MiR-15a-3p调节Twist1/Jagged1/Notch/KLF4信号通路对肺腺癌细胞增殖、凋亡、迁移和侵袭的影响

    Effects of miR-15a-3p on the proliferation, apoptosis, migration and invasion of lung adenocarcinoma cells by regulating Twist1/Jagged1/Notch/KLF4 signaling pathway

    • 摘要:
      目的 探讨miR-15a-3p通过调节碱性螺旋环螺旋转录因子1(Twist1)/Jagged1/Notch/Kruppel样因子4(KLF4)信号通路对肺腺癌细胞增殖、凋亡、迁移和侵袭的影响。
      方法 采用RT-qPCR实验检测肺腺癌组织、癌旁组织和肺腺癌细胞系(A549、HCC827)及人肺正常上皮细胞(BEAS-2B)中miR-15a-3p和Twist1 mRNA水平。A549细胞分成Control组(未转染)、NC mimics组(转染NC mimics)、miR-15a-3p mimics组(转染miR-15a-3p mimics)、si-NC组(转染si-NC)、si-Twist1组(转染si-Twist1)、miR-15a-3p mimics+pcDNA组(共转染miR-15a-3p mimics和pcDNA)、miR-15a-3p mimics+pc-Twist1组(共转染miR-15a-3p mimics和pc-Twist1)。CCK-8法检测细胞增殖情况;TUNEL凋亡试剂盒检测细胞凋亡情况;Transwell实验评估细胞迁移和侵袭能力;双荧光素酶报告分析实验确定miR-15a-3p和Twist1的靶向作用关系;Western blotting实验检测Twist1、Jagged1、Notch、KLF4蛋白表达水平。
      结果 在肺腺癌组织和细胞系中, miR-15a-3p表达降低, Twist1 mRNA表达升高(P < 0.05)。A549细胞通过转染miR-15a-3p mimics或si-Twist1, 上调miR-15a-3p或下调Twist1后, 细胞增殖率(24 h、48 h、72 h)显著下降, TUNEL阳性细胞比显著增加, 细胞迁移数和侵袭数显著降低(P < 0.05)。Twist1是miR-15a-3p的下游靶基因, 被miR-15a-3p直接负调控。Twist1的上调明显逆转了miR-15a-3p过表达对A549细胞进展的抑制作用。miR-15a-3p过表达抑制Jagged1、Notch、KLF4蛋白表达, 而继续上调表达Twist1后Jagged1、Notch、KLF4蛋白表达明显升高(P < 0.05)。
      结论 miR-15a-3p通过靶向抑制Twist1/Jagged1/Notch/KLF4信号通路, 降低A549细胞增殖、迁移和侵袭能力, 促进凋亡。

       

      Abstract:
      Objective To investigate the effects of miR-15a-3p on the proliferation, apoptosis, migration and invasion of lung adenocarcinoma cells by regulating Twist basic helix-loop-helix transcription factor 1 (Twist1)/Jagged1/Notch/Kruppel-like factor 4 (KLF4) signaling pathway.
      Methods The miR-15a-3p and Twist1 mRNA levels in lung adenocarcinoma tissues, adjacent tissues, lung adenocarcinoma cells lines (A549, HCC827) and human lung normal epithelial cells (BEAS-2B) were measured through RT-qPCR.A549 cells were divided into control group (untransfected), NC mimics group (transfected with NC mimics), miR-15a-3p mimics group (transfected with miR-15a-3p mimics), si-NC group (transfected with si-NC), si-Twist1 group (transfected with si-Twist1), miR-15a-3p mimics+pcDNA group (co-transfected with miR-15a-3p mimics and pcDNA), and miR-15a-3p mimics+pc-Twist1 group (co-transfected with miR-15a-3p mimics and pc-Twist1).Cell proliferation was measured using CCK-8 assay, apoptosis was measured through TUNEL apoptosis kit, cell migration and invasion abilities were evaluated by Transwell assay, the targeting relationship between miR-15a-3p and Twist1 was measured through dual luciferase reporter assay, and the protein expression levels of Twist1, Jagged1, Notch and KLF4 were examined by Western blotting.
      Results In lung adenocarcinoma tissues and cell lines, miR-15a-3p expression was decreased, and Twist1 mRNA level was increased (P < 0.05).After A549 cells were transfected with miR-15a-3p mimics or si-Twist1 to up-regulate miR-15a-3p or down-regulate Twist1, the cell proliferation rates at 24 h, 48 h and 72 h were significantly decreased, and the ratio of TUNEL-positive cells was significantly increased, the numbers of cell migration and invasion were significantly decreased (P < 0.05).Twist1 was a downstream target gene of miR-15a-3p, and was directly negative-regulated by miR-15a-3p.Upregulation of Twist1 significantly reversed the inhibitory effect of miR-15a-3p overexpression on A549 cell progression.Overexpression of miR-15a-3p inhibited the expression of Jagged1, Notch, and KLF4, while the expression of Jagged1, Notch, and KLF4 were increased significantly after up-regulation of Twist1 (P < 0.05).
      Conclusions MiR-15a-3p can target and inhibit the Twist1/Jagged1/Notch/KLF4 signaling pathway to reduce the proliferation, migration and invasion abilities and promote apoptosis of A549 cells.

       

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