首页> 美国卫生研究院文献>World Journal of Gastroenterology >Mitotic cell death in BEL-7402 cells induced by enediyne antibiotic lidamycin is associated with centrosome overduplication
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Mitotic cell death in BEL-7402 cells induced by enediyne antibiotic lidamycin is associated with centrosome overduplication

机译:烯二炔抗生素利达霉素诱导的BEL-7402细胞有丝分裂细胞死亡与中心体过度复制有关

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摘要

AIM: Mitotic cell death has been focused on in tumor therapy. However, the precise mechanisms underlying it remain unclear. We have reported previously that enediyne antibiotic lidamycin induces mitotic cell death at low concentrations in human epithelial tumor cells. The aim of this study was to investigate the possible link between centrosome dynamics and lidamycin-induced mitotic cell death in human hepatoma BEL-7402 cells.METHODS: Growth curve was established by MTT assay. Cell multinucleation was detected by staining with Hoechst 33342. Flow cytometry was used to analyze cell cycle. Aberrant centrosomes were detected by indirect immunofluorescence. Western blot and senescence-associated β-galactosidase (SA-β-gal) staining were used to analyze protein expression and senescence-like phenotype, respectively.RESULTS: Exposure of BEL-7402 cells to a low concentration of lidamycin resulted in an increase in cells containing multiple centrosomes in association with the appearance of mitotic cell death and activation of SA-β-gal in some cells, accompanied by the changes of protein expression for the regulation of proliferation and apoptosis. The mitochondrial signaling pathway, one of the major apoptotic pathways, was not activated during mitotic cell death. The aberrant centrosomes contributed to the multipolar mitotic spindles formation, which might lead to an unbalanced division of chromosomes and mitotic cell death characterized by the manifestation of multi- or micronucleated giant cells. Cell cycle analysis revealed that the lidamycin treatment provoked the retardation at G2/M phase, which might be involved in the centrosome overduplication.CONCLUSION: Mitotic cell death and senescence can be induced by treatment of BEL-7402 cells with a low concentration of lidamycin. Centrosome dysregulation may play a critical role in mitotic failure and ultimate cell death following exposure to intermediate dose of lidamycin.
机译:目的:有丝分裂细胞死亡已集中在肿瘤治疗上。但是,其背后的确切机制仍不清楚。以前我们曾报道过,烯二炔抗生素利达霉素在人上皮肿瘤细胞中低浓度时可诱导有丝分裂细胞死亡。本研究的目的是研究人肝癌BEL-7402细胞中中心体动力学与利达霉素诱导的有丝分裂细胞死亡之间的可能联系。方法:MTT法建立生长曲线。通过用Hoechst 33342染色检测细胞多核化。使用流式细胞仪分析细胞周期。通过间接免疫荧光检测异常中心体。结果:将BEL-7402细胞暴露于低浓度的利达霉素时,蛋白质表达和衰老样表型分别用于蛋白质表达和衰老样表型的分析。结果:含有多个中心体的细胞与某些细胞中有丝分裂细胞死亡的出现和SA-β-gal的活化有关,并伴随着蛋白质表达的变化,以调节增殖和凋亡。线粒体信号传导途径是主要的凋亡途径之一,在有丝分裂细胞死亡过程中未被激活。异常的中心体促成多极有丝分裂纺锤体的形成,这可能导致染色体的不平衡分裂和以多核或微核巨细胞的表现为特征的有丝分裂细胞死亡。细胞周期分析表明,利达霉素处理引起了G2 / M期的阻滞,这可能与中心体的过度复制有关。结论:低剂量的利达霉素处理BEL-7402细胞可以诱导有丝分裂细胞的死亡和衰老。暴露于中等剂量的利达霉素后,中心体失调可能在有丝分裂失败和最终细胞死亡中起关键作用。

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