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miR-584 Suppresses Invasion and Cell Migration of Thyroid Carcinoma by Regulating the Target Oncogene ROCK1

机译:miR-584通过调节靶癌基因ROCK1抑制甲状腺癌的侵袭和细胞迁移。

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Background: Uncovering the target gene of miR-584 to control thyroid carcinoma (TC) invasion and migration is of central importance in the diagnosis, treatment, and prognosis of TC. To validate whether miR-584 has a tumor-suppressive role in thyroid cancer cells by targeting ROCK1, a series of experiments were conducted to figure out the mechanism of action of miR-584. Material and Methods: Migration analyses and cell proliferation assays were performed using miR-584-transfected cells. The expression levels of miR-584 in TC were detected by using real-time polymerase chain reaction (PCR). Western blot analyses were conducted to find out the relationship between the tumor suppressor miR-584 and the target oncogene ROCK1 protein expression levels. Wound healing experiments were used to examine the relationships between miR-584 and the migration of thyroid cancer K1 cells and the effects of ROCK1 knockdown on K1 cell motility. Results: Our results demonstrate that altering the miR584 levels affects human thyroid cancer cell migration, but has no effect on cell proliferation. The relative ROCK-1 expression levels were 1 and 0.54 in the scrambled-sequence control group and the miR-584 group, respectively. K1 cells transfected with siRNA-ROCK-1 showed weaker cell migration than cells transfected with siRNA-NC (negative control); the cell motility ratios were 18% and 27%, respectively. Conclusion: These results indicate that miR-584 could inhibit the expression of ROCK1, and ROCK1 knockdown would further affect the migration ability of K1 cells. (C) 2015 S. Karger GmbH, Freiburg
机译:背景:发现miR-584的靶基因以控制甲状腺癌(TC)的侵袭和迁移在TC的诊断,治疗和预后中至关重要。为了通过靶向ROCK1验证miR-584在甲状腺癌细胞中是否具有抑癌作用,进行了一系列实验以弄清miR-584的作用机理。材料和方法:使用miR-584转染的细胞进行迁移分析和细胞增殖测定。使用实时聚合酶链反应(PCR)检测miR-584在TC中的表达水平。进行了蛋白质印迹分析,以发现肿瘤抑制物miR-584与目标癌基因ROCK1蛋白表达水平之间的关系。伤口愈合实验用于检查miR-584与甲状腺癌K1细胞迁移之间的关系以及ROCK1敲低对K1细胞运动性的影响。结果:我们的结果表明,改变miR584水平会影响人类甲状腺癌细胞的迁移,但对细胞增殖没有影响。在顺序控制组和miR-584组中,ROCK-1的相对表达水平分别为1和0.54。转染siRNA-ROCK-1的K1细胞比转染siRNA-NC的细胞迁移更弱(阴性对照)。细胞运动率分别为18%和27%。结论:这些结果表明miR-584可以抑制ROCK1的表达,而ROCK1的敲低将进一步影响K1细胞的迁移能力。 (C)2015 S.Karger GmbH,弗赖堡

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