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Licochalcone A-induced human gastric cancer BGC-823 cells apoptosis by regulating ROS-mediated MAPKs and PI3K/AKT signaling pathways

机译:Licochalcone A通过调节ROS介导的MAPK和PI3K / AKT信号通路诱导人胃癌BGC-823细胞凋亡

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摘要

Both phosphatidylinositol 3-kinase (PI3K)/AKT and mitogen activated protein kinase (MAPK) signaling cascades play an important role in cell proliferation, survival, angiogenesis, and metastasis of tumor cells. In the present report, we investigated the effects of licochalcone A (LA), a flavonoid extracted from licorice root, on the PI3K/AKT/mTOR and MAPK activation pathways in human gastric cancer BGC-823 cells. LA increased reactive oxygen species (ROS) levels, which is associated with the induction of apoptosis as characterized by positive Annexin V binding and activation of caspase-3, and cleavage of poly-ADP-ribose polymerase (PARP). Inhibition of ROS generation by N-acetylcysteine (NAC) significantly prevented LA-induced apoptosis. Interestingly, we also observed that LA caused the activation of ERK, JNK, and p38 MAPK in BGC-823 cells. The antitumour activity of LA-treated BGC-823 cells was significantly distinct in KM mice in vivo. All the findings from our study suggest that LA can interfere with MAPK signaling cascades, initiate ROS generation, induce oxidative stress and consequently cause BGC cell apoptosis.
机译:磷脂酰肌醇3-激酶(PI3K)/ AKT和有丝分裂原活化蛋白激酶(MAPK)信号级联在肿瘤细胞的细胞增殖,存活,血管生成和转移中均起着重要作用。在本报告中,我们研究了从甘草根中提取的类黄酮licochalcone A(LA)对人胃癌BGC-823细胞中PI3K / AKT / mTOR和MAPK活化途径的影响。 LA增加了活性氧(ROS)水平,这与细胞凋亡的诱导有关,其特征在于膜联蛋白V的阳性结合和caspase-3的活化,以及多聚ADP-核糖聚合酶(PARP)的裂解。 N-乙酰基半胱氨酸(NAC)抑制ROS生成可显着阻止LA诱导的细胞凋亡。有趣的是,我们还观察到LA导致BGC-823细胞中ERK,JNK和p38 MAPK激活。在KM小鼠体内,LA处理的BGC-823细胞的抗肿瘤活性明显不同。我们研究的所有发现表明,LA可以干扰MAPK信号级联反应,启动ROS生成,诱导氧化应激并因此导致BGC细胞凋亡。

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