Institut für Klinische Chemie und Laboratoriumsmedizin, Medizinische Fakultät "Carl Gustav Carus", Technische Universität Dresden, Fetscherstrasse 74, 01307, Dresden, Germany,
Pathol Oncol Res. 2013 Oct;19(4):839-46. doi: 10.1007/s12253-013-9652-y. Epub 2013 Jun 1.
It is well-known that the plasma level of group IIA phospholipase A2 (sPLA2-IIA) is increased in patients with malignant diseases, but whether the up-regulated enzyme expression is directly related to tumorigenesis or a consequence of tumor-associated inflammation remains unresolved. In this study we analyzed circulating levels of sPLA2-IIA, C-reactive protein (CRP), fibrinogen, factor VIII (FVIII), von Willebrand factor (vWF), and antithrombin as biomarkers of inflammation and coagulation in patients with various types of malignancies. Underlying tumor entities were lung, esophageal, gastric, pancreatic, colorectal, head and neck, and hepatocellular carcinomas as well as multiple myeloma and non-Hodgkin's lymphoma. Plasma levels of sPLA2-IIA are shown to be markedly increased in all types of analysed malignancies in comparison to the normal range (22.8 ± 4.5 μg/L versus <1.9 μg/L). Levels of sPLA2-IIA correlate positively with CRP (p < 0.001), fibrinogen (p < 0.01), FVIII (p < 0.05), and vWF (p < 0.05) and negatively with antithrombin levels (p < 0.05). Kaplan-Meier analyses revealed a statistically prolonged survival time of patients with lower sPLA2-IIA concentrations (<4 μg/L) in comparison to those with elevated concentrations (>4 μg/L) of this enzyme. In conclusion, the study shows that the measurement of plasma sPLA2-IIA levels has prognostic values in patients with different types of malignancies. The association of sPLA2-IIA levels with CRP, fibrinogen, FVIII, and vWF levels supports the importance of inflammatory processes for the up-regulation of sPLA2-IIA during cancer progression.
众所周知,IIA 组磷脂酶 A2(sPLA2-IIA)的血浆水平在恶性疾病患者中升高,但上调的酶表达是否与肿瘤发生直接相关或与肿瘤相关炎症的后果有关仍未解决。在这项研究中,我们分析了循环 sPLA2-IIA、C 反应蛋白(CRP)、纤维蛋白原、因子 VIII(FVIII)、血管性血友病因子(vWF)和抗凝血酶作为各种类型恶性肿瘤炎症和凝血的生物标志物的水平。潜在的肿瘤实体是肺癌、食管癌、胃癌、胰腺癌、结直肠癌、头颈部癌以及肝细胞癌和非霍奇金淋巴瘤。与正常范围(22.8 ± 4.5 μg/L 与 <1.9 μg/L)相比,所有分析的恶性肿瘤类型中的 sPLA2-IIA 血浆水平均显著升高。sPLA2-IIA 水平与 CRP(p < 0.001)、纤维蛋白原(p < 0.01)、FVIII(p < 0.05)和 vWF(p < 0.05)呈正相关,与抗凝血酶水平呈负相关(p < 0.05)。Kaplan-Meier 分析显示,与 sPLA2-IIA 浓度升高(>4 μg/L)的患者相比,浓度较低(<4 μg/L)的患者具有统计学上更长的生存时间。总之,该研究表明,测量血浆 sPLA2-IIA 水平在不同类型恶性肿瘤患者中具有预后价值。sPLA2-IIA 水平与 CRP、纤维蛋白原、FVIII 和 vWF 水平的关联支持炎症过程在癌症进展过程中上调 sPLA2-IIA 的重要性。