Department of Ophthalmology, Eberhard-Karls University Tuebingen, Schleichstr. 12-16, 72076 Tuebingen, Germany.
Graefes Arch Clin Exp Ophthalmol. 2012 Jun;250(6):887-95. doi: 10.1007/s00417-011-1786-6. Epub 2011 Sep 1.
About 50% of patients with uveal melanoma (UM) develop metastases during the course of their disease. We analyzed serum levels of Growth Differentiation Factor-15 (GDF-15), with the aim of identifying patients with early metastases.
GDF-15 concentration was measured using an enzyme-linked immunosorbent assay (ELISA) in serum samples from 188 UM patients (170 patients without metastases; 18 patients with clinically detectable metastases) and 18 healthy control individuals. Data were analyzed with respect to differences between patients with and without clinically detectable UM metastases. GDF-15 serum levels were further analyzed with regard to significant patient and tumor characteristics as revealed by histology and multiplex ligation-dependent probe amplification (MLPA) to determine chromosome 3 copy number. GDF-15 expression in UM was investigated by immunohistochemistry.
Patients with clinically detectable metastases had significantly higher GDF-15 serum levels compared to those without clinically detectable metastases as well as to healthy individuals (ANOVA; p < 0.001). GDF-15 concentrations in UM patients with overt clinically detectable metastases were significantly higher than those in UM patients with a second malignancy in remission but without clinically detected UM metastases (ANOVA; p < 0.001). No association between serum concentration of GDF-15 and clinical, pathological, and genetic features was observed. GDF-15 protein was only expressed in a minority of UM cells in most tumors.
Our data suggest that GDF-15 can be used as a serum marker for the diagnosis of metastases in UM patients. Further data collection and analysis are necessary to evaluate a possible prognostic role of GDF-15 in predicting early metastases.
约 50%的葡萄膜黑色素瘤(UM)患者在疾病过程中会发生转移。我们分析了生长分化因子 15(GDF-15)的血清水平,旨在确定具有早期转移的患者。
使用酶联免疫吸附试验(ELISA)测量了来自 188 例 UM 患者(170 例无转移患者;18 例临床可检测转移患者)和 18 例健康对照个体的血清样本中的 GDF-15 浓度。分析了患者之间有无临床可检测 UM 转移的差异。进一步分析了 GDF-15 血清水平与组织学和多重连接依赖性探针扩增(MLPA)揭示的显著患者和肿瘤特征,以确定 3 号染色体拷贝数。通过免疫组织化学研究了 UM 中的 GDF-15 表达。
与无临床可检测 UM 转移的患者以及健康个体相比,具有临床可检测转移的患者的 GDF-15 血清水平明显更高(ANOVA;p < 0.001)。具有明显临床可检测转移的 UM 患者的 GDF-15 浓度明显高于处于缓解但无临床检测到 UM 转移的具有第二恶性肿瘤的 UM 患者(ANOVA;p < 0.001)。未观察到 GDF-15 血清浓度与临床、病理和遗传特征之间存在关联。在大多数肿瘤中,GDF-15 蛋白仅在少数 UM 细胞中表达。
我们的数据表明,GDF-15 可用作 UM 患者转移诊断的血清标志物。需要进一步收集和分析数据,以评估 GDF-15 在预测早期转移方面的可能预后作用。