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首页> 外文期刊>Cancer Cell International >MicroRNA-222 influences migration and invasion through MIA3 in colorectal cancer
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MicroRNA-222 influences migration and invasion through MIA3 in colorectal cancer

机译:MicroRNA-222通过MIA3影响结直肠癌的迁移和侵袭

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Background miR-222 has been reported to be overexpressed in colorectal cancer and it influences cancer cell proliferation, drug resistance and metastasis. However, the underlying molecular mechanism of miR-222 in colorectal cancer cell invasion and migration has not been thoroughly elucidated to date. Methods The cell cycle distribution and apoptosis were assessed by flow cytometry. Cell migration and invasion were analyzed by Transwell assays. The possible target gene of miR-222 was searched and identified by bioinformatics, dual luciferase reporter assay and western blot analysis. The siRNA method was used to confirm the function of the target gene. Results Overexpression of miR-222 effectively promotes migration and invasion of colorectal cancer (CRC) cells in vitro. Bioinformatics and the dual luciferase reporter assay revealed that miR-222 specifically targeted the 3′-UTR of melanoma inhibitory activity member 3 (MIA3), down-regulating its expression at the protein level. Inhibition of MIA3 by siRNA enhanced the migration and invasion of CRC cell lines. Conclusions Our study showed that miR-222 enhances the migration and invasion in CRC cells, primarily by down-regulation of MIA3.
机译:已经报道了背景miR-222在结直肠癌中过表达,并且它影响癌细胞的增殖,耐药性和转移。然而,迄今为止,尚未充分阐明miR-222在大肠癌细胞侵袭和迁移中的潜在分子机制。方法采用流式细胞仪检测细胞周期分布和凋亡。通过Transwell测定法分析细胞迁移和侵袭。通过生物信息学,双重荧光素酶报告基因分析和蛋白质印迹分析,搜索和鉴定了miR-222的可能靶基因。 siRNA方法用于确认靶基因的功能。结果miR-222的过表达在体外有效促进结直肠癌(CRC)细胞的迁移和侵袭。生物信息学和双重荧光素酶报告基因检测结果表明,miR-222特异性靶向黑色素瘤抑制活性成员3(MIA3)的3'-UTR,在蛋白水平下调了其表达。 siRNA抑制MIA3增强了CRC细胞系的迁移和侵袭。结论我们的研究表明,miR-222主要通过下调MIA3来增强CRC细胞的迁移和侵袭。

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