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宫颈癌细胞中ΔNp63α对白血病抑制因子表达水平的影响及其机制

Effect ofΔNp63αon Leukemia Inhibitory Factor Expression in Cervical Cancer Cells and Related Mechanism

  • 摘要:
    目的 探讨ΔNp63α对白血病抑制因子表达水平的影响及其机制。
    方法 通过稳定转染构建稳定过表达ΔNp63α的SiHa细胞株(SiHa/ΔNp63α);通过瞬时转染沉默ME-180细胞中ΔNp63α的表达水平;并通过Western blot检测两组细胞中ΔNp63α、LIF、STAT3的蛋白水平,通过qRT-PCR检测两组细胞中ΔNp63α、LIF、STAT3、LncRNA ENST00000447565的转录水平。
    结果 (1)ΔNp63α过表达的SiHa细胞中,LIF的mRNA及蛋白水平均明显下调,其调控的下游基因STAT3的mRNA表达水平也显著下降;(2)ΔNp63α过表达的SiHa细胞中,LncRNA ENST00000447565的转录水平显著下调,该LncRNA与LIF基因均在22号染色体q12.2,且基因组位置接近;(3)ΔNp63α沉默的ME-180细胞中,LIF的表达量明显上调。
    结论 ΔNp63α可以抑制LIF及下游基因STAT3的表达水平,其机制可能与ΔNp63α对LncRNA ENST00000447565的表达抑制有关。

     

    Abstract:
    Objective To explore the effect ofΔNp63αon the expression level of leukemia inhibitory factor (LIF) and its mechanism.
    Methods Stable SiHa cells with overexpressedΔNp63α(SiHa/ΔNp63α) were established by stable transfection, andΔNp63αexpression was transiently silenced in ME-180 cell lines(ME-180/ΔNp63αsiRNA). The protein levels ofΔNp63α, LIF and STAT3 were detected by Western blot, while the mRNA levels ofΔNp63α, LIF, STAT3 and LncRNA ENST00000447565 were detected by qRT-PCR.
    Results (1) The mRNA and protein levels of LIF and its downstream signaling factor STAT3 mRNA was significantly reduced in SiHa/ΔNp63αcells; (2) The RNA levels of LncRNA ENST00000447565 were significantly reduced in SiHa/ΔNp63αcells, ENST00000447565 and LIF were both located in chromosome 22 q12.2, within the same loci; (3) The mRNA level of LIF was significantly increased in ME-180 cells with silencedΔNp63α.
    Conclusion The expressions of LIF and its downstream signaling factor STAT3 are inhibited byΔNp63αexpression, which might be associated with the down-regulation of LncRNA ENST00000447565.

     

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