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血清 miR-296-5p 和 miR-28-3p 对人类胃癌的诊断和预后价值。

Diagnostic and Prognostic Value of Serum miR-296-5p and miR-28-3p in Human Gastric Cancer.

机构信息

Department of Gastrointestinal Surgery, First Hospital of ShanXi Medical University, Taiyuan City, China.

出版信息

Cancer Biother Radiopharm. 2023 Mar;38(2):95-101. doi: 10.1089/cbr.2020.4144. Epub 2020 Sep 7.

Abstract

Previous studies reported the use of microRNAs (miRNAs) as diagnostic and/or prognostic biomarkers for various cancers, including gastric cancer (GC). This study evaluated the diagnostic and prognostic significance of serum miR-296-5p and miR-28-3p in GC. Serum samples of 90 patients with GC and 90 healthy individuals, and 20 pairs of tissue specimens from patients with GC were collected. The expression of miR-296-5p and miR-28-3p in both the serum and tissue samples were detected using quantitative real-time polymerase chain reaction analysis. The diagnostic and prognostic values of miR-296-5p and miR-28-3p were evaluated by using receiver operating characteristic curve and Kaplan-Meier analyses, respectively. Compared with the healthy controls, the expression of miR-296-5p in the serum and tissues of patients with GC was significantly upregulated, whereas that of miR-28-3p was significantly downregulated. High miR-296-5p and low miR-28-3p levels in the serum significantly correlated with larger tumor size (>5 cm), lymph node metastasis, and TNM stage III+IV. The area under the curve values of miR-296-5p and miR-28-3p were 0.919 and 0.911, respectively, with high sensitivity and specificity. Kaplan-Meier survival curves showed that patients with GC with high level of miR-296-5p or low level of miR-1236-3p in the serum had the poorest overall survival. COX analysis showed that lymphatic metastasis, high miR-296-5p expression, and low miR-28-3p expression are independent parameters indicating poor prognosis in GC. Our findings indicate that serum miR-296-5p and miR-28-3p levels are potential biomarkers in the diagnosis and prognosis of GC.

摘要

先前的研究报告称,microRNAs(miRNAs)可作为各种癌症(包括胃癌[GC])的诊断和/或预后生物标志物。本研究评估了血清 miR-296-5p 和 miR-28-3p 在 GC 中的诊断和预后意义。收集了 90 例 GC 患者和 90 例健康个体的血清样本,以及 20 对来自 GC 患者的组织标本。使用定量实时聚合酶链反应分析检测血清和组织样本中 miR-296-5p 和 miR-28-3p 的表达。通过使用接收器操作特征曲线和 Kaplan-Meier 分析分别评估 miR-296-5p 和 miR-28-3p 的诊断和预后价值。与健康对照组相比,GC 患者血清和组织中 miR-296-5p 的表达明显上调,而 miR-28-3p 的表达明显下调。血清中高 miR-296-5p 和低 miR-28-3p 水平与较大的肿瘤大小(>5cm)、淋巴结转移和 TNM 分期 III+IV 显著相关。miR-296-5p 和 miR-28-3p 的曲线下面积值分别为 0.919 和 0.911,具有较高的灵敏度和特异性。Kaplan-Meier 生存曲线显示,血清中 miR-296-5p 水平高或 miR-1236-3p 水平低的 GC 患者总体生存最差。COX 分析表明,淋巴转移、高 miR-296-5p 表达和低 miR-28-3p 表达是 GC 预后不良的独立参数。我们的研究结果表明,血清 miR-296-5p 和 miR-28-3p 水平是 GC 诊断和预后的潜在生物标志物。

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