首页> 美国卫生研究院文献>The Journal of Biological Chemistry >MicroRNA-372 Is Down-regulated and Targets Cyclin-dependent Kinase 2 (CDK2) and Cyclin A1 in Human Cervical Cancer Which May Contribute to Tumorigenesis
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MicroRNA-372 Is Down-regulated and Targets Cyclin-dependent Kinase 2 (CDK2) and Cyclin A1 in Human Cervical Cancer Which May Contribute to Tumorigenesis

机译:MicroRNA-372被下调并靶向人类宫颈癌中可能与肿瘤发生有关的细胞周期蛋白依赖性激酶2(CDK2)和细胞周期蛋白A1。

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摘要

MicroRNAs are a class of noncoding RNAs that are ∼22 nucleotides in length. MicroRNAs have been shown to play important roles in cell differentiation and in cancer. Recently, studies have shown that miR-372 is tumorigenic in human reproductive system cancers. However, we provide evidence that miR-372 acts as a tumor suppressor gene in cervical carcinoma. miR-372 was found down-regulated in cervical carcinoma tissues as compared with adjacent normal cervical tissues. Growth curve and FACS assays indicated that ectopic expression of miR-372 suppressed cell growth and induced arrest in the S/G2 phases of cell cycle in HeLa cells. We used bioinformatic predictions to determine that CDK2 and cyclin A1 were possible targets of miR-372 and confirmed this prediction using a fluorescent reporter assay. Taken together, these findings indicate that an anti-oncogenic role of miR-372 may be through control of cell growth and cell cycle progression by down-regulating the cell cycle genes CDK2 and cyclin A1.
机译:MicroRNA是一类非编码RNA,长度约为22个核苷酸。 MicroRNA已显示在细胞分化和癌症中起重要作用。最近,研究表明miR-372在人类生殖系统癌症中具有致瘤性。但是,我们提供的证据表明miR-372在宫颈癌中起着抑癌基因的作用。与邻近的正常宫颈组织相比,在宫颈癌组织中发现miR-372下调。生长曲线和FACS分析表明,miR-372的异位表达抑制了HeLa细胞的细胞生长并诱导了S / G2期细胞周期的阻滞。我们使用生物信息学预测来确定CDK2和细胞周期蛋白A1是miR-372的可能靶标,并使用荧光报告基因分析法证实了这一预测。综上所述,这些发现表明,miR-372的抗癌作用可能是通过下调细胞周期基因CDK2和细胞周期蛋白A1来控制细胞生长和细胞周期进程。

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