Liu Jin, Wang Chuifang, Liu Xiangyan, Wang Yu, Liu Haibo, Ren Guohua, Zhu Liangming, Sun Zhigang, Chen Zhitao
Department of Gastroenterology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong 250021, P.R. China.
Department of Thoracic Surgery, Liaocheng Tumor Hospital, Liaocheng, Shandong 252000, P.R. China.
Oncol Lett. 2017 Jun;13(6):4469-4474. doi: 10.3892/ol.2017.5957. Epub 2017 Mar 30.
Recent studies have demonstrated that deregulated microRNA (miRNA/miR) expression has a profound impact on biological and pathological processes; abnormal miR-1469 expression was detected in several human malignancies. In the present study, the clinicopathological and prognostic significance of miR-1469 was assessed in 129 patients with esophageal squamous cell cancer (ESCC) who successfully underwent esophagectomy and esophagogastrostomy. Low miR-1469 expression was identified to be significantly associated with tumor invasion depth (P=0.026), lymph node metastasis status (P<0.001) and pathological tumor stage (P<0.001). Survival analysis demonstrated that patients with low miR-1469 expression had significantly poorer disease-free survival (DFS) (18.2 vs. 43.2%; P=0.004) and overall survival (29.1 vs. 47.3%; P=0.029) 5 years following surgery compared with patients with high miR-1469 expression. Univariate survival analysis demonstrated that low miR-1469 expression significantly predicted unfavorable 5-year DFS among patients with N1-3 disease (7.1 vs. 31.8%; P=0.043). The results from the present study indicate that miR-1469 expression could be used in the clinic to predict ESCC progression and prognosis. This will aid in the identification of high-risk patients with ESCC that require more aggressive therapeutic interventions.
近期研究表明,微小RNA(miRNA/miR)表达失调对生物学和病理过程具有深远影响;在多种人类恶性肿瘤中均检测到miR-1469表达异常。在本研究中,对129例行食管切除术和食管胃吻合术成功的食管鳞状细胞癌(ESCC)患者评估了miR-1469的临床病理及预后意义。结果发现,miR-1469低表达与肿瘤浸润深度(P=0.026)、淋巴结转移状态(P<0.001)及病理肿瘤分期(P<0.001)显著相关。生存分析表明,与miR-1469高表达患者相比,miR-1469低表达患者术后5年无病生存率(DFS)(18.2%对43.2%;P=0.004)和总生存率(29.1%对47.3%;P=0.029)明显较差。单因素生存分析表明,miR-1469低表达显著预测N1-3期患者5年DFS不良(7.1%对31.8%;P=0.043)。本研究结果表明,miR-1469表达可用于临床预测ESCC进展及预后。这将有助于识别需要更积极治疗干预的ESCC高危患者。