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The Differential Expression of miRNAs and a Preliminary Study on the Mechanism of miR-194-3p in Keloids

机译:miRNAs在瘢痕loid中的差异表达及miR-194-3p作用机理的初步研究

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摘要

The aim of this study was to detect abnormally expressed microRNA (miRNA) in keloids and to study their functions. The differential expression of miRNAs in keloids and normal tissue was detected by gene microarray. MiRNA expression was verified by real-time PCR. A luciferase reporter gene assay, western blot, and real-time PCR were used to detect the effect of miR-194-3p on RUNX2. An MTT assay and a transwell assay were used to detect the effect of miR-194-3p in both primary cultured fibroblasts and HKF cells. Related proteins were analysed by western blot and real-time PCR. The expression of miR-194-3p was lower in keloids, and MiR-194-3p was shown to target RUNX2 directly. MiR-194-3p inhibited the proliferation and migration of fibroblasts through the inhibition of CDK4 and MMP2. MiR-194-3p and RUNX2 may become new targets for the prevention and treatment of keloids.
机译:这项研究的目的是检测瘢痕loid中异常表达的微小RNA(miRNA)并研究其功能。通过基因芯片检测miRNA在瘢痕loid和正常组织中的差异表达。通过实时PCR验证了miRNA的表达。荧光素酶报告基因测定,免疫印迹和实时PCR用于检测miR-194-3p对RUNX2的作用。使用MTT测定法和transwell测定法检测miR-194-3p在原代培养的成纤维细胞和HKF细胞中的作用。通过蛋白质印迹和实时PCR分析相关蛋白。瘢痕loid中miR-194-3p的表达较低,而MiR-194-3p则直接靶向RUNX2。 MiR-194-3p通过抑制CDK4和MMP2抑制成纤维细胞的增殖和迁移。 MiR-194-3p和RUNX2可能成为预防和治疗瘢痕loid的新靶标。

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