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A novel polysaccharide from Sargassum integerrimum induces apoptosis in A549 cells and prevents angiogensis in vitro and in vivo

机译:一种新的羊栖菜多糖在体外和体内诱导A549细胞凋亡并阻止血管生成

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Many polysaccharides isolated from plants have exhibited promising antitumor activities. The aim of this study is to investigate the antitumor activity of the novel polysaccharide named SPS from Sargassum integerrimum, elucidate the underlying anticancer mechanism in a human lung cancer cell line A549, and evaluate its anti-angiogenic activity both in vitro and in vivo. The results show that SPS significantly reduces A549 cells viability in a dose- and time-dependent manner via MTT method. Flow cytometry analysis indicates that SPS could induce cell apoptosis, the loss of mitochondrial membrane potential (MMP), generation of reactive oxygen species (ROS) and G2/M phase cell cycle arrest of A549 cells. Up-regulation of the expressions of P53 and Bax, down-regulation of the expression of Bcl-2, and activation of cleaved caspase-3, caspase-9 and PARP are also detected by western blotting after the treatment of SPS. In addition, SPS inhibits the proliferation, migration and cord formation of human umbilical vein endothelial cells (HUVECs) in vitro, and prevents the vascular development of zebrafish embryos in vivo. Altogether, our data prove the anticancer and anti-angiogenesis properties of SPS, and provide further insights into the potential pharmacological application of SPS as antitumor and anti-angiogenic agent against lung cancer.
机译:从植物中分离出的许多多糖均显示出有希望的抗肿瘤活性。这项研究的目的是研究新型的Sargassum integerrimum多糖的抗肿瘤活性,阐明在人肺癌细胞A549中的潜在抗癌机制,并评估其在体内和体外的抗血管生成活性。结果表明,通过MTT方法,SPS以剂量和时间依赖性方式显着降低A549细胞的活力。流式细胞仪分析表明,SPS可以诱导A549细胞凋亡,线粒体膜电位(MMP)丢失,活性氧(ROS)生成和G2 / M期细胞周期阻滞。 SPS处理后,还可以通过蛋白质印迹检测到P53和Bax表达的上调,Bcl-2表达的下调以及裂解的caspase-3,caspase-9和PARP的激活。此外,SPS在体外抑制人脐静脉内皮细胞(HUVEC)的增殖,迁移和脐带形成,并在体内阻止斑马鱼胚胎的血管发育。总而言之,我们的数据证明了SPS的抗癌和抗血管生成特性,并为SPS作为肺癌的抗肿瘤和抗血管生成剂的潜在药理应用提供了进一步的见解。

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