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首页> 外文期刊>Cancer letters >MicroRNA miR-302 inhibits the tumorigenicity of endometrial cancer cells by suppression of Cyclin D1 and CDK1
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MicroRNA miR-302 inhibits the tumorigenicity of endometrial cancer cells by suppression of Cyclin D1 and CDK1

机译:MicroRNA miR-302通过抑制Cyclin D1和CDK1抑制子宫内膜癌细胞的致瘤性

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摘要

MicroRNA miR-302 has been found to induce some tumor cell lines to "transdifferentiate" into miRNA-induced pluripotent stem cells (mirPS), thereby inhibiting tumor cell proliferation and reducing tumorigenicity. This study firstly found that miR-302 inhibited the proliferation and migration of endometrial cell line, Ishikawa and HEC-1-B, and arrested cell cycle at the G2/M phase. In addition, miR-302 inhibited tumorigenicity in immunodeficient mice transplanted with Ishikawa cells. Microarray and Western blotting results showed that miR-302 significantly inhibited CDK1 and Cyclin D1 gene expression in Ishikawa cells. MiR-302 directly targeted Cyclin D1, but indirectly regulated CDK1 gene expression.
机译:已发现MicroRNA miR-302诱导某些肿瘤细胞系“转分化”为miRNA诱导的多能干细胞(mirPS),从而抑制肿瘤细胞增殖并降低致瘤性。这项研究首先发现miR-302抑制子宫内膜细胞系Ishikawa和HEC-1-B的增殖和迁移,并使细胞周期停滞在G2 / M期。此外,miR-302抑制了移植了Ishikawa细胞的免疫缺陷小鼠的致瘤性。芯片和蛋白质印迹结果表明,miR-302显着抑制石川细胞中CDK1和Cyclin D1基因的表达。 MiR-302直接靶向细胞周期蛋白D1,但间接调控CDK1基因表达。

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