首页> 美国卫生研究院文献>Marine Drugs >Selenium-Containing Polysaccharide-Protein Complex in Se-Enriched Ulva fasciata Induces Mitochondria-Mediated Apoptosis in A549 Human Lung Cancer Cells
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Selenium-Containing Polysaccharide-Protein Complex in Se-Enriched Ulva fasciata Induces Mitochondria-Mediated Apoptosis in A549 Human Lung Cancer Cells

机译:富硒Ul豆中含硒的多糖蛋白复合物诱导线粒体介导的A549人肺癌细胞凋亡。

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摘要

The role of selenium (Se) and Ulva fasciata as potent cancer chemopreventive and chemotherapeutic agents has been supported by epidemiological, preclinical, and clinical studies. In this study, Se-containing polysaccharide-protein complex (Se-PPC), a novel organoselenium compound, a Se-containing polysaccharide-protein complex in Se-enriched Ulva fasciata, is a potent anti-proliferative agent against human lung cancer A549 cells. Se-PPC markedly inhibited the growth of cancer cells via induction of apoptosis which was accompanied by the formation of apoptotic bodies, an increase in the population of apoptotic sub-G1 phase cells, upregulation of p53, and activation of caspase-3 in A549 cells. Further investigation on intracellular mechanisms indicated that cytochrome C was released from mitochondria into cytosol in A549 cells after Se-PPC treatment. Se-PPC induced depletion of mitochondrial membrane potential (ΔΨm) in A549 cells through regulating the expression of anti-apoptotic (Bcl-2, Bcl-XL) and pro-apoptotic (Bax, Bid) proteins, resulting in disruption of the activation of caspase-9. This is the first report to demonstrate the cytotoxic effect of Se-PPC on human cancer cells and to provide a possible mechanism for this activity. Thus, Se-PPC is a promising novel organoselenium compound with potential to treat human cancers.
机译:流行病学,临床前和临床研究支持了硒(Se)和筋膜Ulva fasciata作为有效的化学预防和化学治疗剂的作用。在这项研究中,含硒的多糖蛋白复合物(Se-PPC)是一种新型的有机硒化合物,富含硒的Ulva fasciata中的含硒的多糖蛋白复合物是一种有效的抗人肺癌A549细胞的抗增殖剂。 。 Se-PPC通过诱导凋亡显着抑制癌细胞的生长,并伴随凋亡小体的形成,凋亡性亚G1期细胞群的增加,p53的上调以及A549细胞中caspase-3的激活。对细胞内机制的进一步研究表明,Se-PPC处理后,细胞色素C从线粒体释放到A549细胞的胞质溶胶中。 Se-PPC通过调节抗凋亡蛋白(Bcl-2,Bcl-XL)和促凋亡蛋白(Bax,Bid)的表达诱导A549细胞线粒体膜电位(ΔΨm)耗竭,从而破坏了A549细胞的活化caspase-9。这是第一个证明Se-PPC对人癌细胞的细胞毒性作用并为该活性提供可能机制的报道。因此,Se-PPC是一种有前途的新型有机硒化合物,具有治疗人类癌症的潜力。

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