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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >miR-219a-5p represses migration and invasion of osteosarcoma cells via targeting EYA2
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miR-219a-5p represses migration and invasion of osteosarcoma cells via targeting EYA2

机译:miR-219a-5p通过靶向eya2压制迁移和侵袭骨肉瘤细胞的迁移和侵袭

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摘要

EYA2 is the developmental transcription factor and phosphatase, playing an important role in numerous species in regulating cell death and differentiation. Recent studies showed that EYA2 is dysregulated and involved in the progression of various cancers. However, the expression and role of EYA2 in osteosarcoma remains unclear. Here, we found that EYA2 expression was evidently upregulated osteosarcoma (OS) tissue and cell lines. Next, we predicted EYA2-targeting miRNAs, which was further evaluated using a dual luciferase reporter assay. We found that miR-219a-5p significantly repressed EYA2 expression via binding to the 3-UTR of EYA2. Furthermore, overexpressed miR-219a-5p significantly repressed OS cell invasion and migration, which was reversed by overexpressed EYA2. While silenced miR-219a-5p induced OS cell invasion and migration, which was reversed by silenced EYA2. In conclusion, our study revealed that miR-219a-5p function as tumour suppressor regulates OS cell invasiveness by repressing EYA2 expression.
机译:EyA2是发育转录因子和磷酸酶,在许多调节细胞死亡和分化中的许多物种中发挥着重要作用。最近的研究表明,EyA2具有吸诵并参与各种癌症的进展。然而,EyA2在骨肉瘤中的表达和作用仍然不清楚。在这里,我们发现EyA2表达明显上调了骨肉瘤(OS)组织和细胞系。接下来,我们预测eAA2靶向miRNA,其使用双荧光素酶报告分析进一步评估。我们发现MiR-219A-5P通过与EyA2的3-UTR结合而显着抑制EyA2表达。此外,过表达的miR-219a-5p显着压抑了OS细胞侵袭和迁移,其被过表达的眼镜逆转。虽然沉默的miR-219a-5p诱导的os细胞入侵和迁移,其被沉默的eaa2逆转。总之,我们的研究表明,通过抑制EyA2表达来调节肿瘤抑制剂的MIR-219A-5P功能。

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