Pashaei Elnaz, Pashaei Elham, Ahmady Maryam, Ozen Mustafa, Aydin Nizamettin
Department of Computer Engineering, Yildiz Technical University, Istanbul, Turkey.
Department of Computer Engineering and IT, Payame Noor University, Tehran, Iran.
PLoS One. 2017 Jun 26;12(6):e0179543. doi: 10.1371/journal.pone.0179543. eCollection 2017.
Prostate cancer (PCa) is a leading reason of death in men and the most diagnosed malignancies in the western countries at the present time. After radical prostatectomy (RP), nearly 30% of men develop clinical recurrence with high serum prostate-specific antigen levels. An important challenge in PCa research is to identify effective predictors of tumor recurrence. The molecular alterations in microRNAs are associated with PCa initiation and progression. Several miRNA microarray studies have been conducted in recurrence PCa, but the results vary among different studies.
We conducted a meta-analysis of 6 available miRNA expression datasets to identify a panel of co-deregulated miRNA genes and overlapping biological processes. The meta-analysis was performed using the 'MetaDE' package, based on combined P-value approaches (adaptive weight and Fisher's methods), in R version 3.3.1.
Meta-analysis of six miRNA datasets revealed miR-125A, miR-199A-3P, miR-28-5P, miR-301B, miR-324-5P, miR-361-5P, miR-363*, miR-449A, miR-484, miR-498, miR-579, miR-637, miR-720, miR-874 and miR-98 are commonly upregulated miRNA genes, while miR-1, miR-133A, miR-133B, miR-137, miR-221, miR-340, miR-370, miR-449B, miR-489, miR-492, miR-496, miR-541, miR-572, miR-583, miR-606, miR-624, miR-636, miR-639, miR-661, miR-760, miR-890, and miR-939 are commonly downregulated miRNA genes in recurrent PCa samples in comparison to non-recurrent PCa samples. The network-based analysis showed that some of these miRNAs have an established prognostic significance in other cancers and can be actively involved in tumor growth. Gene ontology enrichment revealed many target genes of co-deregulated miRNAs are involved in "regulation of epithelial cell proliferation" and "tissue morphogenesis". Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis indicated that these miRNAs regulate cancer pathways. The PPI hub proteins analysis identified CTNNB1 as the most highly ranked hub protein. Besides, common pathway analysis showed that TCF3, MAX, MYC, CYP26A1, and SREBF1 significantly interact with those DE miRNA genes. The identified genes have been known as tumor suppressors and biomarkers which are closely related to several cancer types, such as colorectal cancer, breast cancer, PCa, gastric, and hepatocellular carcinomas. Additionally, it was shown that the combination of DE miRNAs can assist in the more specific detection of the PCa and prediction of biochemical recurrence (BCR).
We found that the identified miRNAs through meta-analysis are candidate predictive markers for recurrent PCa after radical prostatectomy.
前列腺癌(PCa)是男性死亡的主要原因,也是目前西方国家诊断最多的恶性肿瘤。根治性前列腺切除术(RP)后,近30%的男性会出现血清前列腺特异性抗原水平升高的临床复发。PCa研究中的一个重要挑战是确定肿瘤复发的有效预测指标。微小RNA(miRNA)的分子改变与PCa的发生和进展有关。已经对复发性PCa进行了几项miRNA微阵列研究,但不同研究的结果各不相同。
我们对6个可用的miRNA表达数据集进行了荟萃分析,以确定一组共同失调的miRNA基因和重叠的生物学过程。荟萃分析使用“MetaDE”软件包,基于组合P值方法(自适应权重和Fisher方法),在R 3.3.1版本中进行。
对六个miRNA数据集的荟萃分析显示,miR-125A、miR-199A-3P、miR-28-5P、miR-301B、miR-324-5P、miR-361-5P、miR-363*、miR-449A、miR-484、miR-498、miR-579、miR-637、miR-720、miR-874和miR-98是常见的上调miRNA基因,而与非复发性PCa样本相比,miR-1、miR-133A、miR-133B、miR-137、miR-221、miR-340、miR-370、miR-449B、miR-489、miR-492、miR-496、miR-541、miR-572、miR-583、miR-606、miR-624、miR-636、miR-639、miR-661、miR-760、miR-890和miR-939是复发性PCa样本中常见的下调miRNA基因。基于网络的分析表明,其中一些miRNA在其他癌症中具有既定的预后意义,并且可以积极参与肿瘤生长。基因本体富集显示,共同失调的miRNA的许多靶基因参与“上皮细胞增殖的调节”和“组织形态发生”。京都基因与基因组百科全书(KEGG)分析表明,这些miRNA调节癌症途径。蛋白质-蛋白质相互作用(PPI)枢纽蛋白分析确定β-连环蛋白(CTNNB1)为排名最高的枢纽蛋白。此外,共同途径分析表明,E2A蛋白(TCF3)、MAX、原癌基因(MYC)、细胞色素P450 26A1(CYP26A1)和固醇调节元件结合蛋白1(SREBF1)与那些差异表达(DE)miRNA基因显著相互作用。所鉴定的基因已被认为是与几种癌症类型密切相关的肿瘤抑制因子和生物标志物,如结直肠癌、乳腺癌、PCa、胃癌和肝细胞癌。此外,研究表明,DE miRNA的组合可以帮助更特异性地检测PCa和预测生化复发(BCR)。
我们发现,通过荟萃分析鉴定的miRNA是根治性前列腺切除术后复发性PCa的候选预测标志物。