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利用超声引导下细针穿刺活检样本的蛋白质组学分析破译甲状腺乳头状微癌淋巴结转移的新型生物标志物。

Deciphering novel biomarkers of lymph node metastasis of thyroid papillary microcarcinoma using proteomic analysis of ultrasound-guided fine-needle aspiration biopsy samples.

机构信息

Department of Endocrine, Qilu Hospital, Shandong University, Ji'nan 250012, Shandong, PR China.

Hospital for Reproductive Medicine Affiliated to Shandong University, Ji'nan 250012, Shandong, PR China.

出版信息

J Proteomics. 2019 Jul 30;204:103414. doi: 10.1016/j.jprot.2019.103414. Epub 2019 Jun 10.

DOI:10.1016/j.jprot.2019.103414
PMID:31195151
Abstract

Thyroid papillary microcarcinoma is now a common clinical problem. Cervical lymph node metastasis is the main metastasis mode of PTMC. However, before operation, it is still difficult to determine exactly whether PTMC patient is suffering with cervical lymph node metastasis. To resolve this dilemma, for better selection of optimum treatment plans, it is necessary to investigate the overall changes in proteomes of PTMC, and evaluate the potential of biomarkers to predict lymph node metastasis. Tandem mass tags combined with multidimensional liquid chromatography and mass spectrometry analyses were used aiming to screen the proteomic profiles of fine-needle aspiration biopsy samples. Quantitative proteomic analysis, significant pathway and functional categories were investigated. In total, 3391 proteins of the 3793 protein groups identified were quantified. Bioinformatics analysis indicated that differentially expressed proteins were involved in multiple biological functions, metastasis-related pathways. Moreover, IFN-stimulated gene 15 proteins were found to be well distinguished between patients with lymph node metastatic and patients with nonmetastatic PTMC. Knocking down ISG15 with shRNA inhibited the xenografted tumor growth. This study provided a reference proteome map for lymph node metastatic PTMC. ISG15 probably is a prognosis marker of thyroid papillary microcarcinoma patients with lymph node metastasis. SIGNIFICANCE: Nowadays, thyroid cancer has become a widespread epidemic. The rate of thyroid cancer incidence has been faster than any other cancers, reported by the American Cancer Society. Papillary thyroid microcarcinoma (PTMC) is a subset of PTC defined as PTC measuring≤1 cm in size, which comprises nearly one-half of all the cases of PTCs. Actually, the rapidly increasing global incidence of PTC is mainly attributed to the corresponding increase in the diagnosis of PTMC. Scholars have figuratively compared the increase of PTMC to the "tsunami". The treatment scheme for PTMC is still not uniform, and the controversy is mainly focused on the necessity of surgery treatment. PTMCs often have an indolent course in the absence of evidence of metastatic cervical lymph nodes, distant metastases and extrathyroidal extension. Therefore, it is important for us to reliably differentiate the small number of PTMC patients developing significant metastases progression from the larger population of patients that harbor indolent PTMCs. The present study aimed to investigate the overall changes in proteomes of PTMC, and evaluate the potential of biomarkers to predict lymph node metastasis. Tandem mass tags (TMT) combined with multidimensional liquid chromatography and mass spectrometry analyses were used aiming to screen the proteomic profiles of fine-needle aspiration biopsy (FNAB) samples. Quantitative proteomic analysis, significant pathway and functional categories were investigated. Our results showed that some differential expression proteins were likely to be important resources for finding new diagnostic biomarkers.

摘要

甲状腺乳头状微癌现在是一个常见的临床问题。颈部淋巴结转移是 PTMC 的主要转移方式。然而,在手术前,仍然很难准确判断 PTMC 患者是否患有颈部淋巴结转移。为了解决这一困境,为了更好地选择最佳治疗方案,有必要研究 PTMC 的蛋白质组的整体变化,并评估生物标志物预测淋巴结转移的潜力。使用串联质量标签(TMT)结合多维液相色谱和质谱分析,旨在筛选细针抽吸活检(FNAB)样本的蛋白质组图谱。进行定量蛋白质组学分析,研究显著的途径和功能类别。总共鉴定了 3793 个蛋白质组中的 3391 个蛋白质被定量。生物信息学分析表明,差异表达蛋白参与了多种生物学功能和转移相关途径。此外,发现 IFN 刺激基因 15 蛋白可很好地区分淋巴结转移性和非转移性 PTMC 患者。用 shRNA 敲低 ISG15 抑制了异种移植肿瘤的生长。这项研究为淋巴结转移性 PTMC 提供了参考蛋白质组图谱。ISG15 可能是甲状腺乳头状微癌患者淋巴结转移的预后标志物。意义:如今,甲状腺癌已成为一种广泛流行的疾病。据美国癌症协会报道,甲状腺癌的发病率增长速度比任何其他癌症都要快。甲状腺乳头状微癌(PTMC)是 PTC 的一个亚类,定义为 PTC 大小≤1cm,占 PTC 病例的近一半。实际上,全球 PTC 发病率的快速增长主要归因于 PTMC 诊断相应增加。学者们将 PTMC 的增加比喻为“海啸”。PTMC 的治疗方案仍不统一,争议主要集中在手术治疗的必要性上。PTMC 在没有证据表明颈部淋巴结转移、远处转移和甲状腺外延伸的情况下,往往具有惰性病程。因此,对于我们来说,可靠地区分少数发生显著转移进展的 PTMC 患者与较大比例的隐匿性 PTMC 患者是非常重要的。本研究旨在研究 PTMC 的蛋白质组的整体变化,并评估生物标志物预测淋巴结转移的潜力。使用串联质量标签(TMT)结合多维液相色谱和质谱分析,旨在筛选细针抽吸活检(FNAB)样本的蛋白质组图谱。进行定量蛋白质组学分析,研究显著的途径和功能类别。我们的研究结果表明,一些差异表达蛋白可能是寻找新的诊断生物标志物的重要资源。

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