首页> 外文期刊>Journal of Agricultural and Food Chemistry >Induction of p21~(Waf1/Cip1) by Garcinol via Downregulation of p38-IVIAPK Signaling in p53-lndependent HI299 Lung Cancer
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Induction of p21~(Waf1/Cip1) by Garcinol via Downregulation of p38-IVIAPK Signaling in p53-lndependent HI299 Lung Cancer

机译:大蒜素通过下调p38-IVIAPK信号转导p53〜HIVI肺癌诱导p21〜(Waf1 / Cip1)

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摘要

Garcinol, a polyisoprenylated benzophenone, from Garcinia indica fruit rind has possessed anti-inflammatory, antioxidant, antiproliferation, and anticancer activities. However, the anticancer mechanisms of garcinol in lung cancer were still unclear. Therefore, we examine the effects of garcinol on antiproliferation in human lung cancer cells. Treatments with garcinol for 24 h exhibited morphological changes and inhibited the proliferation of H460 (p53-wild type) and H1299 (p53-null) cells in dose-and time-dependent manners. Furthermore, a significant Gl cell cycle arrest was observed in a dose-dependent treatment after HI299 cells were exposed in garcinol, whereas garcinol induced apoptosis rather than cell cycle arrest in H460 cells. Moreover, cyclin-dependent kinase 2 (CDK2), cyclin-dependent kinase 4 (CDK4), Cyclin Dl, and cyclin D3 were decreased, although cyclin E and cyclin-dependent kinase 6 (CDK6) were increased in garcinol-treated HI299 cells. Meanwhile, the protein levels of CDK inhibitors p21~(Waf1/Cip1) and p27~(kip1) also exhibited upregulation after garcinol treatments. The enhanced protein-associated level between p21~(Waf1/Cip1) and CDK4/2 rather than p27~(kip1) and CDK4/2 was demonstrated in garcinol-treated cells. Additionally, knock-down p21~(Waf1/Cip1) by specific siRNA competently prevented garcinol-induced Gl arrest. Besides, garcinol also inhibited ERK and p38-MAPK activations in time-dependent mode. The pretreatment with p38-MAPK inhibitor but not ERK inhibitor raised garcinol-induced Gl population cells. Co-treatment with p38-MAPK inhibitor and garcinol synergistically elevated cyclin E, p21~(Waf1/Cip1) and p27~(kip1)l expressions. Meanwhile, overexpression dominant negative p38-MAPK also enhanced garcinol-induced p21~(Waf1/Cip1) expression in H1299 cells. Accordingly, our data suggested that garcinol induced Gl cell cycle arrest and apoptosis in lung cancer cells under different p53 statuses. The p53-independent Gl cell cycle arrest induced by garcinol might be through upregulation of p21~(Waf1/Cip1) triggered from p38-MAPK signaling inactivation. Kgarcinol;; lung cancer;; pS3;; Gl arres;; p21~(Waf1/Cip1);; p38-MAPK
机译:藤黄果皮中的聚异戊二烯基二苯甲酮藤黄醇具有抗炎,抗氧化,抗增殖和抗癌的作用。然而,garcinol在肺癌中的抗癌机制仍不清楚。因此,我们检查了藤黄酚对人肺癌细胞抗增殖的影响。大蒜素处理24 h表现出形态变化,并以剂量​​和时间依赖性方式抑制H460(p53野生型)和H1299(p53无细胞)细胞的增殖。此外,在将HI299细胞暴露于garcinol中之后,在剂量依赖性治疗中观察到显着的G1细胞周期停滞,而garcinol诱导细胞凋亡而不是H460细胞中的细胞周期停滞。此外,尽管在经菊酯处理的HI299细胞中细胞周期蛋白E和细胞周期蛋白依赖性激酶6(CDK6)增加,细胞周期蛋白依赖性激酶2(CDK2),细胞周期蛋白依赖性激酶4(CDK4),细胞周期蛋白D1和细胞周期蛋白D3减少。同时,经花椒素处理后,CDK抑制剂p21〜(Waf1 / Cip1)和p27〜(kip1)的蛋白水平也有上调。在用大蒜油处理的细胞中,p21〜(Waf1 / Cip1)和CDK4 / 2之间的蛋白相关水平增强,而不是p27〜(kip1)和CDK4 / 2之间的蛋白相关水平提高。此外,通过特异性siRNA敲低p21〜(Waf1 / Cip1)可以有效防止藤黄酚诱导的Gl阻滞。此外,大蒜素还以时间依赖性方式抑制ERK和p38-MAPK活化。用p38-MAPK抑制剂而不是ERK抑制剂进行的预处理提高了藤黄酚诱导的G1群体细胞。与p38-MAPK抑制剂和藤黄素共同处理可协同提高细胞周期蛋白E,p21〜(Waf1 / Cip1)和p27〜(kip1)l的表达。同时,过表达的显性负性p38-MAPK也增强了藤黄酚诱导的H1299细胞中p21〜(Waf1 / Cip1)的表达。因此,我们的数据表明在不同的p53状态下,藤黄酚诱导肺癌细胞中的G1细胞周期停滞和凋亡。藤黄酚诱导的不依赖p53的G1细胞周期阻滞可能是由于p38-MAPK信号失活触发的p21〜(Waf1 / Cip1)上调所致。甘醇;;肺癌; pS3 ;; gl arres ;; p21〜(Waf1 / Cip1);; p38-MAPK

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