Zhang Li, Xiang Ping, Han Xuan, Wu Liyong, Li Xuwen, Xiong Zhuyou
Department of Plastic and Reconstructive Surgery, First Affiliated Hospital of Bengbu Medical College Anhui, China.
Center for Laboratory Research, First Affiliated Hospital of Bengbu Medical College Anhui, China.
Int J Clin Exp Pathol. 2015 Sep 1;8(9):11446-51. eCollection 2015.
MicroRNA-20a (miRNA-20a or miR-20a) plays a key role in tumorigenesis and progression. But the prognostic value of miR-20a in cutaneous squamous cell carcinoma (CSCC) remains unclear. The aim of this study was to identify the association of miR-20a and the prognosis of CSCC patients.
The miR-20a expression was detected using quantitative real-time polymerase chain reaction (qRT-PCR) in 152 CSCC tissues and matched adjacent normal tissues. Kaplan-Meier and Cox regression analysis were utilized to determine the association of miR-20a with overall survival as well as the prognosis of CSCC patients.
The expression of miR-20a was lower in CSCC tissues compared with adjacent normal tissues (P=0.000). Moreover, the expression of miR-20a was closely correlated with TNM stage (P=0.013). Kaplan-Meier analysis showed that patients with low miR-20a expression had significantly poorer overall survival than those with high miR-20a expression (P<0.05). Multivariate analysis revealed that miR-20a expression (P=0.001, HR=3.262, 95% CI: 1.635-6.520) could influence the prognosis and might be an independent prognostic predictor in CSCC.
Our results indicated that low miR-20a expression was associated with tumor stage of CSCC and suggested that miR-20a expression would be a novel biomarker for predicting clinical outcomes in CSCC patients. The inhibition of miR-20a might even become a new therapeutic method for the treatment of CSCC.
微小RNA-20a(miRNA-20a或miR-20a)在肿瘤发生和发展中起关键作用。但miR-20a在皮肤鳞状细胞癌(CSCC)中的预后价值仍不清楚。本研究的目的是确定miR-20a与CSCC患者预后的关系。
采用定量实时聚合酶链反应(qRT-PCR)检测152例CSCC组织及配对的癌旁正常组织中miR-20a的表达。利用Kaplan-Meier和Cox回归分析确定miR-20a与总生存期以及CSCC患者预后的关系。
与癌旁正常组织相比,CSCC组织中miR-20a的表达较低(P = 0.000)。此外,miR-20a的表达与TNM分期密切相关(P = 0.013)。Kaplan-Meier分析显示,miR-20a低表达患者的总生存期明显低于miR-20a高表达患者(P < 0.05)。多因素分析显示,miR-20a表达(P = 0.001,HR = 3.262,95%CI:1.635 - 6.520)可影响预后,可能是CSCC的独立预后预测指标。
我们的结果表明,miR-20a低表达与CSCC的肿瘤分期相关,提示miR-20a表达可能是预测CSCC患者临床结局的新型生物标志物。抑制miR-20a甚至可能成为治疗CSCC的新方法。