首页> 外文期刊>Nutrition and Cancer: An International Journal >Ayurvedic medicine constituent withaferin a causes G2 and M phase cell cycle arrest in human breast cancer cells.
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Ayurvedic medicine constituent withaferin a causes G2 and M phase cell cycle arrest in human breast cancer cells.

机译:阿育吠陀药物成分aferin a导致人乳腺癌细胞中的G2和M期细胞周期停滞。

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摘要

Withaferin A (WA) is derived from the medicinal plant Withania somnifera that has been safely used for centuries in the Indian Ayurvedic medicine for treatment of various ailments. We now demonstrate that WA treatment causes G2 and mitotic arrest in human breast cancer cells. Treatment of MDA-MB-231 (estrogen-independent) and MCF-7 (estrogen-responsive) cell lines with WA resulted in a concentration- and time-dependent increase in G2-M fraction, which correlated with a decrease in levels of cyclin-dependent kinase 1 (Cdk1), cell division cycle 25C (Cdc25C) and/or Cdc25B proteins, leading to accumulation of Tyrosine15 phosphorylated (inactive) Cdk1. Ectopic expression of Cdc25C conferred partial yet significant protection against WA-mediated G2-M phase cell cycle arrest in MDA-MB-231 cells. The WA-treated MDA-MB-231 and MCF-7 cells were also arrested in mitosis as judged by fluorescence microscopy and analysis of Ser10 phosphorylated histone H3. Mitotic arrest resulting from exposure to WA was accompanied by an increase in the protein level of anaphase promoting complex/cyclosome substrate securin. In conclusion, the results of this study suggest that G2-M phase cell cycle arrest may be an important mechanism in antiproliferative effect of WA against human breast cancer cells.
机译:Withaferin A(WA)来源于药用植物Withania somnifera,在印度阿育吠陀医学中已安全使用了多个世纪,用于治疗各种疾病。现在我们证明WA治疗可导致人乳腺癌细胞中的G2和有丝分裂停滞。用WA处理MDA-MB-231(非雌激素依赖性)和MCF-7(雌激素响应)细胞系会导致G2-M分数的浓度和时间依赖性增加,这与细胞周期蛋白水平的降低有关依赖性激酶1(Cdk1),细胞分裂周期25C(Cdc25C)和/或Cdc25B蛋白,导致酪氨酸15磷酸化(无活性)Cdk1积累。 Cdc25C的异位表达为MDA-MB-231细胞中WA介导的G2-M期细胞周期停滞提供了部分但重要的保护。通过荧光显微镜和Ser10磷酸化组蛋白H3的分析判断,经WA处理的MDA-MB-231和MCF-7细胞也被阻滞在有丝分裂中。暴露于WA引起的有丝分裂停滞伴随着后期促进复合物/环体底物securin的蛋白质水平的增加。总之,这项研究的结果表明,G2-M期细胞周期停滞可能是WA对人乳腺癌细胞的抗增殖作用的重要机制。

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