Department of Nutritional Science, Fu Jen Catholic University , New Taipei City 24205, Taiwan.
J Agric Food Chem. 2014 Mar 5;62(9):2085-95. doi: 10.1021/jf4037722. Epub 2014 Feb 24.
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 G1 cell cycle arrest was observed in a dose-dependent treatment after H1299 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 D1, and cyclin D3 were decreased, although cyclin E and cyclin-dependent kinase 6 (CDK6) were increased in garcinol-treated H1299 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 G1 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 G1 population cells. Co-treatment with p38-MAPK inhibitor and garcinol synergistically elevated cyclin E, p21(Waf1/Cip1), and p27(Kip1) 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 G1 cell cycle arrest and apoptosis in lung cancer cells under different p53 statuses. The p53-independent G1 cell cycle arrest induced by garcinol might be through upregulation of p21(Waf1/Cip1) triggered from p38-MAPK signaling inactivation.
姜黄素,一种多异戊二烯基二苯并酮,来自藤黄果皮,具有抗炎、抗氧化、抗增殖和抗癌活性。然而,姜黄素在肺癌中的抗癌机制仍不清楚。因此,我们研究了姜黄素对人肺癌细胞增殖的抑制作用。用姜黄素处理 24 小时后,在剂量和时间依赖性方式下观察到 H460(野生型 p53)和 H1299(p53 缺失)细胞的形态变化和增殖抑制。此外,H1299 细胞暴露于姜黄素后,在剂量依赖性处理中观察到明显的 G1 细胞周期停滞,而姜黄素诱导 H460 细胞凋亡而不是细胞周期停滞。此外,在姜黄素处理的 H1299 细胞中,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,尽管细胞周期蛋白 E 和细胞周期蛋白依赖性激酶 6(CDK6)增加。同时,姜黄素处理后,CDK 抑制剂 p21(Waf1/Cip1)和 p27(KIP1)的蛋白水平也呈上调趋势。在姜黄素处理的细胞中,p21(Waf1/Cip1)与 CDK4/2 之间的蛋白结合水平增强,而 p27(KIP1)与 CDK4/2 之间的蛋白结合水平增强。此外,用特异性 siRNA 敲低 p21(Waf1/Cip1)可有效地防止姜黄素诱导的 G1 期阻滞。此外,姜黄素还以时间依赖性方式抑制 ERK 和 p38-MAPK 的激活。p38-MAPK 抑制剂预处理而非 ERK 抑制剂可增加姜黄素诱导的 G1 期细胞群。p38-MAPK 抑制剂和姜黄素共同处理可协同上调 cyclin E、p21(Waf1/Cip1)和 p27(Kip1)的表达。同时,过表达显性负性 p38-MAPK 也可增强 H1299 细胞中姜黄素诱导的 p21(Waf1/Cip1)表达。因此,我们的数据表明,姜黄素在不同 p53 状态下诱导肺癌细胞 G1 细胞周期阻滞和凋亡。姜黄素诱导的 p53 非依赖性 G1 细胞周期阻滞可能是通过 p38-MAPK 信号失活触发的 p21(Waf1/Cip1)上调。