He Jing, Wu Jing, Dong Shiyang, Xu Jing, Wang Jian, Zhou Xin, Rao Zhuqing, Gao Wen
Department of Oncology, The First Affiliated Hospital of Nanjing Medical University/Jiangsu Province Hospital, Nanjing, China.
Department of Anesthesiology, The First Affiliated Hospital of Nanjing Medical University/Jiangsu Province Hospital, Nanjing, China.
J Oncol. 2023 Feb 16;2023:7335456. doi: 10.1155/2023/7335456. eCollection 2023.
In recent years, microRNAs (miRNAs) derived from exosomes have been attracting attention as novel clinical biomarkers in a variety of cancers. In this study, plasma samples from 60 gastric cancer (GC) patients and 63 healthy individuals were collected, and the exosomal microRNAs (ex-miRNAs) were isolated. We determined the specific ex-miRNAs through miRNA microarray and a database of differentially expressed miRNAs called dbDEMC. Then, the expression levels of exosomal miR-31, miR-192, and miR-375 were analyzed by quantitative polymerase chain reaction (qRT-PCR). Compared to the matched controls, exosomal miR-31, miR-375, and miR-192 were significantly upregulated in GC patients. Also, they were found to be associated with gender, with miR-192 being significantly upregulated in male GC patients. Kaplan-Meier analysis indicated that high expressions of exosomal miR-31, miR-375, and miR-192 were positively correlated with poor clinical outcomes of GC patients. Cox univariate and multivariate analysis found that ex-miR-375 expression and TNM stage were independent prognostic factors of overall survival (OS). Our findings revealed that exosomal miR-31, miR-192, and miR-375 might serve as noninvasive, sensitive, and specific biomarkers for the diagnosis and prognosis of GC patients.
近年来,源自外泌体的微小RNA(miRNA)作为多种癌症中的新型临床生物标志物备受关注。在本研究中,收集了60例胃癌(GC)患者和63例健康个体的血浆样本,并分离出了外泌体微小RNA(ex-miRNA)。我们通过miRNA微阵列和一个名为dbDEMC的差异表达miRNA数据库确定了特定的ex-miRNA。然后,通过定量聚合酶链反应(qRT-PCR)分析了外泌体miR-31、miR-192和miR-375的表达水平。与匹配的对照组相比,GC患者中外泌体miR-31、miR-375和miR-192显著上调。此外,发现它们与性别有关,miR-192在男性GC患者中显著上调。Kaplan-Meier分析表明,外泌体miR-31、miR-375和miR-192的高表达与GC患者不良的临床结局呈正相关。Cox单因素和多因素分析发现,ex-miR-375表达和TNM分期是总生存期(OS)的独立预后因素。我们的研究结果表明,外泌体miR-31、miR-192和miR-375可能作为GC患者诊断和预后的非侵入性、敏感且特异的生物标志物。