Tas Faruk, Karabulut Senem, Serilmez Murat, Ciftci Rumeysa, Duranyildiz Derya
Institute of Oncology, University of Istanbul, Capa, 34390, Istanbul, Turkey,
Tumour Biol. 2014 Apr;35(4):3327-31. doi: 10.1007/s13277-013-1438-z. Epub 2013 Nov 24.
Macrophage migration-inhibitory factor (MIF) plays an important role in the pathogenesis of multiple malignancies, and its expression strongly also affects outcomes of cancer patients. The objective of this study was to determine the clinical significance of serum levels of MIF in epithelial ovarian cancer (EOC) patients. A total of 50 patients with a pathologically confirmed diagnosis of EOC were enrolled into this study. Serum MIF concentrations were determined using the solid-phase sandwich ELISA method. Age- and sex-matched 30 healthy controls were included in the analysis. Median age of patients was 56.5 years old, range 22 to 83 years. Majority of the patients had an advanced disease (International Federation of Gynecologists and Obstetricians (FIGO) stages III and IV) (90%). Baseline serum MIF levels were significantly higher than those in the healthy control group (p = 0.005). No known clinical variables including histology, grade of histology, stage of disease, debulking surgery, and serum CA 125 levels were found to be correlated with serum MIF levels (p > 0.05). Only those chemotherapy-unresponsive patients had higher serum MIF levels compared with responsive ones (p = 0.02). Patients with elevated serum MIF concentrations had significantly unfavorable overall survival compared to those with lower levels (p = 0.01). However, a serum MIF level was found to play no prognostic role for progression-free survival (p = 0.09). In conclusion, serum levels of MIF have diagnostic, predictive, and prognostic roles in EOC patients.
巨噬细胞移动抑制因子(MIF)在多种恶性肿瘤的发病机制中起重要作用,其表达水平也强烈影响癌症患者的预后。本研究的目的是确定上皮性卵巢癌(EOC)患者血清中MIF水平的临床意义。本研究共纳入50例经病理确诊为EOC的患者。采用固相夹心酶联免疫吸附测定法测定血清MIF浓度。分析中纳入了30名年龄和性别匹配的健康对照者。患者的中位年龄为56.5岁,范围为22至83岁。大多数患者患有晚期疾病(国际妇产科联盟(FIGO)III期和IV期)(90%)。基线血清MIF水平显著高于健康对照组(p = 0.005)。未发现包括组织学、组织学分级、疾病分期、肿瘤细胞减灭术和血清CA 125水平在内的已知临床变量与血清MIF水平相关(p > 0.05)。只有那些化疗无反应的患者血清MIF水平高于有反应的患者(p = 0.02)。血清MIF浓度升高的患者与较低水平的患者相比,总生存期明显较差(p = 0.01)。然而,发现血清MIF水平对无进展生存期无预后作用(p = 0.09)。总之,血清MIF水平在EOC患者中具有诊断、预测和预后作用。