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The miRNA Pull Out Assay as a Method to Validate the miR-28-5p Targets Identified in Other Tumor Contexts in Prostate Cancer

机译:miRNA抽出法作为验证在前列腺癌其他肿瘤环境中鉴定的miR-28-5p目标的方法

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摘要

miR-28-5p is an intragenic miRNA which is underexpressed in several tumor types showing a tumor suppressor (TS) activity. Routinely, the known miR-28-5p targets are validated in specific tumor contexts but it is unclear whether these targets are also being regulated in other tumor types. To this end, we adopted the miRNA pull out assay to capture the miR-28-5p targets in DU-145 prostate cancer (PCa) cells. Firstly, we demonstrated that miR-28-5p acts as a TS-miRNA in PCa, affecting cell proliferation, survival, and apoptosis. Secondly, we evaluated the enrichment of the 10 validated miR-28-5p targets in the pull out sample. We showed that E2F6, TEX-261, MAPK1, MPL, N4BP1, and RAP1B but not BAG1, OTUB1, MAD2L1, and p21 were significantly enriched, suggesting that not all the miR-28-5p targets are regulated by this miRNA in PCa. We then verified whether the miR-28-5p-interacting targets were regulated by this miRNA. We selected E2F6, the most enriched target in the pull out sample, and demonstrated that miR-28-5p downregulated E2F6 at the protein level suggesting that our approach was effective. In general terms, these findings support the miRNA pull out assay as a useful method to identify context-specific miRNA targets.
机译:miR-28-5p是一种基因内miRNA,在几种肿瘤类型中表达不足,表现出肿瘤抑制(TS)活性。通常,已知的miR-28-5p靶标已在特定的肿瘤环境中得到验证,但尚不清楚这些靶标是否也在其他肿瘤类型中得到调节。为此,我们采用了miRNA提取试验来捕获DU-145前列腺癌(PCa)细胞中的miR-28-5p目标。首先,我们证明了miR-28-5p在PCa中起TS-miRNA的作用,影响细胞的增殖,存活和凋亡。其次,我们评估了提取样品中10个经过验证的miR-28-5p目标的富集。我们发现E2F6,TEX-261,MAPK1,MPL,N4BP1和RAP1B显着富集,但BAG1,OTUB1,MAD2L1和p21却没有显着富集,这表明在PCa中并非所有的miR-28-5p靶标都受该miRNA调控。然后,我们验证了与miR-28-5p相互作用的靶标是否受此miRNA调控。我们选择了E2F6(拉出样品中最富集的靶标),并证明miR-28-5p在蛋白质水平上下调了E2F6,这表明我们的方法有效。概括而言,这些发现支持miRNA抽出测定法作为鉴定背景特异性miRNA靶标的有用方法。

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