Özdirik Burcin, Stueven Anna, Knorr Jana, Geisler Lukas, Mohr Raphael, Demir Münevver, Hellberg Teresa, Loosen Sven H, Benz Fabian, Wiedenmann Bertram, Tacke Frank, Wree Alexander, Jann Henning, Roderburg Christoph
Department of Hepatology and Gastroenterology, Campus Virchow Klinikum and Campus Charité Mitte, Charité University Medicine Berlin, 13353 Berlin, Germany.
Department of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074 Aachen, Germany.
J Clin Med. 2020 May 31;9(6):1647. doi: 10.3390/jcm9061647.
Neuroendocrine neoplasia (NEN) comprises heterogeneous tumors that are challenging to diagnose and, especially in cases of poorly differentiated (G3) NEN, are associated with very limited survival. Novel biomarkers allowing an early diagnosis as well as an optimal selection of suitable treatment options are urgently needed to improve the outcome of these patients. Recently, alterations of soluble urokinase-type plasminogen activator receptor (suPAR) serum levels were described in various types of cancers. However, the role of circulating suPAR as a biomarker in patients with NEN is unknown. In this study, we measured suPAR serum levels in a large and well-characterized cohort of 187 patients with NEN (neuroendocrine carcinomas (NEC) = 30; neuroendocrine tumors (NET), = 157) as well as 44 healthy controls. suPAR concentrations were significantly elevated in patients compared to controls. However, suPAR concentrations were independent of tumor-related factors such as the proliferation activity according to Ki-67, tumor grading, TNM (TNM classification of malignant tumors) stage, somatostatin receptor expression or clinical features such as functional or nonfunctional disease and the presence of tumor relapse. Interestingly, suPAR concentrations in NET patients were similar when compared to those measured in NEC patients. In contrast to previous results from other malignancies, in our analysis suPAR levels were not a significant predictor of overall survival. In conclusion, our data suggests that suPAR serum concentrations are elevated in NEN patients but do not allow prediction of outcome.
神经内分泌肿瘤(NEN)由异质性肿瘤组成,诊断具有挑战性,尤其是在低分化(G3)NEN病例中,其生存期非常有限。迫切需要新的生物标志物以实现早期诊断并优化合适治疗方案的选择,从而改善这些患者的预后。最近,可溶性尿激酶型纤溶酶原激活物受体(suPAR)血清水平的改变在多种癌症类型中被描述。然而,循环suPAR作为NEN患者生物标志物的作用尚不清楚。在本研究中,我们检测了187例NEN患者(神经内分泌癌(NEC)=30例;神经内分泌肿瘤(NET)=157例)以及44名健康对照者的suPAR血清水平,该队列规模大且特征明确。与对照组相比,患者的suPAR浓度显著升高。然而,suPAR浓度与肿瘤相关因素无关,如根据Ki-67的增殖活性、肿瘤分级、TNM(恶性肿瘤TNM分类)分期、生长抑素受体表达,或与功能或无功能疾病以及肿瘤复发情况等临床特征无关。有趣的是,NET患者的suPAR浓度与NEC患者测得的浓度相似。与其他恶性肿瘤先前的结果相反,在我们的分析中,suPAR水平不是总生存期的显著预测指标。总之,我们的数据表明NEN患者的suPAR血清浓度升高,但无法预测预后。