Department of Medical Sciences, Section of Endocrine Oncology, Uppsala University, Rudbecklaboratoriet, hus R3, vån 2, Dag Hammarskjölds väg 20, 752 85, Uppsala, Sweden.
Department of Pathology, University of Bern, Bern, Switzerland.
Sci Rep. 2020 Jun 30;10(1):10639. doi: 10.1038/s41598-020-67670-7.
Pancreatic neuroendocrine neoplasms (PanNENs) are rare tumours that compose 1-2% of all pancreatic tumours. Patients with metastatic grade 3 neoplasia are usually treated with chemotherapy but have a poor progression-free and overall survival. According to the WHO 2017 classification, they are divided into neuroendocrine tumours (NETs) G3 and neuroendocrine carcinomas (NECs). Despite the new classification, new diagnostic and prognostic biomarkers are needed to sub-categorise the patients and to help guide therapy decisions. Blood from 42 patients and 42 healthy controls were screened for the presence of 92 proteins with the Immuno-Oncology panel using the Proximity Extension Assay provided by Olink Biosciences. Immunohistochemical staining of FAS ligand (FASLG) was performed on 16 patient tumour specimens using a commercial antibody. Fifty-four out of 87 evaluable proteins differed significantly in concentration between blood from patients and blood from healthy controls. FASLG was the only protein for which the concentration in blood was significantly lower in patients compared to controls and the levels correlated negatively to Ki-67 index. Seven of 14 evaluable PanNEN G3 specimens showed FASLG immunoreactivity in the tumour cells while there was scattered immunoreactivity in immune cells. Positive FASLG immunoreactivity correlated to well-differentiated morphology. FASLG concentration in blood was significantly lower in patients with pancreatic NENs G3 compared to controls, and the expression in tumour tissue was variable. Furthermore, FASLG was negatively correlated to Ki-67 and was more frequently expressed in well-differentiated tumours. Taken together, these results may suggest a role of FASLG in PanNENs.
胰腺神经内分泌肿瘤(PanNENs)是一种罕见的肿瘤,占所有胰腺肿瘤的 1-2%。转移性 3 级肿瘤患者通常接受化疗治疗,但无进展生存期和总生存期较差。根据 2017 年 WHO 分类,它们分为神经内分泌肿瘤(NETs)G3 和神经内分泌癌(NECs)。尽管有了新的分类,但仍需要新的诊断和预后生物标志物来对患者进行亚分类,并帮助指导治疗决策。使用 Olink Biosciences 提供的接近延伸分析(Proximity Extension Assay),通过免疫肿瘤学面板对 42 名患者和 42 名健康对照者的血液进行了 92 种蛋白质的检测。使用商业抗体对 16 例患者肿瘤标本进行了 FAS 配体(FASLG)的免疫组织化学染色。在可评估的 87 种蛋白质中,有 54 种在患者血液和健康对照者血液中的浓度有显著差异。FASLG 是唯一一种在患者血液中浓度明显低于对照者的蛋白质,其水平与 Ki-67 指数呈负相关。在可评估的 14 份 PanNEN G3 标本中,有 7 份肿瘤细胞中存在 FASLG 免疫反应性,而免疫细胞中存在散在的免疫反应性。阳性 FASLG 免疫反应性与分化良好的形态学相关。与对照组相比,G3 期胰腺神经内分泌肿瘤患者的血液中 FASLG 浓度显著降低,且肿瘤组织中的表达情况存在差异。此外,FASLG 与 Ki-67 呈负相关,且在分化较好的肿瘤中表达更为频繁。综上所述,这些结果可能提示 FASLG 在 PanNENs 中的作用。