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首页> 外文期刊>International journal of oncology >Anticancer activity of a synthetic peptide derived from harmoniasin, an antibacterial peptide from the ladybug Harmonia axyridis
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Anticancer activity of a synthetic peptide derived from harmoniasin, an antibacterial peptide from the ladybug Harmonia axyridis

机译:源自谐和素的合成肽的抗癌活性,谐和素是瓢虫Harmonia axyridis的抗菌肽

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Harmoniasin is a defensin-like antimicrobial peptide identified from the ladybug Harmonia axyridis. Among the synthetic homodimer peptide analogues derived from harmoniasin, HaA4 has been found to have antibacterial activity without hemolytic activity. In this study, we investigated whether HaA4 has anticancer activity against human leukemia cell lines such as U937 and Jurkat cells. HaA4 manifested cytotoxicity and decreased the cell viability of U937 and Jurkat cells in MTS assay and LDH release assay. We found that HaA4 induced apoptotic and necrotic cell death of the leukemia cells using flow cytometric analysis, acridine orange/ethidium bromide staining and nucleosomal fragmentation of genomic DNA. Activation of caspase-7 and -9 and fragmentation of poly (ADP-ribose) polymerase was detected in the HaA4-treated leukemia cells, suggesting induction of a caspase-dependent apoptosis pathway by HaA4. Caspase-dependent apoptosis was further confirmed by reversal of the HaA4-induced viability reduction by treatment of Z-VAD-FMK, a pan-caspase inhibitor. In conclusion, HaA4 caused necrosis and caspase-dependent apoptosis in both U937 and Jurkat leukemia cells, which suggests potential utility of HaA4 as a cancer therapeutic agent.
机译:Harmoniasin是一种从瓢虫Harmonia axyridis鉴定出的防御素样抗菌肽。在衍生自谐胺素的合成同型二聚体肽类似物中,HaA4具有抗菌活性而无溶血活性。在这项研究中,我们调查了HaA4是否对人类白血病细胞系(例如U937和Jurkat细胞)具有抗癌活性。在MTS试验和LDH释放试验中,HaA4表现出细胞毒性并降低U937和Jurkat细胞的细胞活力。我们发现HaA4使用流式细胞仪分析,a啶橙/溴化乙锭染色和基因组DNA的核小体片段化诱导了白血病细胞的凋亡和坏死细胞死亡。在经HaA4处理的白血病细胞中检测到caspase-7和-9的激活以及多聚(ADP-核糖)聚合酶的断裂,这表明HaA4诱导了caspase依赖性凋亡途径。通过逆转HaA4诱导的活力的降低,进一步证实了胱天蛋白酶依赖性细胞凋亡,HaA4诱导的活力降低是通过泛胱天蛋白酶抑制剂Z-VAD-FMK的治疗实现的。总之,HaA4在U937和Jurkat白血病细胞中引起坏死和caspase依赖性凋亡,这表明HaA4作为癌症治疗剂的潜在用途。

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