首页|circ_0000515靶向miR-924调控卵巢癌SKOV3细胞增殖、迁移及侵袭的机制研究

circ_0000515靶向miR-924调控卵巢癌SKOV3细胞增殖、迁移及侵袭的机制研究

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目的 探讨circ_0000515调控卵巢癌SKOV3细胞增殖、迁移及侵袭的分子机制.方法 采用qRT-PCR法检测circ_0000515、miR-924的表达量;体外培养人卵巢癌细胞SKOV3,增殖、克隆形成、迁移及侵袭分别经CCK-8、平板克隆形成、划痕与Transwell实验分析;miR-924和circ_0000515的关系经双荧光素酶报告实验证实;Western blot检测蛋白表达量.结果 相对于癌旁组织,circ_0000515在卵巢癌组织中上调,而miR-924下调(P<0.05);与si-NC组比较,si-circ_0000515组细胞活力降低,细胞克隆形成数减少(P<0.05);与si-NC组比较,si-circ_0000515组的划痕愈合率、侵袭细胞数、N-cadherin蛋白水平均降低,E-cadherin蛋白水平升高,差异有统计学意义(P<0.05);与miR-NC组比较,miR-924 组的 WT-circ_0000515 降低(P<0.05);与 pcDNA 组比较,pcDNA-circ_0000515 组的 miR-924 升高,与si-NC组比较,si-circ_0000515组的miR-924升高,差异有统计学意义(P<0.05);与miR-NC组比较,miR-924组细胞活力、划痕愈合率和N-cadherin蛋白水平降低,细胞克隆形成数和侵袭细胞数减少,E-cadherin蛋白水平升高(P<0.05);与 si-circ_0000515+anti-miR-NC 组比较,si-circ_0000515+anti-miR-924 组细胞活力、划痕愈合率和 N-cadherin 蛋白水平中升高,细胞克隆形成数和侵袭细胞数增多,E-cadherin蛋白水平降低(P<0.05).结论 circ_0000515沉默通过靶标miR-924抑制卵巢癌细胞恶性行为.
Study on the mechanism of circ_0000515 regulating proliferation,migration and invasion of ovarian cancer SKOV3 cells by targeting miR-924
Objective To explore the molecular mechanism of circ_0000515 regulating the proliferation,migration and invasion of ovarian cancer SKOV3 cells.Methods qRT-PCR method was used to detect the expression levels of circ_0000515 and miR-924.Human ovarian cancer cell SKOV3 was cultured in vitro.CCK-8 method,plate clone formation test,scratch test and Transwell test were used to analyze the proliferation,clone formation,migration and invasion of the cell.The relationship between miR-924 and circ_0000515 was confirmed by dual luciferase reporter experiments.Western blot was used to detect protein expression levels.Results Compared to paracancerous tissue,circ_0000515 expression was upregulated in ovarian cancer tissue,while miR-924 expression was downregulated(P<0.05).Compared with the si-NC group,the cell viability and the number of cell clones in the si-circ 0000515 group were decreased(P<0.05).Compared with the si-NC group,in the si-circ_0000515 group,the scratch healing rate,number of invasive cells,and N-cadherin protein level decreased,while the E-cadherin protein level increased,and there was statistically significant difference(P<0.05).Compared with the miR-NC group,WT-circ 0000515 expression in the miR-924 group decreased(P<0.05).Compared with the pcDNA group,mir-924 expression in the pcDNA-circ 0000515 group was increased,while compared with the si-NC group,miR-924 expression in the si-circ 0000515 group was increased,and there was statistically significant difference(P<0.05).Compared with the miR-NC group,the cell viability,scratch healing rate,and N-cadherin protein level in the miR-924 group decreased,while the number of cell clones and invasive cells decreased,and the E-cadherin protein level increased(P<0.05).Compared with the si-circ 0000515+anti miR-NC group,the cell viability,scratch healing rate,and N-cadherin protein level were increased in the si-circ 0000515+anti miR-924 group;The number of cell clones and invasive cells increased,while the E-cadherin protein level decreased(P<0.05).Conclusion Circ_0000515 silence inhibits the malignant behavior of ovarian cancer cells by targeting miR-924.

ovarian cancercirc_0000515miR-924cell proliferationmigrationinvasion

张瑛琦

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佳木斯市妇幼保健院,黑龙江佳木斯 154003

卵巢癌 circ_0000515 miR-924 细胞增殖 迁移 侵袭

黑龙江省卫生健康委科研项目

2019-453

2024

长春中医药大学学报
长春中医药大学

长春中医药大学学报

CSTPCD
影响因子:0.916
ISSN:1007-4813
年,卷(期):2024.40(3)
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