Sakata Jun, Kajiyama Hiroaki, Suzuki Shiro, Utsumi Fumi, Niimi Kaoru, Sekiya Ryuichiro, Shibata Kiyosumi, Senga Takeshi, Kikkawa Fumitaka
Department of Obstetrics and Gynecology, Graduate School of Medicine, Nagoya University, Nagoya 466-8550, Japan.
Division of Tumor Biology, Graduate School of Medicine, Nagoya University, Nagoya 466-8550, Japan.
Oncol Lett. 2017 Oct;14(4):4287-4293. doi: 10.3892/ol.2017.6658. Epub 2017 Jul 24.
Several previous studies have revealed that the expression of zinc finger E-box binding homeobox 1 (ZEB1) in solid malignancies has an important significance on the clinical outcome of patients. However, the association between ZEB1 expression and survival in patients with epithelial ovarian carcinoma (EOC) remains unclear. The objective of the present study was to examine the extent of ZEB1 expression in EOC using immunohistochemical staining and investigate its association with patient outcome. A total of 40 patients with EOC initially treated with cytoreductive surgery and systematic chemotherapy were enrolled. ZEB1 expression was immunohistochemically categorized as negative, weak, moderate and strong according to the size of the staining area, and intensity. Subsequently, the associations between ZEB1 expression and recurrence/progression-free survival (RFS) rate were examined. The median age of patients in the current study was 54 years old (range, 22-72 years old). Among these patients, 15 (37.5%) exhibited International Federation of Gynecology and Obstetrics stage I disease, and 10 (25.0%), 13 (32.5%), and 2 (5%) had stage II, III, and IV disease, respectively. No patients with negative expression of ZEB1 experienced recurrence. In addition, ZEB1 expression was identified to be a significant predictor of a poorer RFS rate compared with negative expression (negative vs. weak, moderate and strong, P=0.0126). Furthermore, multivariate analyses revealed that moderate and strong ZEB1 expression levels were significant prognostic indicators of a poorer RFS rate in patients with EOC (hazard ratio, 2.265; 95% confidence interval, 1.072-8.021; P=0.0349). Confining analysis to patients with the clear-cell/mucinous histological type, those with moderate/strong ZEB1 expression demonstrated a significantly poorer RFS rate (P=0.0025). Positive ZEB1 expression may be an indicator to predict unfavorable RFS in patients with EOC.
先前的多项研究表明,锌指E盒结合同源框蛋白1(ZEB1)在实体恶性肿瘤中的表达对患者的临床结局具有重要意义。然而,ZEB1表达与上皮性卵巢癌(EOC)患者生存率之间的关联仍不清楚。本研究的目的是通过免疫组织化学染色检测EOC中ZEB1的表达程度,并研究其与患者预后的关系。总共纳入了40例最初接受细胞减灭术和系统化疗的EOC患者。根据染色区域大小和强度,ZEB1表达通过免疫组织化学分为阴性、弱阳性、中度阳性和强阳性。随后,研究了ZEB1表达与复发/无进展生存期(RFS)率之间的关联。本研究中患者的中位年龄为54岁(范围为22 - 72岁)。在这些患者中,15例(37.5%)表现为国际妇产科联盟I期疾病,10例(25.0%)、13例(32.5%)和2例(5%)分别患有II期、III期和IV期疾病。ZEB1表达阴性者均未复发。此外,与阴性表达相比,ZEB1表达被确定为RFS率较差的显著预测指标(阴性与弱阳性、中度阳性和强阳性相比,P = 0.0126)。此外,多因素分析显示,ZEB1中度和强表达水平是EOC患者RFS率较差的显著预后指标(风险比,2.265;95%置信区间,1.072 - 8.021;P = 0.0349)。将分析局限于透明细胞/黏液性组织学类型的患者,ZEB1中度/强表达者的RFS率显著较差(P = 0.0025)。ZEB1阳性表达可能是预测EOC患者RFS不良的一个指标。