首页> 外文期刊>Journal of Agricultural and Food Chemistry >Induction of Human-Lung-Cancer-A549-Cell Apoptosis by 4-Hydroperoxy-2-decenoic Acid Ethyl Ester through Intracellular ROS Accumulation and the Induction of Proapoptotic CHOP Expression
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Induction of Human-Lung-Cancer-A549-Cell Apoptosis by 4-Hydroperoxy-2-decenoic Acid Ethyl Ester through Intracellular ROS Accumulation and the Induction of Proapoptotic CHOP Expression

机译:通过细胞内ROS累积和促进凋亡斩波表达的4-硫烷-2-癸烯酸乙酯诱导人肺癌-A549细胞凋亡

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Royal jelly, a natural product secreted by honeybees, contains several fatty acids, such as 10-hydroxy-2-decenoic acid (DE), and shows anti- and pro-apoptotic properties. 4-Hydroperoxy-2-decenoic acid ethyl ester (HPO-DAEE), a DE derivative, exhibits potent antioxidative activity; however, it currently remains unclear whether HPO-DAEE induces cancer-cell death. In the present study, treatment with HPO-DAEE induced human-lung-cancer-A549-cell death (52.7 +/- 10.2%) that was accompanied by DNA fragmentation. Moreover, the accumulation of intracellular reactive oxygen species (ROS, 2.38 +/- 0.1-fold) and the induction of proapoptotic CCAAT-enhancer-binding-protein-homologous-protein (CHOP) expression (18.4 +/- 4.0-fold) were observed in HPO-DAEE-treated cells. HPO-DAEE-elicited CHOP expression and cell death were markedly suppressed by pretreatment with N-acetylcysteine (NAC), an antioxidant, by 2.40 +/- 1.57-fold and 5.7 +/- 1.6%, respectively. Pretreatment with 4-phenylbutyric acid (PBA), an inhibitor of endoplasmic reticulum stress, also suppressed A549-cell death (38.4 +/- 1.1%). Furthermore, we demonstrated the involvement of extracellular-signal : regulated protein kinase (ERK) and p38-related signaling in HPO-DAEE-elicited cell-death events. Overall, we concluded that HPO-DAEE induces A549-cell apoptosis through the ROS-ERK-p38 pathway and, at least in part, the CHOP pathway.
机译:蜂蜜果冻是蜜蜂分泌的天然产物,含有几种脂肪酸,例如10-羟基-2-癸烯酸(DE),并显示出抗凋亡性质。 4-二氢氧基-2-癸烯酸乙酯(HPO-DAEE),DE衍生物,表现出有效的抗氧化活性;但是,它目前尚不清楚HPO-DAEE是否诱导癌细胞死亡。在本研究中,用HPO-DAEE诱导人肺癌-A549细胞死亡(52.7 +/- 10.2%)伴随着DNA碎片。此外,细胞内反应性氧(ROS,2.38 +/- 0.1倍)的积累和诱导凋亡CCAAT-Enhancer结合蛋白 - 同源蛋白(Chec)表达(18.4 +/- 4.0倍)在HPO-DAEE治疗的细胞中观察到。通过用N-乙酰半胱氨酸(NaC),抗氧化剂,抗氧化剂,分别为2.40 +/- 1.57倍和5.7 +/- 1.6%,显着抑制了HPO-Daee-引发的Chec表达和细胞死亡。用4-苯基丁酸(PBA)的预处理,内质网胁迫抑制剂,也抑制了A549细胞死亡(38.4 +/- 1.1%)。此外,我们证明了细胞外信号的参与:调节蛋白激酶(ERK)和P38相关信号在HPO-DAEE-引发的细胞死亡事件中。总体而言,我们得出结论,HPO-DAEE通过ROS-ERK-P38途径诱导A549细胞凋亡,并且至少部分地是印缩途径。

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