Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, 466-8550, Japan.
Department of Surgery, Seoul National University College of Medicine, Seoul, Korea.
Gastric Cancer. 2020 Mar;23(2):203-211. doi: 10.1007/s10120-019-00995-z. Epub 2019 Aug 3.
Development of high-performance serum biomarkers will likely improve treatment outcomes of patients with gastric cancer (GC). We previously identified the candidate serum markers, anosmin 1 (ANOS1), dihydropyrimidinase-like 3 (DPYSL3), and melanoma-associated antigen D2 (MAGE-D2) and evaluated their clinical significance through a single-center retrospective analysis. Here we conducted a prospective multicenter observational study aimed at validating the diagnostic performance of these potential markers.
We analyzed serum levels before and after surgery of the three potential biomarkers in patients with GC and healthy volunteers. Quantification of serum and GC tissue levels was performed using an ELISA.
Area under the curve (AUC) values that discriminated patients with GC from healthy controls were - 0.7058, 0.6188, and 0.5031 for ANOS1, DPYSL3, and MAGED2, respectively. The sensitivity and specificity of the ANOS1 assay were 0.36 and 0.85, respectively. The AUC value of ANOS1 that discriminated patients with stage I GC from healthy controls was 0.7131. Serum ANOS1 levels were significantly elevated in patients with stage I GC compared with those of healthy controls (median 1179 ng/ml and 461 ng/ml, respectively, P < 0.0001) and decreased after resection of primary GC lesions (P < 0.0001). The combination of serum ANOS1 and DPYSL3 levels increased the AUC value that discriminated patients with GC from healthy controls. Serum levels of ANOS1 did not significantly correlate with those of carcinoembryonic antigen, carbohydrate antigen 19-9, or other markers of inflammation.
Serum levels of ANOS1 may serve as a useful diagnostic tool for managing GC.
开发高性能的血清生物标志物可能会改善胃癌(GC)患者的治疗效果。我们之前已经确定了候选血清标志物,anosmin 1(ANOS1)、二氢嘧啶酶样 3(DPYSL3)和黑色素瘤相关抗原 D2(MAGE-D2),并通过单中心回顾性分析评估了它们的临床意义。在这里,我们进行了一项前瞻性多中心观察性研究,旨在验证这些潜在标志物的诊断性能。
我们分析了 GC 患者和健康志愿者手术前后三种潜在生物标志物的血清水平。使用 ELISA 定量检测血清和 GC 组织水平。
区分 GC 患者和健康对照者的曲线下面积(AUC)值分别为 ANOS1、DPYSL3 和 MAGED2 的-0.7058、0.6188 和 0.5031。ANOS1 检测的灵敏度和特异性分别为 0.36 和 0.85。区分 I 期 GC 患者和健康对照者的 ANOS1 AUC 值为 0.7131。与健康对照组相比,I 期 GC 患者的血清 ANOS1 水平显著升高(中位数分别为 1179ng/ml 和 461ng/ml,P<0.0001),且原发性 GC 病变切除后降低(P<0.0001)。血清 ANOS1 和 DPYSL3 水平的联合检测增加了区分 GC 患者和健康对照者的 AUC 值。血清 ANOS1 水平与癌胚抗原、糖类抗原 19-9 或其他炎症标志物均无显著相关性。
血清 ANOS1 水平可能是 GC 管理的有用诊断工具。