miR⁃558靶向TNFAIP1调控肝癌的生长
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江苏高校优势学科建设工程资助项目(JX10231802)


miR⁃558 regulates the growth of liver cancer by targeting TNFAIP1
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    摘要:

    目的:探讨肝癌中微小RNA(microRNA,miR)-558的作用以及可能的相关分子机制。方法:采用RT-PCR检测miR-558在35对肝癌组织和癌旁组织中的表达。CCK-8、平板克隆和流式细胞仪检测miR-558和人肿瘤坏死因子-α诱导蛋白1(tumor necrosis factor-α induced protein 1,TNFAIP1)对肝癌细胞生长及周期的影响。荧光素酶报告实验研究miR-558与TNFAIP1的靶向关系。Western blot检测蛋白水平的表达变化。结果:miR-558在肝癌组织中的表达量明显高于癌旁组织(P < 0.01)。敲低miR-558可显著抑制肝癌细胞增殖,过表达miR-558可明显促进肝癌细胞生长(P < 0.01)。miR-558在肝癌细胞中直接靶向TNFAIP1抑制其表达发挥作用。上调TNFAIP1可显著消除miR-558对肝癌细胞的促进作用。结论:miR-558在肝癌组织中明显高表达,miR-558通过靶向调节TNFAIP1可明显促进肝癌细胞增殖。miR-558在肝癌患者中具有一定的靶向治疗价值。

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    Objective:To investigate the role and possible molecular mechanism of microRNA(miR)-558 in liver cancer. Methods:RT-PCR was used to detect the expression of miR-558 in 35 liver cancer tissues and 35 paracancerous tissues. The effects of miR-558 and TNFAIP1 on the growth and cycle of hepatoma cell were detected by cell counting kit-8(CCK-8),plate clone and flow cytometry. Luciferase assays were performed to analyze the relationship between miR-558 and TNFAIP1. The expression of protein level was detected by Western blot. Results:The expression of miR-558 in the liver cancer tissues was significantly higher than that in the paracancerous tissue(P < 0.01). Knock down of miR-558 significantly inhibited the proliferation of hepatoma cells,while overexpression of miR-558 could significantly promote the growth of hepatoma cells(P < 0.01). MiR-558 functioned in hepatoma cells through targeting TNFAIP1 directly. TNFAIP1 overexpression could significantly reverse the effect of miR-558 on hepatoma cell. Conclusion:MiR-558 was highly expressed in liver cancer tissue,and miR-558 can promote the proliferation of hepatoma cells by targeting TNFAIP1. MiR-558 had a certain value of target therapy in liver cancer patients.

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仲 晨,朱 勤. miR⁃558靶向TNFAIP1调控肝癌的生长[J].南京医科大学学报(自然科学版),2019,(8):1172-1176

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  • 收稿日期:2018-02-13
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  • 在线发布日期: 2019-08-29
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