miRNA-34a靶向Bcl-2对肝癌细胞HepG2的生长和迁移能力的影响
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黑龙江省卫生健康委科研课题(2019-299)


The effect of miRNA-34a targeting Bcl-2 on the growth and migration of hepatocarcinoma cell HepG2
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    摘要:

    通过过表达miRNA-34a检测Bcl-2的表达及对肝癌细胞的生长和迁移能力的影响,为肝癌的治疗提供新靶点。方法 通过生物信息学方法预测miRNA-34a的潜在作用靶点;采用双荧光素酶报告实验检测miRNA-34a与Bcl-2的靶向调控关系;体外培养肝癌细胞,将肝癌细胞分为对照组(转染miRNA-34a阴性对照物mimic NC)及miRNA-34a转染组(转染miRNA-34a模拟物)。分别转染miR-34a模拟物和阴性对照,转染36 h后,CCK8检测细胞增殖,Trans-well检测细胞迁移能力,q-PCR和Western blot方法检测miRNA-34a对肝癌细胞中Bcl-2表达量的影响。结果 miRNA-34a对肝癌HepG2细胞的活力和迁移能力具有抑制作用(P<0.01);miRNA-34a可以直接靶向下调Bcl-2(P<0.01)的表达。结论 miRNA-34a可靶向并负向调控Bcl-2,降低肝癌细胞HepG2的活力和迁移能力。

    Abstract:

    The overexpression of miRNA-34a was used to detect the expression of Bcl-2 and its effect on the growth and migration of liver cancer cells, and provided a new target for the treatment of liver cancer.Methods The potential targets of miRNA-34a were predicted by bioinformatics. The targeted regulation relationship between miRNA-34a and Bcl-2 was detected by double luciferase reporter experiment Hepatocellular carcinoma cells were cultured in vitro and transfected with miRNA-34a mimetic and negative control respectively. After 36 hours of transfection, CCK8 was used to detect cell proliferation, Trans well was used to detect cell migration ability, and q-PCR and Western blot were used to detect the effect of miRNA-34a on Bcl-2 expression in hepatocellular carcinoma cells. Results miRNA-34a could directly down regulate the expression of Bcl-2 (P<0.01). MiRNA-34a could inhibite the viability and migration of hepatocellular carcinoma HepG2 cells (P<0.01). Conclusion MiRNA-34a can target and negatively regulate Bcl-2 to reduce the activity and migration ability of HepG2 cells.

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  • 在线发布日期: 2022-11-21
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