETE 相似的 EMT 特征。I 型边缘 PTMC-mETE(-)和 pPTMC-mETE(+)可能反映了侵袭性 PTMC 的模式。