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Screening and functional analysis of micro-RNAs that regulate the expression of the tumor suppression TP53 gene

机译:调控抑癌TP53基因表达的微小RNA的筛选与功能分析

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OBJECTIVE: With gradual increase of cancer incidence and mortality rates, the regulatory mechanism of cancer has become a hotspot. It has been known that the expression of TP53 is closely associated with the occurrence of cancer. The microRNA (miRNA)-mediated regulation of the expression of numerous proto-oncogenes has been reported. This study aimed to identify miRNAs that regulate the expression of TP53 gene. MATERIALS AND METHODS: The sequence of TP53 gene was downloaded from NCBI and analyzed with TargetScan software to predict potential miRNAs that regulate TP53 expression. miR-122 was selected as the most potential miRNA for regulating TP53. miR-122 mimics and inhibitor were synthesized and transfected into Hela cells. The expression of TP53 mRNA was measured by qRT-PCR. The cell proliferation, migration, and invasion ability were assessed by CCK-8, scratch wounding, and transwell invasion assay, respectively. RESULTS: Cells transfected with miR-122 mimics exhibited significantly lower TP53 expression (p 0.05). However, cells in miR-122 inhibitor group exhibited significantly higher TP53 expression (p 0.05). CONCLUSIONS: The selected miR-122 effectively inhibited the expression of TP53 gene in Hela cells, and enhanced their proliferation, migration, and invasion.
机译:目的:随着癌症发病率和死亡率的逐步提高,癌症的调控机制已成为研究热点。已知TP53的表达与癌症的发生密切相关。已经报道了microRNA(miRNA)介导的许多原癌基因表达的调节。这项研究旨在鉴定调节TP53基因表达的miRNA。材料与方法:TP53基因的序列是从NCBI下载的,并用TargetScan软件进行分析以预测可能调节TP53表达的miRNA。选择miR-122作为调节TP53最具潜力的miRNA。合成了miR-122模拟物和抑制剂并将其转染到Hela细胞中。通过qRT-PCR测量TP53 mRNA的表达。细胞增殖,迁移和侵袭能力分别通过CCK-8,刮伤和transwell侵袭测定来评估。结果:用miR-122模拟物转染的细胞显示TP53表达明显降低(p 0.05)。但是,miR-122抑制剂组中的细胞表现出明显更高的TP53表达(p 0.05)。结论:选择的miR-122可有效抑制TP53基因在Hela细胞中的表达,并增强其增殖,迁移和侵袭能力。

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