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首页> 外文期刊>Molecules >Parthenolide Induces Apoptosis and Cell Cycle Arrest of Human 5637 Bladder Cancer Cells In Vitro
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Parthenolide Induces Apoptosis and Cell Cycle Arrest of Human 5637 Bladder Cancer Cells In Vitro

机译:爬山酚内酯可诱导人5637膀胱癌细胞凋亡和细胞周期阻滞

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摘要

Parthenolide, the principal component of sesquiterpene lactones present in medical plants such as feverfew (Tanacetum parthenium), has been reported to have anti-tumor activity. In this study, we evaluated the therapeutic potential of parthenolide against bladder cancer and its mechanism of action. Treatment of bladder cancer cells with parthenolide resulted in a significant decrease in cell viability. Parthenolide induced apoptosis through the modulation of Bcl-2 family proteins and poly (ADP-ribose) polymerase degradation. Treatment with parthenolide led to G1 phase cell cycle arrest in 5637 cells by modulation of cyclin D1 and phosphorylated cyclin-dependent kinase 2. Parthenolide also inhibited the invasive ability of bladder cancer cells. These findings suggest that parthenolide could be a novel therapeutic agent for treatment of bladder cancer.
机译:据报道,存在于药用植物中的倍半萜内酯的主要成分,例如小白菊(艾菊(Tanacetum parthenium))具有抗肿瘤活性。在这项研究中,我们评估了小白菊内酯对膀胱癌的治疗潜力及其作用机理。用小白菊内酯处理膀胱癌细胞导致细胞活力显着下降。偏苯二酚通过调节Bcl-2家族蛋白和聚(ADP-核糖)聚合酶降解诱导细胞凋亡。单性酚的治疗通过调节细胞周期蛋白D1和磷酸化的细胞周期蛋白依赖性激酶2导致5637个细胞中的G1期细胞周期停滞。单性酚也抑制膀胱癌细胞的侵袭能力。这些发现表明,小白菊内酯可能是治疗膀胱癌的新型治疗剂。

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