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miR-196b靶向ERG促进肺腺癌的增殖和迁移

刘邦卿 李剑锋 刘晓辉 张劲男 梁金屏

刘邦卿, 李剑锋, 刘晓辉, 张劲男, 梁金屏. miR-196b靶向ERG促进肺腺癌的增殖和迁移[J]. 昆明医科大学学报, 2023, 44(10): 83-91. doi: 10.12259/j.issn.2095-610X.S20231023
引用本文: 刘邦卿, 李剑锋, 刘晓辉, 张劲男, 梁金屏. miR-196b靶向ERG促进肺腺癌的增殖和迁移[J]. 昆明医科大学学报, 2023, 44(10): 83-91. doi: 10.12259/j.issn.2095-610X.S20231023
Bangqing LIU, Jianfeng LI, Xiaohui LIU, Jinnan ZHANG, Jinping LIANG. MiR-196b Promotes Proliferation and Migration of Lung Adenocarcinoma by Targeting ERG[J]. Journal of Kunming Medical University, 2023, 44(10): 83-91. doi: 10.12259/j.issn.2095-610X.S20231023
Citation: Bangqing LIU, Jianfeng LI, Xiaohui LIU, Jinnan ZHANG, Jinping LIANG. MiR-196b Promotes Proliferation and Migration of Lung Adenocarcinoma by Targeting ERG[J]. Journal of Kunming Medical University, 2023, 44(10): 83-91. doi: 10.12259/j.issn.2095-610X.S20231023

miR-196b靶向ERG促进肺腺癌的增殖和迁移

doi: 10.12259/j.issn.2095-610X.S20231023
基金项目: 河北省医学科学研究课题基金资助项目(20231805)
详细信息
    作者简介:

    刘邦卿(1988~),男,山东巨野人,医学硕士,主治医师,主要从事肺癌基础与临床研究工作

  • 中图分类号: R734.2

MiR-196b Promotes Proliferation and Migration of Lung Adenocarcinoma by Targeting ERG

  • 摘要:   目的  探究miR-196b影响肺腺癌(lung adenocarcinoma,LUAD)进展的机制。  方法  通过TCGA数据库分析miR-196b在LUAD组织中的表达水平,利用TargetScan预测其下游靶基因并用双荧光素酶实验进行验证,qRT-PCR检测miR-196b和ETS相关基因(ETS-related gene,ERG)在LUAD细胞系中的表达情况,MTT、划痕愈合和Transwell实验分别检测不同处理后LUAD细胞的增殖、迁移和侵袭能力的变化情况。  结果  miR-196b在LUAD中高表达(P = 3.50e-17)并靶向负调控ERG,过表达miR-196b能够促进LUAD细胞的增殖、迁移和侵袭(P < 0.05),回复实验证实miR-196b/ERG调控轴能够影响LUAD细胞增殖、迁移和侵袭(P < 0.05)。  结论  miR-196b靶向ERG促进LUAD进展的分子机制,对开发LUAD新的临床治疗方法具有潜在意义。
  • 图  1  miR-196b和ERG在肺腺癌中的表达情况

    A:通过TCGA数据库预测miR-196b在正常组织和肺腺癌组织中的表达,绿框图表示正常样本(n = 46),红框图表示肿瘤样本(n = 521);B:肺腺癌患者miR-196b表达水平与总生存率的K-M分析,红色表示高表达组,蓝色表示低表达组;C:通过TCGA数据库预测正常组织和肺腺癌组织中ERG的表达,绿框图表示正常样本(n = 59),红框图表示肿瘤样本(n = 535)。

    Figure  1.  Expression of miR-196b and ERG in lung adenocarcinoma

    图  2  miR-196b在肺腺癌细胞中的表达情况

    与BEAS-2B组比较,*P < 0.05。

    Figure  2.  Expression of miR-196b in lung adenocarcinoma cells

    图  3  miR-196b可影响肺腺癌细胞的增殖、迁移和侵袭

    A:qRT-PCR检测过表达或敲低miR-196b后细胞的转染效率;B:MTT法检测过表达或敲低miR-196b后细胞的增殖能力;C:划痕愈合实验检测过表达或敲低miR-196b后细胞的迁移能力;D:Transwell实验检测过表达或敲低miR-196b后细胞的迁移和侵袭能力(100×)。与NC组比较,*P < 0.05。

    Figure  3.  miR-196b can affect the proliferation,migration and invasion of lung adenocarcinoma cells

    图  4  miR-196b的靶点检测及不同处理组细胞中ERG 的表达情况

    A:通过TargetScan数据库预测miR-196b和ERG的靶向结合位点;B:双荧光素酶法检测miR-196b与ERG的靶向结合关系;C:采用qRT-PCR和Western blot检测各细胞系中ERG mRNA和蛋白的表达;D:采用qRT-PCR和Western blot检测不同处理组ERG mRNA和蛋白的表达。与NC组或BEAS-2B组做比较,*P < 0.05。

    Figure  4.  Target detection of miR-196b and expression of ERG in cells of different treatment groups

    图  5  miR-196b能靶向下调ERG促进肺腺癌细胞的增殖、迁移和侵袭能力

    A:采用qRT-PCR和Western blot检测不同处理组大鼠ERG mRNA和蛋白的表达;B:MTT实验检测不同处理组的细胞增殖能力;C:划痕愈合实验检测不同处理组细胞迁移能力;D:Transwell实验检测不同处理组细胞的迁移和侵袭能力(100×)。NC-mimic、NC-inhibitor、oe-NC和si-NC分别表示miR-196b过表达、miR-196b沉默、ERG过表达和ERG沉默对照组,miR-mimic和miR-inhibitor分别表示miR-196b过表达和沉默组,oe-ERG和si-ERG分别表示ERG过表达组和沉默组;miR-mimic/inhibitor + oe/si-NC与NC组比较,miR-mimic/inhibitor + oe/si-NC组与miR-mimic/inhibitor + oe/si-ERG组比较,*P < 0.05,。

    Figure  5.  miR-196b can target down regulate ERG to promote the proliferation,migration and invasion of lung adenocarcinoma cells

    表  1  研究使用的细胞系及培养基

    Table  1.   Cell lines and media used in the study

    细胞系编号培养基
    BEAS-2B BNCC338205 DMEM-H
    PC-9 BNCC340767
    HCC-78 BNCC338064 RPMI-1640
    H1395 BNCC255519
    Calu-3 BNCC338514
    下载: 导出CSV

    表  2  引物序列表

    Table  2.   Primer Sequence Table

    基因引物序列(5′→ 3′)
    miR-196b Forward primer: GTACCACTTTATCCCGTTCACCA
    Reverse primer:ATCTCGAGGCAGGGAGAGAGGAATAA
    U6 Forward primer: GCCCATCTTGACCCGAAT
    Reverse primer: AACGCTTCACGAATTTGCGT
    ERG Forward primer:GAGTGGGCGGTGAAAGAATA
    Reverse primer: GGAGATGTGAGAGAAGAGTG
    GAPDH Forward primer:CTCCTCCTGTTCGACAGTCAGC
    Reverse primer:CCCAATACGACCAAATCCGTT
    下载: 导出CSV
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  • 收稿日期:  2023-06-26
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