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RWR-algorithm-based dissection of microRNA-506-3p and microRNA-140-5p as radiosensitive biomarkers in colorectal cancer

机译:基于RWR-Algorithm的MicroRNA-506-3P和MicroRNA-140-5P的溶解作为结肠直肠癌中的辐射敏感生物标志物

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摘要

Radiotherapy resistance is one of the main causes for treatment failure in colorectal cancer (CRC), and it is associated with the deregulation of certain microRNAs. In this study, we constructed the microRNA-mRNA network consisting of 2275 microRNAs and 7045 target genes, collected the known microRNAs related to CRC-radiosensitivity (CRCR) (n=18) as the seed nodes, and applied the algorithm of random walk with restart (RWR) to the network to identify novel CRCR-related microRNAs (n=263). In functional analysis, 263 novel microRNAs shared a high proportion of the same biological processes and pathways with the known microRNAs. In topological analysis of the sub-network of the 263 microRNAs and their targets, hsa-mir-506-3p and hsa-mir-140-5p were identified as network hub nodes. In plasma, radiosensitive patients had a higher expression level of hsa-mir-506-3p and hsa-mir-140-5p than radioresistant patients. In experimental validation, both hsa-mir-506-3p and hsa-mir-140-5p over-expression could obviously decrease the cell proliferation, survival rate and colonality in CRC cells after radiation. In conclusion, this study combined the novel network-based method with experimental validation, and identified two novel radiosensitive biomarkers of hsa-mir-506-3p and hsa-mir-140-5p in CRC.
机译:放射疗法抗性是结直肠癌(CRC)治疗失败的主要原因之一,它与某些微小RNA的放松管制有关。在这项研究中,我们构建了由2275 microRNA和7045个靶基因组成的MicroRNA-mRNA网络,收集了与CRC-放射敏感性(CRCR)(n = 18)相关的已知的微小RNA,作为种子节点,并用随机行走算法重新启动(RWR)到网络以识别新的CRCR相关的MicroRNA(n = 263)。在功能性分析中,263个新的MicroRNA分享了相同的相同生物过程和具有已知微小RNA的途径的高比例。在263 microRNA的子网及其目标的拓扑分析中,将HSA-MIR-506-3P和HSA-MIR-140-5P识别为网络集线器节点。在血浆中,放射敏感性患者的表达水平较高,HSA-miR-506-3p和HSA-miR-140-5p的表达水平比放射患者患者。在实验验证中,HSA-MIR-506-3P和HSA-MIR-140-5P过度表达可明显降低CRC细胞中CRC细胞中的细胞增殖,存活率和结核性。总之,本研究结合了实验验证的新型网络的方法,并鉴定了CRC中HSA-miR-506-3P和HSA-MIR-140-5P的两种新型辐射敏感生物标志物。

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