Hoshino Isamu, Ishige Fumitaka, Iwatate Yosuke, Gunji Hisashi, Shiratori Fumiaki, Kuwayama Naoki, Nabeya Yoshihiro, Takeshita Nobuyoshi, Matsubara Hisahiro
Division of Gastroenterological Surgery, Chiba Cancer Center, Chuo-ku, Chiba 260-8717, Japan.
Department of Hepatobiliary and Pancreatic Surgery, Chiba Cancer Center, Chuo-ku, Chiba 260-8717, Japan.
Oncol Lett. 2020 Dec;20(6):350. doi: 10.3892/ol.2020.12213. Epub 2020 Oct 10.
The function of microRNAs (miRs) is associated with the development and progression of various malignancies, with miRs presenting stably in the serum. The current study assessed the role of miR-1246 and miR-106b in the serum of patients with esophageal squamous cell carcinoma (ESCC). A comprehensive microarray analysis of miR expression was performed using the serum of patients with ESCC, which were subsequently validated via reverse transcription-quantitative PCR. A total of 55 test samples were obtained from Chiba University and 101 validation samples were gained from Chiba Cancer Center. The results revealed that miR-1246 expression significantly increased and miR-106b expression significantly decreased in each cohort. Receiver operating characteristic analysis revealed that the area under the curve (AUC) value of miR-1246 was 0.816 (sensitivity, 72.7%; specificity, 69.2%) and 0.779 (sensitivity, 71.3%; specificity, 70.6%) for the test and validation cohorts, respectively. The AUC of miR-106b was 0.716 (sensitivity, 65.5%; specificity, 61.6%) and 0.815 (sensitivity, 74.3%; specificity, 73.5%), respectively. In addition, the AUC of the miR-1246/miR-106b ratio was 0.901 (sensitivity, 80.0%; specificity, 80.0%) and 0.903 (sensitivity, 82.1%; specificity, 82.3%), respectively, which indicated a higher diagnostic ability compared with that of miR-1246 or miR-106b alone. The high miR-1246/miR-106b ratio group was associated with clinicopathological factors such as depth of invasion, progression, lymph node metastasis, and poor prognosis. Therefore, effective biomarkers may be generated by combining individual miRs obtained by comprehensive analysis of ESCC patient sera.
微小RNA(miR)的功能与多种恶性肿瘤的发生发展相关,且miR在血清中稳定存在。本研究评估了miR-1246和miR-106b在食管鳞状细胞癌(ESCC)患者血清中的作用。使用ESCC患者的血清进行了miR表达的全面微阵列分析,随后通过逆转录定量PCR进行验证。共从千叶大学获得55个测试样本,从千叶癌症中心获得101个验证样本。结果显示,在每个队列中,miR-1246表达显著增加,miR-106b表达显著降低。受试者工作特征分析显示,miR-1246在测试队列和验证队列中的曲线下面积(AUC)值分别为0.816(敏感性,72.7%;特异性,69.2%)和0.779(敏感性,71.3%;特异性,70.6%)。miR-106b的AUC分别为0.716(敏感性,65.5%;特异性,61.6%)和0.815(敏感性,74.3%;特异性,73.5%)。此外,miR-1246/miR-106b比值的AUC分别为0.901(敏感性,80.0%;特异性,80.0%)和0.903(敏感性,82.1%;特异性,82.3%),这表明与单独的miR-1246或miR-106b相比,其诊断能力更高。高miR-1246/miR-106b比值组与侵袭深度、进展、淋巴结转移和预后不良等临床病理因素相关。因此,通过综合分析ESCC患者血清获得的单个miR组合可能产生有效的生物标志物。