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JNK Inactivation Induces Polyploidy and Drug-Resistance in Coronarin D-Treated Osteosarcoma Cells

机译:JNK灭活诱导Coronarin D处理的骨肉瘤细胞中的多倍性和耐药性。

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摘要

Inhibition of proliferating cells is a critical strategy for cancer therapy. In this study, we demonstrated that coronarin D, a natural component extracted from the rhizomes of Hedychium coronarium, significantly suppressed the proliferation of osteosarcoma cells. The treatment with coronarin D resulted in the activation of caspase-3 and apoptosis. This treatment induced the accumulation of cyclin B1 and DNA condensation indicating the treated osteosarcoma cells were arrested in mitotic phase. Furthermore, the treatment with coronarin D increased the levels of phosphorylated c-Jun NH2-terminal kinase (JNK) in human osteosarcoma cells. Pretreatment with JNK inhibitor blocked the accumulation of cyclin B1 and DNA condensation, resulting the accumulation of tetraploid cells in coronarin D-treated osteosarcoma HOS cells, indicating JNK inactivation blocked the mitotic entry and arrested cells in the 4 N state. After adaptation, the arrested tetraploid cells continued to duplicate their DNA resulting in polyploidy. Interestingly, when the arrested mitotic cells induced by coronarin D were treated with JNK inhibitor, the accumulated cyclin B1 and DNA condensation were immediately eliminated. These arrested 4 N cells loss the ability to undergo cytokinesis, and ultimately continued to duplicate DNA upon prolonged arrest resulting in the production of polyploid populations. JNK inactivation, either by the pretreatment with JNK inhibitor or the treatment with JNK inhibitor in coronarin D-induced mitotic cells, both caused resistance to coronarin D-induced cell death. Taken together, our findings indicate that coronarin D induces the apoptosis and mitosis arrest in human osteosarcoma cells. JNK has a crucial role in coronarin D-induced mitosis arrest and apoptosis. We hypothesize that functional evaluation of JNK may produce more specific and effective therapies in coronarin D-related trail for treatment of human osteosarcoma.
机译:抑制增殖细胞是癌症治疗的关键策略。在这项研究中,我们证明了冠状花冠素D是从Hedychium coronarium的根茎中提取的天然成分,可显着抑制骨肉瘤细胞的增殖。用Coronarin D处理导致caspase-3活化和凋亡。这种处理诱导了细胞周期蛋白B1的积累和DNA缩合,表明处理过的骨肉瘤细胞被阻滞在有丝分裂期。此外,用Coronarin D处理可增加人骨肉瘤细胞中磷酸化的c-Jun NH2-末端激酶(JNK)的水平。用JNK抑制剂预处理可阻断细胞周期蛋白B1的积累和DNA缩合,从而导致四倍体细胞在经冠冕蛋白D处理的骨肉瘤HOS细胞中积累,表明JNK失活阻止了有丝分裂进入,并使细胞停滞在4 N状态。适应后,被捕的四倍体细胞继续复制其DNA,从而产生多倍体。有趣的是,当用JNK抑制剂处理冠状病毒D诱导的停滞的有丝分裂细胞时,立即消除了积累的细胞周期蛋白B1和DNA缩合。这些被捕的4 N细胞失去了进行胞质分裂的能力,并在长时间的捕杀中最终继续复制DNA,从而导致多倍体种群的产生。在Coronarin D诱导的有丝分裂细胞中,通过用JNK抑制剂预处理或通过JNK抑制剂处理而使JNK失活均引起对Coronarin D诱导的细胞死亡的抗性。两者合计,我们的发现表明,冠状病毒D诱导人骨肉瘤细胞凋亡和有丝分裂停滞。 JNK在冠状病毒D诱导的有丝分裂阻滞和凋亡中具有关键作用。我们假设JNK的功能评估可能会在冠状病毒D相关的线索中产生更特异性和有效的疗法来治疗人骨肉瘤。

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