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Expression patterns of microRNA-329 and its clinical performance in diagnosis and prognosis of breast cancer

机译:microRNA-329的表达模式及其在乳腺癌诊断和预后中的临床意义

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摘要

This study was aimed to assess the expression and clinical performance of microRNA-329 (miR-329) in breast cancer. We recruited 134 breast cancer patients and 70 healthy volunteers for this study. MiR-329 expression was estimated by quantitative real-time polymerase chain reaction. A receiver operating characteristic assay was performed to evaluate the diagnostic value of serum miR-329. In addition, the prognostic significance of miR-329 was evaluated through Kaplan–Meier survival and Cox regression analyses. According to quantitative real-time polymerase chain reaction, miR-329 expression was downregulated in cancerous samples compared with healthy and normal controls (P<0.01), and its expression in serum specimens positively correlated with its expression in tissue samples (R=0.493, P<0.001). The decreased expression of miR-329 correlated with lymph node metastasis (P=0.015) and TNM stage (P=0.003). A receiver operating characteristic curve with an area under the curve of 0.932 was constructed, indicating the high diagnostic accuracy of miR-329. From the survival and multivariate Cox assays, we found that downregulated miR-329 expression was associated with poor overall survival (log-rank P<0.001) and served as an independent prognostic factor (hazard ratio =2.987, 95% CI =1.681–5.308, and P<0.001). In silico analysis using The Cancer Genome Atlas confirmed that miR-329 expression was lower in breast cancer cases compared with normal controls (P<0.001) and could be an efficient biomarker for cancer patients. Down-regulated miR-329 expression was an effective diagnostic and prognostic biomarker, which could be used for targeted therapy in patients with breast cancer.
机译:这项研究旨在评估microRNA-329(miR-329)在乳腺癌中的表达和临床表现。我们招募了134名乳腺癌患者和70名健康志愿者。通过定量实时聚合酶链反应评估MiR-329表达。进行受试者工作特征分析以评估血清miR-329的诊断价值。另外,通过Kaplan–Meier生存率和Cox回归分析评估了miR-329的预后意义。根据定量实时聚合酶链反应,与健康对照组和正常对照组相比,癌变样本中的miR-329表达下调(P <0.01),并且其在血清样本中的表达与组织样本中的表达呈正相关(R = 0.493, P <0.001)。 miR-329的表达降低与淋巴结转移(P = 0.015)和TNM分期(P = 0.003)相关。构建了一个接收器工作特性曲线,其曲线下面积为0.932,这表明miR-329的诊断准确性很高。从生存率和多变量Cox分析中,我们发现下调的miR-329表达与较差的总体生存率相关(log-rank P <0.001),并作为独立的预后因素(危险比= 2.987,95%CI = 1.681–5.308) ,且P <0.001)。使用The Cancer Genome Atlas进行的计算机分析证实,与正常对照组相比,乳腺癌病例中的miR-329表达较低(P <0.001),并且可能是癌症患者的有效生物标志物。下调的miR-329表达是一种有效的诊断和预后生物标志物,可用于乳腺癌患者的靶向治疗。

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