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Downregulation of NOP53 Ribosome Biogenesis Factor Leads to Abnormal Nuclear Division and Chromosomal Instability in Human Cervical Cancer Cells

机译:NOP53核糖体生物发生因子的下调导致人宫颈癌细胞异常核划分和染色体不稳定性

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摘要

NOP53 ribosome biogenesis factor (NOP53) is a nucleolar protein involved in oncogenesis/tumor suppression, cell cycle regulation, and cell death. Here, we investigated the role of NOP53 in the maintenance of normal nuclear shape and chromosomal stability. Depletion of NOP53 by shRNA caused abnormal nuclear morphology, including large nucleus, irregular nucleus, and multinucleated cells, and chromosomal instability resulting in micronucleus or nuclear bud formation. The abnormal nuclear shape and chromosomal instability were restored by re-expression of NOP53. We further showed that NOP53 was involved in chromosome congression in metaphase. Downregulation of NOP53 induced aberrant chromosome congression and spindle checkpoint activation, resulting in delayed mitosis and mitotic arrest. Thus, our findings demonstrated that the nucleolar protein NOP53 participated in mitotic progression and that dysregulated NOP53 expression caused chromosomal instability in cancer cells.
机译:NOP53核糖体生物发生因子(NOP53)是癌症/肿瘤抑制,细胞周期调节和细胞死亡中的核仁蛋白。 在这里,我们研究了NOP53在维持正常核形状和染色体稳定性中的作用。 通过shRNA的NOP53耗尽导致核形态异常,包括大核,不规则核和多核细胞,以及导致微核或核芽形成的染色体不稳定性。 通过再表达NOP53来恢复异常的核形状和染色体不稳定性。 我们进一步表明,NOP53参与了中期中的染色体会议。 下调NOP53诱导异常染色体会非和主轴检查点激活,导致有丝分裂和有丝分裂的延迟。 因此,我们的研究结果表明,核仁蛋白NOP53参与了有丝分裂进展,并且具有疑虑的NOP53表达引起癌细胞中的染色体不稳定性。

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