Waseem Mohammad, Ahmad Mohammad Kaleem, Srivatava Vikas Kumar, Rastogi Namrata, Serajuddin Mohammad, Kumar Shashank, Mishra Durga Prasad, Sankhwar Satya Narain, Mahdi Abbas Ali
Molecular and Cell Biology, Department of Biochemistry, King George’s Medical University, Lucknow, U.P. India
Department of Urology, King George’s Medical University, Lucknow, U.P. India. Email:
Asian Pac J Cancer Prev. 2017 Aug 27;18(8):2185-2191. doi: 10.22034/APJCP.2017.18.8.2185.
Objective: MicroRNAs (miRs) are class of small non-coding regulatory RNA aberrantly expressed in various types of malignancies including prostate cancer and serves as potential targets to develop new diagnostic and therapeutic strategies. In this quiet we investigated miRNAs expression profile in benign prostatic hyperplasia (BPH) and prostate cancer (PCa) tissue samples and correlated their expression with clinicopathological parameters. Methodology: The miRNAs expression profile as well as their validation has been done by using Microarray and RT-PCR, respectively. Additionally, we also tried to speculate microRNA-mRNA regulatory module through computational target predictions by using Targetscan, Miranda and MirWalk and obtained results were analysed through DAVID software. Result: We observed that miR-711 is significantly deregulated in BPH and PCa, compared to controls. The lower expression of miR-711 was found to be significantly associated with high Gleason score and metastatic disease. Furthermore, the computational target prediction analysis explored miR-711 association to various cancer cells signalling cascade key molecules associated with cancer cell survival.Conclusion: From our observations we suggest that miR-711 may play a critical role in PCa progression, regulation of various cancer cell survival signalling cascades and that it may be a valuable biomarker for prediction of metastatic disease and poor prognosis in PCa.
微小RNA(miRs)是一类小的非编码调节性RNA,在包括前列腺癌在内的各种恶性肿瘤中异常表达,可作为开发新诊断和治疗策略的潜在靶点。在此研究中,我们调查了良性前列腺增生(BPH)和前列腺癌(PCa)组织样本中miRNAs的表达谱,并将它们的表达与临床病理参数相关联。方法:分别使用微阵列和逆转录-聚合酶链反应(RT-PCR)完成miRNAs表达谱及其验证。此外,我们还通过使用Targetscan、Miranda和MirWalk进行计算靶标预测来推测微小RNA-信使核糖核酸(miRNA-mRNA)调控模块,并通过DAVID软件分析获得的结果。结果:我们观察到,与对照组相比,miR-711在BPH和PCa中显著失调。发现miR-711的低表达与高Gleason评分和转移性疾病显著相关。此外,计算靶标预测分析探索了miR-711与各种癌细胞信号级联关键分子的关联,这些分子与癌细胞存活相关。结论:根据我们的观察,我们认为miR-711可能在PCa进展、各种癌细胞存活信号级联的调节中起关键作用,并且它可能是预测PCa转移性疾病和不良预后的有价值的生物标志物。