Ren Xiaojuan, Zhang Hui, Cong Hui, Wang Xudong, Ni Hongbing, Shen Xianjuan, Ju Shaoqing
Department of Laboratory Medicine, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Laboratory Medicine Center, Nantong Tumor Hospital, #48 Qingnian Road, Nantong, 226001, JS, People's Republic of China.
Pathol Oncol Res. 2018 Oct;24(4):739-744. doi: 10.1007/s12253-018-0392-x. Epub 2018 Mar 8.
Epithelium ovarian cancer (EOC) is currently the prevalent malignant cancer worldwide. However, there is a lack of efficient biomarkers for EOC screening. Accumulating evidence reveals that serum miRNA detectable in various types of cancer. Therefore, we explore the diagnostic value of combined detection of plasma miR-193a-5p, HE4 and CA125 for EOC. Serum samples were collected from 45 patients with primary EOC, 30 patients with benign ovarian tumor patients and 40 healthy controls. The expression of serum miR-193a-5p was detected by real-time quantitative PCR, and serum HE4 and CA125 were detected by chemiluminescent immunoassay. Moreover, a diagnostic model combining miR-193a-5p, HE4 and CA125 or alone in EOC patients was evaluated by ROC curve analysis. The relative expression quantity (RQ) of serum miR-193a-5p in EOC patients, benign ovarian tumor patients and healthy control groups were 0.419 (0.093, 2.215), 3.667 (1.633, 6.691) and 1.130 (1.000, 7.087), respectively. The RQ of serum miR-193a-5p in EOC patients was significantly lower than that in benign ovarian tumor patients and healthy controls (both P < 0.001), and there was no significant difference between benign ovarian tumor patients and healthy controls (both P > 0.05). There was no significant correlation between serum miR-193-5p, HE4 and CA125 levels (both P > 0.05). Additionally a risk model for miR-193a-5p, HE4 and CA125 was correlated with Grading and Lymph node metastasis (P = 0.016, P = 0.029). The area under the receiver operating characteristic curve of a risk model for distinguishing EOC patients from healthy individuals was 0.996, which higher than any single biomarker. Combined detection of miR-193-5p, HE4 and CA125 by logistic regression analysis could greatly improved the diagnostic ability of EOC and may prove to be a candidate biomarker, providing new directions for further investigation.
上皮性卵巢癌(EOC)是目前全球流行的恶性肿瘤。然而,缺乏用于EOC筛查的有效生物标志物。越来越多的证据表明,血清miRNA可在各种类型的癌症中检测到。因此,我们探讨血浆miR-193a-5p、HE4和CA125联合检测对EOC的诊断价值。收集45例原发性EOC患者、30例卵巢良性肿瘤患者和40例健康对照者的血清样本。采用实时定量PCR检测血清miR-193a-5p的表达,采用化学发光免疫分析法检测血清HE4和CA125。此外,通过ROC曲线分析评估miR-193a-5p、HE4和CA125联合或单独在EOC患者中的诊断模型。EOC患者、卵巢良性肿瘤患者和健康对照组血清miR-193a-5p的相对表达量(RQ)分别为0.419(0.093,2.215)、3.667(1.633,6.691)和1.130(1.000,7.087)。EOC患者血清miR-193a-5p的RQ显著低于卵巢良性肿瘤患者和健康对照组(均P < 0.001),卵巢良性肿瘤患者和健康对照组之间无显著差异(均P > 0.05)。血清miR-193-5p、HE4和CA125水平之间无显著相关性(均P > 0.05)。此外,miR-193a-5p、HE4和CA125的风险模型与分级和淋巴结转移相关(P = 0.016,P = 0.029)。区分EOC患者与健康个体的风险模型的受试者操作特征曲线下面积为0.996,高于任何单一生物标志物。通过逻辑回归分析联合检测miR-193-5p、HE4和CA125可大大提高EOC的诊断能力,可能被证明是一种候选生物标志物,为进一步研究提供新方向。