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Ursolic Acid Triggers Apoptosis in Human Osteosarcoma Cells via Caspase Activation and the ERK1/2 MAPK Pathway

机译:熊果酸通过半胱天冬酶激活和ERK1 / 2 MAPK途径触发人骨肉瘤细胞凋亡

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Ursolic acid (UA), a naturally occurring pentacyclic triterpene acid found in many medicinal herbs and edible plants, has been shown to trigger apoptosis in several lines of tumor cells in vitro. We found that treatment with UA suppressed the viability of human osteosarcoma MG-63 cells and induced cell cycle arrest at sub-G1 and G2/M phases. Furthermore, exposure to UA induced intracellular oxidative stress and collapse of mitochondrial membrane permeability, resulting in the subsequent activation of apoptotic caspases 8, 9, and 3 as well as PARP cleavage, and ultimately apoptosis in MG-63 cells. Moreover, protein analysis of mitogen-activated protein kinase (MAPK)-related protein expression showed an increase in activated ERK1/2, JNK, and p38 MAPK in UA-treated MG-63 cells. In addition, UA-induced apoptosis was significantly abolished in MG-63 cells that had been pretreated with inhibitors of caspase 3, 8, and 9 and ERK1/2. Furthermore, UA-treated MG-63 cells also exhibited an enhancement in Bax/Bcl-2 ratio, whereas anti-apoptotic XIAP and survivin were down-regulated. Taken together, we provide evidence demonstrating that UA mediates caspase-dependent and ERK1/2 MAPK-associated apoptosis in osteosarcoma MG-63 cells.
机译:熊果酸(UAs)是在许多草药和食用植物中发现的天然存在的五环三萜酸,已被证明可在体外诱导几系肿瘤细胞凋亡。我们发现用UA治疗会抑制人骨肉瘤MG-63细胞的活力,并诱导亚G1和G2 / M期细胞周期停滞。此外,暴露于UA会诱导细胞内氧化应激和线粒体膜通透性的破坏,导致随后凋亡的胱天蛋白酶8、9和3活化以及PARP裂解,最终导致MG-63细胞凋亡。此外,对丝裂原激活的蛋白激酶(MAPK)相关蛋白表达的蛋白分析表明,UA处理的MG-63细胞中激活的ERK1 / 2,JNK和p38 MAPK增加。此外,UA-诱导的凋亡在已经用胱天蛋白酶3、8、9和ERK1 / 2抑制剂预处理的MG-63细胞中被显着消除。此外,UA处理的MG-63细胞还表现出Bax / Bcl-2比的增强,而抗凋亡的XIAP和survivin被下调。两者合计,我们提供的证据表明,UA介导骨肉瘤MG-63细胞中caspase依赖性和ERK1 / 2 MAPK相关的凋亡。

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