Shi Zhenfeng, Kadeer Aihemaiti, Wang Mopei, Wen Bin, Li Min, Huang Jinxing, Gao Yang, Liu Enwei, Liu Donghong, Jia Deyong, Liang Chengyuan
Department of Urology, The People's Hospital of Xinjiang Uyghur Autonomous Region, Urumqi 830002, Xinjiang, PR China.
Department of Oncology, Peking University Third Hospital, 49 North Garden Rd., Haidian District, 100191, Beijing, PR China.
Pathol Res Pract. 2019 Feb;215(2):354-357. doi: 10.1016/j.prp.2018.11.018. Epub 2018 Nov 24.
MicroRNAs (miRNAs) are single-stranded, endogenous, non-coding RNAs that are increased or decreased in almost all cancer types, and they paly crucial roles in the tumorigenesis as well as development.
90 patients diagnosed with bladder cancer were enrolled in the present study. The bladder cancer tissues or adjacent normal tissues were obtained from the tumor area or adjacent normal zone. The expression level of miR-133b was examined by quantitative real-time polymerase chain reaction assay (qRT-PCR). Survival curves were displayed by the Kaplan-Meier method, and differences between two survival curves were calculated by the log-rank test.
The expression levels of miR-133b in bladder tissues were significantly decreased when compared with the matched adjacent normal bladder tissues (P < 0.05). Moreover, miR-133b expression levels are significantly associated with lymphatic invasion (P = 0.026), distant metastasis (P = 0.025), tumor grade (P = 0.038), as well as the muscle invasion status (P < 0.001). The log-rank test indicated that patients with decreased miR-133b expression underwent poorer overall survival (P = 0.007). Furthermore, multivariate Cox regression analysis showed that the expression level of miR-133b (P = 0.024) was an independent factor for predicting the overall survival in patients with bladder cancer.
The present study showed that miR-133b might be associated with bladder cancer progression, and its down-regulation might be a biomarker for poor prognosis of bladder cancer.
微小RNA(miRNA)是单链内源性非编码RNA,几乎在所有癌症类型中均有增减,在肿瘤发生和发展中起关键作用。
本研究纳入90例诊断为膀胱癌的患者。从肿瘤区域或相邻正常区域获取膀胱癌组织或相邻正常组织。通过定量实时聚合酶链反应分析(qRT-PCR)检测miR-133b的表达水平。采用Kaplan-Meier法绘制生存曲线,通过对数秩检验计算两条生存曲线之间的差异。
与配对的相邻正常膀胱组织相比,膀胱组织中miR-133b的表达水平显著降低(P < 0.05)。此外,miR-133b表达水平与淋巴浸润(P = 0.026)、远处转移(P = 0.025)、肿瘤分级(P = 0.038)以及肌肉浸润状态(P < 0.001)显著相关。对数秩检验表明,miR-133b表达降低的患者总生存期较差(P = 0.007)。此外,多因素Cox回归分析显示,miR-133b的表达水平(P = 0.024)是预测膀胱癌患者总生存期的独立因素。
本研究表明,miR-133b可能与膀胱癌进展相关,其下调可能是膀胱癌预后不良的生物标志物。