Faculty of Pharmaceutical Sciences, Sojo University, 4-22-1 Ikeda, Nishi-ku, Kumamoto, 860-0082, Japan.
Histochem Cell Biol. 2021 Nov;156(5):409-421. doi: 10.1007/s00418-021-02020-w. Epub 2021 Jul 31.
Elevated expression of the nucleoporin Nup88, a constituent of the nuclear pore complex, is seen in various types of malignant tumors, but whether this overexpression contributes to the malignant phenotype has yet to be determined. Here, we investigated the effect of the overexpression of Nup88 on the migration and invasion of cervical cancer HeLa cells. The overexpression of Nup88 promoted a slight but significant increase in both migration and invasion, whereas knockdown of Nup88 by RNA interference suppressed these phenotypes. The observed phenotypes in Nup88-overexpressing HeLa cells were not due to the progression of the epithelial-to-mesenchymal transition or activation of NF-κB, which are known to be important for cell migration and invasion. Instead, we identified an upregulation of matrix metalloproteinase-12 (MMP-12) at both the gene and protein levels in Nup88-overexpressing HeLa cells. Upregulation of MMP-12 protein by the overexpression of Nup88 was also observed in one other cervical cancer cell line and two prostate cancer cell lines but not 293 cells. Treatment with a selective inhibitor against MMP-12 enzymatic activity significantly suppressed the invasive ability of HeLa cells induced by Nup88 overexpression. Taken together, our results suggest that overexpression of Nup88 can stimulate malignant phenotypes including invasive ability, which is promoted by MMP-12 expression.
核孔复合体的组成部分核孔蛋白 Nup88 的表达水平在各种类型的恶性肿瘤中升高,但这种过表达是否有助于恶性表型尚待确定。在这里,我们研究了 Nup88 过表达对宫颈癌 HeLa 细胞迁移和侵袭的影响。Nup88 的过表达促进了迁移和侵袭的轻微但显著增加,而 RNA 干扰敲低 Nup88 则抑制了这些表型。在 Nup88 过表达的 HeLa 细胞中观察到的表型不是由于上皮间质转化的进展或 NF-κB 的激活,已知这对于细胞迁移和侵袭很重要。相反,我们在 Nup88 过表达的 HeLa 细胞中鉴定出基质金属蛋白酶 12(MMP-12)在基因和蛋白水平上的上调。在另一个宫颈癌细胞系和两个前列腺癌细胞系中观察到 Nup88 过表达导致 MMP-12 蛋白的上调,但在 293 细胞中没有观察到。用针对 MMP-12 酶活性的选择性抑制剂处理可显著抑制 Nup88 过表达诱导的 HeLa 细胞的侵袭能力。总之,我们的结果表明,Nup88 的过表达可以刺激包括侵袭能力在内的恶性表型,这是由 MMP-12 表达促进的。