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miR-1236-3p suppresses the migration and invasion by targeting KLF8 in lung adenocarcinoma A549?cells

机译:miR-1236-3p通过靶向KLF8在肺腺癌A549?细胞中抑制迁移和侵袭

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Abstract MicroRNAs (miRNAs) have a great effect on regulating tumor cell migration, invasion, proliferation and prognosis. However, the mechanism of miR-1236-3p on regulating carcinogenesis is still unknown. In this study, the expression of miR-1236-3p was lower in lung adenocarcinoma tissues than that in adjacent normal tissue. In lung adenocarcinoma A549?cell line, miR-1236-3p decreased ability of cell invasion and migration, furthermore, we show that KLF8 is targeted by miR-1236-3p, and expression of miR-1236-3p is negatively correlated with KLF8. Additionally, miR-1236-3p suppressed the expression of KLF8 and EMT (epithelial mesenchymal transition)-related genes. Overexpression of KLF8 can promote EMT-related genes at protein level. In conclusion, our results support the fact that miR-1236-3p acts as a tumor inhibitor in lung adenocarcinoma by suppressing the activity of KLF8, and it may play a critical role in the diagnosis and treatment of lung cancer. ]]>
机译:摘要MicroRNA(miRNA)对调节肿瘤细胞迁移,侵袭,增殖和预后具有很大的效果。 然而,miR-1236-3p对调节致癌作用的机制仍然未知。 在该研究中,miR-1236-3p的表达在肺腺癌组织中低于相邻的正常组织中的表达。 在肺腺癌A549?细胞系中,miR-1236-3p细胞侵袭和迁移能力降低,此外,我们表明KLF8由miR-1236-3p靶向,MiR-1236-3p的表达与KLF8负相关。 另外,MiR-1236-3P抑制了KLF8和EMT(上皮间充质转变)的表达式的基因。 KLF8的过度表达可以在蛋白质水平促进与EMT相关基因。 总之,我们的研究结果支持MiR-1236-3P通过抑制KLF8的活性作为肺腺癌中的肿瘤抑制剂,并且可能在肺癌的诊断和治疗中发挥关键作用。 ]]>

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