汪景坤, 樊丽伟, 李洵, 付晓霞, 赵彦焕, 张东姣, 赵玉红, 张磊. circ_0000515靶向miR-1258调控结肠癌细胞增殖和凋亡的机制研究[J]. 蚌埠医科大学学报, 2021, 46(12): 1649-1653. DOI: 10.13898/j.cnki.issn.1000-2200.2021.12.002
    引用本文: 汪景坤, 樊丽伟, 李洵, 付晓霞, 赵彦焕, 张东姣, 赵玉红, 张磊. circ_0000515靶向miR-1258调控结肠癌细胞增殖和凋亡的机制研究[J]. 蚌埠医科大学学报, 2021, 46(12): 1649-1653. DOI: 10.13898/j.cnki.issn.1000-2200.2021.12.002
    WANG Jing-kun, FAN Li-wei, LI Xun, FU Xiao-xia, ZHAO Yan-huan, ZHANG Dong-jiao, ZHAO Yu-hong, ZHANG Lei. Effect of circ_0000515 targeting miR-1258 on the proliferation and apoptosis in the colon cancer cells[J]. Journal of Bengbu Medical University, 2021, 46(12): 1649-1653. DOI: 10.13898/j.cnki.issn.1000-2200.2021.12.002
    Citation: WANG Jing-kun, FAN Li-wei, LI Xun, FU Xiao-xia, ZHAO Yan-huan, ZHANG Dong-jiao, ZHAO Yu-hong, ZHANG Lei. Effect of circ_0000515 targeting miR-1258 on the proliferation and apoptosis in the colon cancer cells[J]. Journal of Bengbu Medical University, 2021, 46(12): 1649-1653. DOI: 10.13898/j.cnki.issn.1000-2200.2021.12.002

    circ_0000515靶向miR-1258调控结肠癌细胞增殖和凋亡的机制研究

    Effect of circ_0000515 targeting miR-1258 on the proliferation and apoptosis in the colon cancer cells

    • 摘要:
      目的探讨circ_0000515调控结肠癌细胞增殖和凋亡的分子机制。
      方法选取41例结肠癌病人癌组织及癌旁组织标本,用实时荧光定量PCR(RT-qPCR)检测circ_0000515和miR-1258的表达水平;结肠癌细胞SW620分为si-circ_0000515组、si-NC组、miR-1258组、miR-NC组、si-circ_0000515+anti-miR-NC组、si-circ_0000515+anti-miR-1258组。四甲基偶氮唑盐比色法(MTT)检测SW620细胞活性;流式细胞术检测SW620细胞凋亡;双荧光素酶报告实验检测circ_0000515和miR-1258的靶向关系。
      结果与癌旁组织比较,结肠癌组织中circ_0000515表达水平升高,miR-1258表达水平降低(P < 0.01)。抑制circ_0000515表达或过表达miR-1258,SW620细胞活性降低,SW620细胞的凋亡率升高(P < 0.01)。circ_0000515靶向调控miR-1258;干扰miR-1258表达逆转了抑制circ_0000515表达对结肠癌SW620细胞增殖和凋亡的作用。
      结论抑制circ_0000515表达通过靶向上调miR-1258抑制结肠癌细胞增殖,促进凋亡。

       

      Abstract:
      ObjectiveTo explore the molecular mechanism of circ_0000515 regulating the proliferation and apoptosis of colon cancer cells.
      MethodsA total of 41 cases of colon cancer patients with cancer tissue and adjacent tissue samples were selected.Real-time fluorescent quantitative PCR was used to detect the expression of circ_0000515 and miR-1258.Colon cancer cells SW620 were divided into si-circ_0000515 group, si-NC group, miR-1258 group, miR-NC group, si-circ_0000515+anti-miR-NC group, si-circ_0000515+anti-miR-1258 group.Tetramethylazolium salt colorimetric assay(MTT) was used to detect the cell viability.Flow cytometry was used to detect apoptosis.The targeting relationship of circ_0000515 and miR-1258 was detected by dual-luciferase reporter assay.
      ResultsCompared with the adjacent tissues, the expression of circ_0000515 in colon cancer tissues was increased, and the expression of miR-1258 was decreased(P < 0.01).After the inhibition of circ_0000515 expression or overexpression of miR-1258, the viability of SW620 cells was decreased, the apoptosis rate was increased(P < 0.01).Circ_0000515 targeted and regulated the expression of miR-1258.Interference with miR-1258 expression reversed the effect of inhibiting circ_0000515 expression on the proliferation and apoptosis of colon cancer SW620 cells.
      ConclusionsInhibiting the expression of circ_0000515 by up-regulation of miR-1258 can inhibit the proliferation and promote the apoptosis in colon cancer cells.

       

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