Todorova Krassimira, Metodiev Metodi V, Metodieva Gergana, Mincheff Milcho, Fernández Nelson, Hayrabedyan Soren
Institute of Biology and Immunology of Reproduction "Acad. Kiril Bratanov", Laboratory of Reproductive OMICs Technologies, Bulgarian Academy of Sciences, 73 Tsarigradsko shosse blvd, 1113, Sofia, Bulgaria.
School of Biological Sciences, University of Essex, Colchester, UK.
Horm Cancer. 2017 Feb;8(1):28-48. doi: 10.1007/s12672-016-0279-9. Epub 2017 Jan 3.
Cancer progression is driven by genome instability incurred rearrangements such as transmembrane protease, serine 2 (TMPRSS2)/v-ets erythroblastosis virus E26 oncogene (ERG) that could possibly turn some of the tumor suppressor micro-RNAs into pro-oncogenic ones. Previously, we found dualistic miR-204 effects, acting either as a tumor suppressor or as an oncomiR in ERG fusion-dependent manner. Here, we provided further evidence for an important role of miR-204 for TMPRSS2/ERG and androgen receptor (AR) signaling modulation and fine tuning that prevents TMPRSS2/ERG overexpression in prostate cancer. Based on proximity-based ligation assay, we designed a novel method for detection of TMPRSS2/ERG protein products. We found that miR-204 is TMPRSS2/ERG oncofusion negative regulator, and this was mediated by DNA methylation of TMPRSS2 promoter. Transcriptional factors runt-related transcription factor 2 (RUNX2) and ETS proto-oncogene 1 (ETS1) were positive regulators of TMPRSS2/ERG expression and promoter hypo-methylation. Clustering of patients' sera for fusion protein, transcript expression, and wild-type ERG transcript isoforms, demonstrated not all patients harboring fusion transcripts had fusion protein products, and only few fusion positive ones exhibited increased wild-type ERG transcripts. miR-204 upregulated AR through direct promoter hypo-methylation, potentiated by the presence of ERG fusion and RUNX2 and ETS1. Proteomics studies provided evidence that miR-204 has dualistic role in AR cancer-related reprogramming, promoting prostate cancer-related androgen-responsive genes and AR target genes, as well as AR co-regulatory molecules. miR-204 methylation regulation was supported by changes in molecules responsible for chromatin remodeling, DNA methylation, and its regulation. In summary, miR-204 is a mild regulator of the AR function during the phase of preserved AR sensitivity as the latter one is required for ERG-fusion translocation.
癌症进展由基因组不稳定性引发的重排驱动,如跨膜蛋白酶丝氨酸2(TMPRSS2)/ v -ets成红细胞增多症病毒E26癌基因(ERG),这可能会使一些肿瘤抑制性微小RNA转变为促癌性微小RNA。此前,我们发现了miR - 204的二元效应,它在ERG融合依赖的方式中既作为肿瘤抑制因子,又作为癌基因微小RNA发挥作用。在此,我们进一步提供证据表明,miR - 204在TMPRSS2 / ERG和雄激素受体(AR)信号调节及微调中起重要作用,可防止前列腺癌中TMPRSS2 / ERG的过表达。基于邻近连接分析,我们设计了一种检测TMPRSS2 / ERG蛋白产物的新方法。我们发现miR - 204是TMPRSS2 / ERG癌融合负调节因子,这是由TMPRSS2启动子的DNA甲基化介导的。转录因子 runt相关转录因子2(RUNX2)和ETS原癌基因1(ETS1)是TMPRSS2 / ERG表达和启动子低甲基化的正调节因子。对患者血清中融合蛋白、转录本表达和野生型ERG转录本异构体进行聚类分析表明,并非所有携带融合转录本的患者都有融合蛋白产物,只有少数融合阳性患者表现出野生型ERG转录本增加。miR - 204通过直接启动子低甲基化上调AR,ERG融合以及RUNX2和ETS1的存在可增强这种作用。蛋白质组学研究提供证据表明,miR - 204在AR癌症相关重编程中具有二元作用,促进前列腺癌相关雄激素反应基因和AR靶基因以及AR共调节分子。负责染色质重塑、DNA甲基化及其调节的分子变化支持了miR - 204的甲基化调节。总之,在保留AR敏感性的阶段,miR - 204是AR功能的温和调节因子,因为后者是ERG融合易位所必需的。