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miRNA-22 suppresses colon cancer cell migration and invasion by inhibiting the expression of T-cell lymphoma invasion and metastasis 1 and matrix metalloproteinases 2 and 9

机译:miRNA-22通过抑制T细胞淋巴瘤侵袭和转移1和基质金属蛋白酶2和9的表达来抑制结肠癌细胞的迁移和侵袭

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Emerging evidence has demonstrated the altered expression of mRNAs in cancer development and progression. In this study, the precise role of miRNA-22 (miR-22) in colon cancer cells was investigated. Upon transfection with a miR-22 expression vector, the viability of HCT-116 human colon cancer cells was significantly reduced and tumor cell migration and invasion capacity were also suppressed. Computational in silico analysis predicted that T-cell lymphoma invasion and metastasis 1 (TIAM1) is a target gene of miR-22. This was confirmed by qRT-PCR and western blotting, which showed that miR-22 expression inhibited TIAM1 mRNA and protein expression, respectively. In addition, the expression of proinvasive gene matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9) and pro-angiogenic protein vascular endothelial growth factor (VEGF) were also reduced by miR-22 expression. Collectively, these data suggest that miR-22 may act as a tumor suppressor in colon cancer, most likely by targeting TIAM1 expression.
机译:越来越多的证据表明,mRNA的表达在癌症的发展和进程中发生了改变。在这项研究中,研究了miRNA-22(miR-22)在结肠癌细胞中的确切作用。用miR-22表达载体转染后,HCT-116人结肠癌细胞的活力显着降低,肿瘤细胞迁移和侵袭能力也受到抑制。计算机计算机分析预测,T细胞淋巴瘤的侵袭和转移1(TIAM1)是miR-22的目标基因。通过qRT-PCR和Western blotting证实了这一点,这表明miR-22表达分别抑制TIAM1 mRNA和蛋白表达。此外,miR-22的表达还降低了侵袭性基因基质金属蛋白酶2和9(MMP-2和MMP-9)和促血管生成蛋白的血管内皮生长因子(VEGF)的表达。总的来说,这些数据表明miR-22可能在结肠癌中起着抑癌作用,最有可能通过靶向TIAM1表达。

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