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首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >Curcumin induces apoptosis in lung cancer cells by 14-3-3 protein-mediated activation of Bad
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Curcumin induces apoptosis in lung cancer cells by 14-3-3 protein-mediated activation of Bad

机译:姜黄素在14-3-3蛋白介导的坏的激活诱导肺癌细胞凋亡

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摘要

The anticancer effects of curcumin are based on the induction of apoptosis, but the specific mechanisms have not yet been fully elucidated. To address this issue, we investigated the effects of curcumin on the intrinsic apoptosis pathway using mitochondria from A549 cells. Curcumin decreased the levels of 14-3-3 proteins, key molecules that inhibit the activation of proapoptotic factors known as BH3-only proteins (e.g. Bad). Curcumin-induced suppression of 14-3-3 protein levels was associated with reduced cytosolic Bad and elevation of mitochondrial Bad, leading to a drop in the mitochondrial membrane potential. 14-3-3 proteins generally interact with Bad phosphorylated by AKT, thus preventing its translocation to the mitochondria where it can promote cell death. Curcumin not only decreased the expression of 14-3-3 proteins but also promoted Bad dephosphorylation in an AKT-dependent fashion. Our results provide novel evidence for the induction of apoptosis by curcumin at multiple stages of the mitochondrial cascade.
机译:姜黄素的抗癌效果基于凋亡的诱导,但尚未完全阐明特定机制。为了解决这个问题,我们研究了姜黄素对来自A549细胞线粒体的内在凋亡途径的影响。姜黄素降低了14-3-3蛋白的水平,抑制称为BH3蛋白(例如坏)的凋亡因子激活的关键分子。姜黄素诱导的抑制14-3-3蛋白水平与细胞溶质损伤和线粒体不良的升高有关,导致线粒体膜势下降。 14-3-3蛋白通常与Akt磷酸化不良相互作用,从而防止其易于迁移到线粒体,其中可以促进细胞死亡。姜黄素不仅降低了14-3-3蛋白的表达,而且促进了依赖于Akt依赖的方式的不良磷酸化。我们的结果为姜黄素在线粒体级联的多个阶段提供了姜黄素的新探测。

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