Dong Liang-Liang, Chen Li-Ming, Wang Wei-Min, Zhang Liang-Ming
Department of Medical Oncology, Yantai Yuhuangding Hospital, 20 Yuhuangding East Road, Yantai, Shandong, 264000, China.
Diagn Pathol. 2015 Apr 29;10:45. doi: 10.1186/s13000-015-0257-5.
MicroRNA-124 (miR-124) has been reported to be downregulated in breast cancer. However, its clinical significance and prognostic value in breast cancer have not been extensively studied.
The tissue expression levels of miR-124 were measured using quantitative real-time PCR in 133 breast cancer patients. The correlation between the miR-124 levels and the clinicopathological factors of the patients was also analyzed. Survival and Cox proportional-hazards regression analyses were performed to determine the correlation between miR-124 expression levels and prognosis in the patients.
Quantitative real-time PCR analysis showed that miR-124 had lower expression in breast cancer specimens than that in matched adjacent normal breast tissues (0.39 ± 0.16 vs. 1.00 ± 0.39; P < 0.05). Low miR-124 expression level was significantly associated with advanced TNM stage (P = 0.011), lymph node metastasis (P = 0.012), and poorer pathological differentiation (P = 0.023). A significant difference was found that breast cancer patients with low miR-124 expression level had distinctly shorter overall survival than patients with high miR-124 expression level (63.8% vs. 35.2%, P = 0.03). Furthermore, multivariate analysis of the prognosis factors with a Cox proportional hazards model confirmed that low miR-124 expression was a significant independent predictor of poor survival in breast cancer (HR = 3.16, 95% CI: 1.79-9.13, P = 0.017).
These findings proved that the decreased expression of miR-124 might be associated with tumor progression and poor prognosis in patients with breast cancer.
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据报道,微小RNA-124(miR-124)在乳腺癌中表达下调。然而,其在乳腺癌中的临床意义和预后价值尚未得到广泛研究。
采用定量实时PCR检测133例乳腺癌患者组织中miR-124的表达水平。分析miR-124水平与患者临床病理因素之间的相关性。进行生存分析和Cox比例风险回归分析,以确定miR-124表达水平与患者预后之间的相关性。
定量实时PCR分析显示,miR-124在乳腺癌标本中的表达低于配对的相邻正常乳腺组织(0.39±0.16 vs. 1.00±0.39;P<0.05)。miR-124低表达水平与晚期TNM分期(P=0.011)、淋巴结转移(P=0.012)及较差的病理分化(P=0.023)显著相关。发现miR-124低表达水平的乳腺癌患者总生存期明显短于miR-124高表达水平的患者(63.8% vs. 35.2%,P=0.03)。此外,用Cox比例风险模型对预后因素进行多因素分析证实,miR-124低表达是乳腺癌患者生存不良的重要独立预测因素(HR=3.16,95%CI:1.79-9.13,P=0.017)。
这些发现证明,miR-124表达降低可能与乳腺癌患者的肿瘤进展和不良预后有关。
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