CircASAP1靶向miR-4500促进骨肉瘤细胞增殖并抑制凋亡的机制研究

Mechanism study on circASAP1 promoting proliferationand inhibiting apoptosis of osteosarcoma cells by targeting miR-4500

  • 摘要:
    目的 探讨环状RNA ASAP1(circASAP1)靶向微小RNA-4500(miR-4500)对骨肉瘤细胞增殖和凋亡的调控作用。
    方法 选取人成骨肉瘤细胞(Saos-2)作为实验对象,将其置于含有10%胎牛血清的DMEM培养基中培养,同时维持5%的CO2。采用RT-qPCR检测circASAP1和miR-4500在骨肉瘤组织中的表达。分别转染si-NC(40 nmol/L)、si-circASAP1(40 nmol/L)、pcDNA(0.4 μg)、pcDNA-circASAP1(0.4 μg)、miR-NC(40 nmol/L)、miR-4500模拟物(40 nmol/L)、si-circASAP1+anti-miR-NC(40 nmol/L)、si-circASAP1+anti-miR-4500(40 nmol/L)至Saos-2细胞。采用CCK-8、集落形成实验、流式细胞术检测细胞增殖和凋亡。采用双荧光素酶报告实验分析circASAP1与miR-4500的相互作用。
    结果 相较于瘤旁组织,骨肉瘤组织中circASAP1表达升高, miR-4500表达降低,差异均有统计学意义(P < 0.001)。与si-NC组比较, si-circASAP1组circASAP1表达、吸光度(OD)值、细胞克隆形成数降低,差异均有统计学意义(P < 0.001)。与si-NC组比较,si-circASAP1组cleaved-caspase3蛋白水平、cleaved-caspase9蛋白水平、凋亡率上调,差异均有统计学意义(P < 0.001)。StarBase搜索发现miR-4500与circASAP1存在特异性结合序列。miR-4500模拟物和WT-circASAP1共转染显著降低细胞的相对荧光素酶活性(0.34±0.03)与(0.95±0.06), t=27.280, P < 0.001。pcDNA-circASAP1组miR-4500表达低于pcDNA组,而si-circASAP1组miR-4500表达高于si-NC组,差异均有统计学意义(P < 0.001)。与miR-NC组比较,miR-4500组miR-4500表达、cleaved-caspase3蛋白水平、cleaved-caspase9蛋白水平、凋亡率升高,而OD值、克隆形成数下降,差异均有统计学意义(P < 0.001)。与si-circASAP1+anti-miR-NC组比较,si-circASAP1+anti-miR-4500组miR-4500表达、cleaved-caspase3蛋白水平、cleaved-caspase9蛋白水平、凋亡率下降,而OD值、克隆形成数上调,差异均有统计学意义(P < 0.001)。
    结论 骨肉瘤组织中circASAP1表达增加, miR-4500表达降低,且circASAP1通过靶向miR-4500促进骨肉瘤细胞增殖并抑制凋亡。

     

    Abstract:
    Objective To investigate the regulatory effect of circular RNA ASAP1 (circASAP1) targeting microRNA-4500 (miR-4500) on the proliferation and apoptosis of osteosarcoma cells.
    Methods Human osteosarcoma cells (Saos-2) were selected as the experimental subjects and cultured in DMEM medium containing 10% fetal bovine serum while maintaining 5% CO2. The expressions of circASAP1 and miR-4500 in osteosarcoma tissues were detected using RT-qPCR. Saos-2 cells were transfected with si-NC (40 nmol/L), si-circASAP1 (40 nmol/L), pcDNA (0.4 μg), pcDNA-circASAP1 (0.4 μg), miR-NC (40 nmol/L), miR-4500 mimics (40 nmol/L), si-circASAP1+anti-miR-NC (40 nmol/L), and si-circASAP1+anti-miR-4500 (40 nmol/L), respectively. Cell proliferation and apoptosis were assessed using CCK-8, colony formation assays, and flow cytometry. The interaction between circASAP1 and miR-4500 was analyzed using a dual-luciferase reporter assay.
    Results Compared with adjacent non-tumor tissues, the expression of circASAP1 was significantly upregulated, while that of miR-4500 was significantly downregulated in osteosarcoma tissues (P < 0.001). Compared with the si-NC group, the si-circASAP1 group exhibited significantly decreased circASAP1 expression, optical density (OD) values, and the number of cell colonies (P < 0.001). Compared with the si-NC group, the si-circASAP1 group showed significantly upregulated levels of cleaved-caspase3 protein, cleaved-caspase9 protein, and the apoptosis rate (P < 0.001). StarBase search revealed specific binding sequences between miR-4500 and circASAP1. Co-transfection of miR-4500 mimics and WT-circASAP1 significantly reduced the relative luciferase activity of the cells(0.34±0.03) versus (0.95±0.06), t=27.280, P < 0.001. The expression of miR-4500 in the pcDNA-circASAP1 group was significantly lower than that in the pcDNA group, whereas the expression of miR-4500 in the si-circASAP1 group was significantly higher than that in the si-NC group (P < 0.001). Compared with the miR-NC group, the miR-4500 group exhibited significantly increased miR-4500 expression, cleaved-caspase3 protein levels, cleaved-caspase9 protein levels, and the apoptosis rate, while the OD values and the number of colonies significantly decreased (P < 0.001). Compared with the si-circASAP1+anti-miR-NC group, the si-circASAP1+anti-miR-4500 group showed significantly decreased miR-4500 expression, cleaved-caspase3 protein levels, cleaved-caspase9 protein levels, and the apoptosis rate, while the OD values and the number of colonies significantly increased (P < 0.001).
    Conclusion The expression of circASAP1 is increased, while that of miR-4500 is decreased in osteosarcoma tissues. Moreover, circASAP1 promotes the proliferation and inhibits the apoptosis of osteosarcoma cells by targeting miR-4500.

     

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