Hospital of Clinical Medicine, Binzhou Medical University, Binzhou, Shandong, China.
Eur Rev Med Pharmacol Sci. 2018 Mar;22(6):1726-1730. doi: 10.26355/eurrev_201803_14587.
Previous study has reported that miR-330-3p was highly expressed in breast cancer (BC) patients. However, the effect of miR-330-3p in BC progression remains largely unclear. The purpose of this study was to investigate the clinical significance of miR-330-3p expression in BC.
The expression of miR-330-3p was detected by quantitative Real-time PCR in BC tissues and matched normal breast tissues. The association of miR-330-3p expression with clinicopathological factors of BC patients was also analyzed by x2-test. Prognosis value of patients with BC was assessed by Kaplan-Meier method and Cox proportional hazards model, respectively.
Quantitative real-time PCR analysis showed that the expression level of miR-330-3p was significantly higher in BC specimens than that in corresponding noncancerous tissues (p < 0.01). The levels of miR-330-3p were positively correlated with the status of TNM stage (p = 0.011) and lymph node metastasis (p = 0.006). Kaplan-Meier analysis revealed that 5-year overall survival of BC patients with high miR-330-3p expression was shorter compared to those patients with low miR-330-3p expression (p < 0.0001). Moreover, univariate and multivariate regression analysis demonstrated that miR-330-3p was an independent prognostic factor in BC.
Our data suggest that miR-330-3p upregulation maybe concurrently associated with prognosis in patients with BC, suggesting that miR-330-3p may be a potential prognostic biomarker and therapeutic target for patients with BC.
先前的研究报道 miR-330-3p 在乳腺癌(BC)患者中高表达。然而,miR-330-3p 在 BC 进展中的作用仍不清楚。本研究旨在探讨 miR-330-3p 表达在 BC 中的临床意义。
采用实时定量 PCR 检测 BC 组织和配对正常乳腺组织中 miR-330-3p 的表达。采用 x2 检验分析 miR-330-3p 表达与 BC 患者临床病理因素的关系。采用 Kaplan-Meier 法和 Cox 比例风险模型评估 BC 患者的预后价值。
实时定量 PCR 分析显示,BC 标本中 miR-330-3p 的表达水平明显高于相应的非癌组织(p<0.01)。miR-330-3p 的水平与 TNM 分期(p=0.011)和淋巴结转移(p=0.006)的状态呈正相关。Kaplan-Meier 分析显示,miR-330-3p 高表达的 BC 患者 5 年总生存率明显短于 miR-330-3p 低表达的患者(p<0.0001)。此外,单因素和多因素回归分析表明,miR-330-3p 是 BC 的独立预后因素。
我们的数据表明,miR-330-3p 的上调可能与 BC 患者的预后同时相关,表明 miR-330-3p 可能是 BC 患者潜在的预后生物标志物和治疗靶点。