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Up-regulation of microRNA-302a inhibited the proliferation and invasion of colorectal cancer cells by regulation of the MAPK and PI3K/Akt signaling pathways

机译:microRNA-302a的上调通过调节MAPK和PI3K / Akt信号通路抑制大肠癌细胞的增殖和侵袭

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摘要

Aberrant expression of microRNA-302a (miR-302a) has been frequently reported in some cancers excluding colorectal cancer (CRC). However, the role of miR-302a in CRC has not been reported. In this paper, we examined the effect of miR-302a overexpression on proliferation and invasion in CRC cells. The mRNA level of miR-302a in CRC cell lines was determined by real-time PCR. The miR-302a mimic was transiently transfected into CRC cells using Lipofectamine™ 2000 reagent. Subsequently, cell proliferation and invasion were assessed by MTT and Transwell assays. Western blot and ELISA assay were used to detect the expressions and secretions of matrix metalloproteinases (MMPs). Moreover, the expressions of epithelial marker, mesenchymal markers and transcription factors were also determined by Western blot. In addition, the effects of miR-302a overexpression on the MAPK and PI3K/Akt signaling pathways were investigated by Western blot. Our results showed that the mRNA level of miR-302a was remarkably decreased in CRC cell lines compared with normal colon epithelium cells. Up-regulation of miR-302a inhibited the proliferation and invasion of CRC cells. The expressions and secretions of MMP-9 and -2 were evidently reduced by increasing miR-302a. Besides, we found a decrease of β-catenin, fibronection, vimentin, Snail, Slug, ZEB1 and ZEB2 expressions and an increase of E-cadherin expression. We also found that miR-302a overexpression might decrease the phosphorylation of Erk1/2 and Akt. Altogether, our results indicated that miR-302a overexpression was shown to inhibit proliferation and invasion of CRC cells by reducing the expressions of related proteins through suppressing the MAPK and PI3K/Akt signaling pathways.
机译:MicroRNA-302a(miR-302a)的异常表达已在除结直肠癌(CRC)以外的某些癌症中频繁报道。但是,尚未报道miR-302a在CRC中的作用。在本文中,我们研究了miR-302a过表达对CRC细胞增殖和侵袭的影响。通过实时PCR确定CRC细胞系中miR-302a的mRNA水平。使用Lipofectamine™2000试剂将miR-302a模拟物瞬时转染到CRC细胞中。随后,通过MTT和Transwell测定评估细胞增殖和侵袭。 Western blot和ELISA法检测基质金属蛋白酶(MMPs)的表达和分泌。此外,还通过蛋白质印迹法测定上皮标志物,间充质标志物和转录因子的表达。另外,通过蛋白质印迹研究了miR-302a过表达对MAPK和PI3K / Akt信号通路的影响。我们的结果表明,与正常结肠上皮细胞相比,CRC细胞系中miR-302a的mRNA水平显着降低。 miR-302a的上调抑制了CRC细胞的增殖和侵袭。增加miR-302a可以明显降低MMP-9和-2的表达和分泌。此外,我们发现β-catenin,纤连蛋白,波形蛋白,Snail,Slug,ZEB1和ZEB2表达减少,而E-cadherin表达增加。我们还发现miR-302a过表达可能会降低Erk1 / 2和Akt的磷酸化。总之,我们的结果表明,miR-302a的过表达通过抑制MAPK和PI3K / Akt信号通路来减少相关蛋白的表达,从而抑制CRC细胞的增殖和侵袭。

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