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Anticancer Activity of Anthopleura anjunae Oligopeptides in Prostate Cancer DU-145 Cells

机译:安牛按蚊寡肽对前列腺癌DU-145细胞的抗癌活性

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摘要

Anthopleura anjunae anti-tumor peptide (AAP-H) is a pentapeptide from the sea anemone Anthopleura anjunae with an amino acid sequence of Tyr-Val-Pro-Gly-Pro that is obtained by alkaline protease enzymatic hydrolysis extraction. In this study, we investigated the inhibitory effects of AAP-H on prostate cancer DU-145 cell proliferation using a methylthiazolyldiphenyl-tetrazolium bromide assay. Cell morphology was analyzed by hematoxylin-eosin staining, acridine orange/ethidium bromide fluorescence staining, Hoechst 33258 fluorescence staining, and scanning electron microscopy. The mitochondrial membrane potential was determined by flow cytometry following JC-1 staining. The cell apoptosis rate was measured by Annexin V-fluorescein isothiocyanate and propidium iodide staining followed by flow cytometric analysis, and the expression of apoptosis-associated proteins was assayed by Western blotting. The results demonstrated that AAP-H induced significant reductions in the number of viable cells and increased cell death in both a dose-dependent and time-dependent manner, with an IC50 of approximately 9.605 mM, 7.910 mM, and 2.298 mM at 24 h, 48 h, and 72 h, respectively. The morphologic characteristics of apoptotic cells were observed after treatment with AAP-H. The mitochondrial membrane potential was markedly decreased, and apoptosis increased after AAP-H treatment. Pro-apoptotic proteins, such as Bax, cytochrome-C, caspase-3, and caspase-9 were increased, but Bcl-2 was decreased. These findings suggest that AAP-H has moderate inhibitory effects on prostate cancer DU-145 cells, and the mechanism might involve the mitochondria-mediated apoptotic pathway. Therefore, AAP-H is a candidate anti-prostate cancer drug or health-care food.
机译:Anjunpleura anjunae抗肿瘤肽(AAP-H)是来自海葵Anthopleura anjunae的五肽,其氨基酸序列为Tyr-Val-Pro-Gly-Pro,可通过碱性蛋白酶酶解提取获得。在这项研究中,我们使用甲基噻唑基二苯基溴化四氮唑测定法研究了AAP-H对前列腺癌DU-145细胞增殖的抑制作用。通过苏木精-伊红染色,a啶橙/溴化乙锭荧光染色,Hoechst 33258荧光染色和扫描电子显微镜分析细胞形态。 JC-1染色后,通过流式细胞仪测定线粒体膜电位。通过膜联蛋白V-异硫氰酸荧光素和碘化丙啶染色,然后通过流式细胞术分析,测量细胞凋亡率,并通过蛋白质印迹法检测凋亡相关蛋白的表达。结果表明,AAP-H以剂量依赖和时间依赖两种方式诱导了活细胞数量的显着减少和细胞死亡的增加,在24 h时的IC50分别为9.605 mM,7.910 mM和2.298 mM,分别为48小时和72小时。用AAP-H处理后观察到凋亡细胞的形态特征。 AAP-H处理后,线粒体膜电位明显降低,凋亡增加。促凋亡蛋白,例如Bax,细胞色素C,caspase-3和caspase-9增加,而Bcl-2减少。这些发现表明,AAP-H对前列腺癌DU-145细胞具有中度抑制作用,其机制可能涉及线粒体介导的凋亡途径。因此,AAP-H是候选的抗前列腺癌药物或保健食品。

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