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MIR-192 AND MIR-215 INHIBIT NUCLEOTIDE EXCISION REPAIR BY TARGETING ERCC3 IN A549 CELL LINE

机译:靶向ERCC3在A549细胞株中的MIR-192和MIR-215抑制核苷酸兴奋修复

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Ionizing radiation(IR) plays an important role in the comprehensive therapy of non-small cell lung cancer, it can interfere the homeostasis of intracellular environment by extremely complex mechanisms, one of the most important one is to change the level of gene expression. MicroRNAs, which act at the posttranscriptional level via an RNA interference mechanism, is involved in the process of radiationinduced damage and repair, but the definite regulatory mechanism of microRNAs is still not clear. In this study, we investigated the expression level of miR-192,miR-215 and the protein ERCC3 in human lung carcinoma cell line A549 after radiation with 20Gy and 40Gy. Data analysis revealed that miR-192, miR-215 and ERCC3 protein consistently responded to ionizing radiation(IR),miR-192 and miR-215 were upregulated, and ERCC3 protein was down-regulated. We concluded that radiation ray may down regulate the expression of ERCC3 through up regulate the expression of miR-192 and miR-215,and then regulate the process of DNA damage and repair.
机译:电离辐射(IR)在非小细胞肺癌的综合治疗中起着重要作用,它可以通过极其复杂的机制干扰细胞内环境的稳态,其中最重要的之一就是改变基因表达水平。通过RNA干扰机制在转录后水平起作用的MicroRNA参与了辐射诱导的损伤和修复过程,但对microRNA的确定调控机制仍不清楚。在这项研究中,我们研究了用20Gy和40Gy辐射后人肺癌细胞系A549中miR-192,miR-215和ERCC3蛋白的表达水平。数据分析表明,miR-192,miR-215和ERCC3蛋白始终对电离辐射反应,miR-192和miR-215被上调,而ERCC3蛋白被下调。结论:放射线可能通过上调miR-192和miR-215的表达来下调ERCC3的表达,进而调控DNA的损伤和修复过程。

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