首页> 外文期刊>Archives of pharmacal research >Butein sensitizes human leukemia cells to apoptosis induced by tumor necrosis factor-related apoptosis inducing ligand (TRAIL).
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Butein sensitizes human leukemia cells to apoptosis induced by tumor necrosis factor-related apoptosis inducing ligand (TRAIL).

机译:Butein使人白血病细胞对肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的凋亡敏感。

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摘要

Resistance to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) therapy is frequently encountered, requiring combined treatments with sensitizing agents. It is, therefore, important to find nontoxic drugs which can be used together with TRAIL. In this study, we investigated natural compounds that can overcome resistance to TRAIL, and found that butein, a polyphenol, exhibits significant synergism with TRAIL. Treatment with TRAIL in combination with subtoxic concentrations of butein sensitizes TRAIL-resistant human leukemia U937 cells to apoptosis. Butein increased caspase-3 activity and expression of death receptor DR5. The apoptotic cell death induced by combined treatment was significantly reduced by z-DEVD-fmk, a caspase-3 inhibitor, suggesting a critical role of caspase-3 in apoptosis. These results indicate that butein sensitizes TRAIL-resistant U937 cells to TRAIL-induced apoptosis in a caspase-3 dependent manner which might be correlated with upregulation of death receptor DR5. Ourdata suggests that combined treatment with butein and TRAIL may provide a safe and effective strategy for treating cancer.
机译:经常遇到对肿瘤坏死因子相关的凋亡诱导配体(TRAIL)治疗的耐药性,需要与敏化剂联合治疗。因此,重要的是找到可以与TRAIL一起使用的无毒药物。在这项研究中,我们研究了可以克服对TRAIL耐药性的天然化合物,发现多酚丁烯酸酯与TRAIL具有明显的协同作用。 TRAIL联合亚毒性浓度的丁烯酸处理可使TRAIL抗性人白血病U937细胞对细胞凋亡敏感。 Butein增加caspase-3活性和死亡受体DR5的表达。 caspase-3抑制剂z-DEVD-fmk显着降低了联合治疗诱导的凋亡细胞死亡,表明caspase-3在凋亡中起关键作用。这些结果表明酪蛋白以caspase-3依赖性方式使TRAIL抗性U937细胞对TRAIL诱导的凋亡敏感,这可能与死亡受体DR5的上调有关。我们的数据表明,丁酸和TRAIL联合治疗可能为治疗癌症提供安全有效的策略。

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