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外泌体包裹的miR-31、miR-192和miR-375可作为胃癌的临床生物标志物。

Exosome-Encapsulated miR-31, miR-192, and miR-375 Serve as Clinical Biomarkers of Gastric Cancer.

作者信息

He Jing, Wu Jing, Dong Shiyang, Xu Jing, Wang Jian, Zhou Xin, Rao Zhuqing, Gao Wen

机构信息

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.

出版信息

J Oncol. 2023 Feb 16;2023:7335456. doi: 10.1155/2023/7335456. eCollection 2023.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b61/9950326/e4bbdfa2edb2/JO2023-7335456.001.jpg

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