Zhang Huihui, Qi Fan, Cao Youhan, Chen Minfeng, Zu Xiongbing
Department of Urology, The First Affiliated Hospital of University of South China, Hengyang, China (mainland).
Department of Urology, Xiangya Hospital, Central South University, Changsha, China (mainland).
Med Sci Monit. 2014 May 17;20:812-7. doi: 10.12659/MSM.890300.
Down-regulation of microRNA-101 (miR-101) expression has been linked to bladder transitional cell carcinoma (BTCC) development. However, the relationship between the expression of miR-101 in BTCC and a patient's prognosis has not yet been studied. Thus, we attempted to explore the correlation of miR-101 and clinicopathological factors of BTCC patients, and evaluate the impact of miR-101 on prognosis of BTCC.
In 88 samples of BTCC (n=72) and normal tissues (n=16), the expressions of miR-101 were detected by quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR). The relationship of miR-101 and clinicopathological factors in BTCC was analyzed statistically. Survival analysis was performed to assess the prognostic significance of miR-101.
Down-regulation of miR-101 was found in BTCC tissues, compared with normal tissues (P<0.05). MiR-101 expression was significantly associated with tumor diameter, tumor stage, tumor grade, lymph node involvement, and lymph node metastasis (all P<0.05). Low-level expression of miR-101 was significantly correlated with shortened survival time (P<0.01). Multivariate Cox regression analysis revealed this significant prognostic impact was independent of other clinicopathologic factors (P<0.01).
Our results suggest that the expression of miR-101 is down-regulated in BTCC, which consequently favored tumor progression. MiR-101 may play an important role as a diagnostic and prognostic marker in BTCC.
微小RNA - 101(miR - 101)表达下调与膀胱移行细胞癌(BTCC)的发生发展有关。然而,BTCC中miR - 101的表达与患者预后之间的关系尚未得到研究。因此,我们试图探讨miR - 101与BTCC患者临床病理因素的相关性,并评估miR - 101对BTCC预后的影响。
在88份BTCC样本(n = 72)和正常组织样本(n = 16)中,采用定量逆转录聚合酶链反应(qRT - PCR)检测miR - 101的表达。对BTCC中miR - 101与临床病理因素的关系进行统计学分析。进行生存分析以评估miR - 101的预后意义。
与正常组织相比,BTCC组织中miR - 101表达下调(P < 0.05)。miR - 101表达与肿瘤直径、肿瘤分期、肿瘤分级、淋巴结受累及淋巴结转移显著相关(均P < 0.05)。miR - 101低水平表达与生存时间缩短显著相关(P < 0.01)。多因素Cox回归分析显示,这种显著的预后影响独立于其他临床病理因素(P < 0.01)。
我们的结果表明,BTCC中miR - 101表达下调,这有利于肿瘤进展。miR - 101可能作为BTCC的诊断和预后标志物发挥重要作用。