Department of Gynaecology in Weifang Yidu Central Hospital, Wei Fang, ShanDong, China.
Eur Rev Med Pharmacol Sci. 2018 Jun;22(12):3713-3718. doi: 10.26355/eurrev_201806_15250.
CircRNAs have been recently identified as important regulators in tumors biological functions. However, the clinical significance of circHIPK3 in epithelial ovarian cancer (EOC) remains unknown.
The expression of circHIPK3 in EOC tumor tissues and adjacent noncancerous tissues was analyzed by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR). The association between circHIPK3 expression and clinicopathological factors was analyzed by using Chi-square test. Kaplan-Meier method and log-rank test were used to analyze the association of circHIPK3 expression with disease-free survival (DFS) and overall survival (OS) time of EOC patients. Univariate and multivariate Cox analysis was also performed.
We found that circHIPK3 was higher expressed in EOC tissues and cells compared to adjacent normal tissue and ovarian epithelium cell line, respectively. Higher circHIPK3 expression associated with lymph node invasion, FIGO stage, and worse DFS and OS of patients. Moreover, multivariate Cox analysis showed that higher circHIPK3 was an independent predictor of DFS and OS in EOC patients.
Thus, circHIPK3 may be a novel biomarker for predicting EOC prognosis.
CircRNAs 最近被鉴定为肿瘤生物学功能的重要调节因子。然而,circHIPK3 在卵巢上皮性癌(EOC)中的临床意义尚不清楚。
采用实时定量聚合酶链反应(qRT-PCR)分析 EOC 肿瘤组织和相邻非癌组织中 circHIPK3 的表达。采用卡方检验分析 circHIPK3 表达与临床病理因素的关系。Kaplan-Meier 法和对数秩检验分析 circHIPK3 表达与 EOC 患者无病生存(DFS)和总生存(OS)时间的关系。同时进行单因素和多因素 Cox 分析。
我们发现,与相邻正常组织和卵巢上皮细胞系相比,circHIPK3 在 EOC 组织和细胞中的表达水平更高。circHIPK3 高表达与淋巴结侵犯、FIGO 分期以及患者较差的 DFS 和 OS 相关。此外,多因素 Cox 分析表明,circHIPK3 高表达是 EOC 患者 DFS 和 OS 的独立预测因子。
因此,circHIPK3 可能是预测 EOC 预后的一种新型生物标志物。